Caffeine Blues
Bking 35 mg.
_____
chocolate per ounce
small candy 25 mg.
_____
bar per bar
Total Daily Caffeine Intake _____
YOUR CAFFEINE QUOTIENT
The fight-or-flight response was designed for stress that was episodic. Everything was fine, then
there was a tiger, our adrenals pumped out epinephrine, and we ran like the dickens. Today,
however, stress tends to be chronic, and when you consider that most people typically consume
caffeine at regular intervals during the day, you begin to understand the magnitude of the problem.
Our bodies are in a constant state of “emergency alert,” and the results can be devastating.
For most of us, the appropriate response to stress is not fight or flight at all. You may be sitting
at a desk or driving in your car when the stress mechanism is triggered. If that’s the case, the sugar
and fat that are dumped into your bloodstream go unused. The sugar creates additional metabolic
stress, and the fat clogs your arteries. Your muscles tense, but to no useful purpose (after all, you can
only grip the steering wheel so hard). And since blood flow has been diverted from the
gastrointestinal tract, the food you just ate is converted to a fermenting and putrefying mass.
CAFFEINE IMPAIRS DIGESTION
Impaired digestion is more of a problem than most people realize—and it gets worse with caffeine
(see Chapter 5). That jumbo thirty-two-ounce soft drink or the double espresso we have with meals
is a major contributor to the bloating, pain, and gas that roughly 50 percent of American adults
experience after they eat. And these symptoms are only the physical signs of maldigestion. Unseen
are the harmful by-products of fermentation and putrefaction. Some of these by-products are
absorbed back into the bloodstream, and the toxins that stay in the gut increase your risk of
gastrointestinal disease.
David Morgan, director of the University of South Florida’s Institute on Aging, puts stress-
induced maldigestion into an evolutionary perspective when he states, “There’s no reason to digest
your breakfast if you are about to become lunch.… [Under stress] a whole series of maintenance
and repair activities just stop.”13
CAFFEINE’s ICY GRIP
Have you ever noticed your fingers getting cold after a cup of coffee? That’s another part of the
stress response known as vascular resistance, in which peripheral blood vessels constrict. This
response is great if you’re fighting for your life—if you’re cut, you’ll lose less blood and your blood
will clot faster. But if you’re sitting at breakfast reading the morning paper, vascular resistance will
only raise your blood pressure and significantly increase your chances of having a heart attack or
stroke.
Of course, vascular resistance affects blood vessels throughout the body, not just in your
fingertips. The coldness in your hands and feet indicates that billions of cells are suffering from
reduced metabolic efficiency. That means less oxygen is getting to those cells and less carbon
dioxide and other wastes are being removed. It means that fine blood vessels in the brain are
constricting and cerebral blood flow is reduced. And because caffeine increases brain activity at the
same time, a situation known as relative brain hypoperfusion results.14 In this condition, the brain is
deprived of oxygen, and the consequences, when repeated day after day, can be quite serious.
Critical Point #4: Cortisol, the Long Burn
Epinephrine, it turns out, is only half the story. With daily caffeine use, another stress hormone
known as cortisol becomes elevated.15 The important thing to remember about cortisol is that it
tends to remain in the bloodstream much longer than epinephrine or norepinephrine. In fact, people
who consume more than 300 milligrams of caffeine per day may have elevated serum cortisol for
eighteen out of every twenty-four hours. And that sets them up for countless health problems.
You don’t really “feel” cortisol the way you feel adrenaline. It’s hard to pinpoint exactly what’s
wrong, and after a while, most people don’t even realize that they’re different. The quality of their
sleep is diminished, their immune system is adversely affected, age-related deterioration is
accelerated, and there is a gradual but significant change in mind, mood, and behavior.
One client who kicked the caffeine habit recently told me, “It’s as though a cloud has been lifted
from my body and mind. I had no idea that I was such an angry and frustrated person.” That’s
because cortisol has a powerful effect on personality.
Critical Point #5: Your Dopamine Levels
As neurobiologists unravel the mechanism of addiction, it becomes more and more clear that not
only is caffeine addictive, but it also encourages other addictions to substances like nicotine. The
key factor in this interaction appears to be a brain chemical known as dopamine.
Dopamine belongs to a class of biochemicals known as neurotransmitters. As the name implies,
these remarkable substances, produced by the brain and nervous system, help control the
transmission of information from neuron to neuron. Some neurotransmitters (called excitory neuro-
transmitters) speed up this information exchange. Inhibitory neurotransmitters slow neuron firing.
But these biochemicals do not merely control the speed of the brain; they also affect (some
would even say determine) our feelings. They are therefore a powerful influence on behavior.
Dopamine is associated with feelings of pleasure and elation, and scientists now believe that all
addiction involves the ability of a substance to raise dopamine levels in the brain. Some substances,
like amphetamines, do this by stimulating the brain to release greater amounts of dopamine, while
cocaine and others block the brain’s ability to clear dopamine from nerve endings. Either way,
greater amounts of dopamine are available to stimulate receptor sites in the brain, thus producing the
drug high.
In May 1997, Time magazine ran a cover story on addiction and listed caffeine with other
addictive drugs. But they only stated that caffeine “may trigger release of dopamine.” 16 In reality,
the evidence for the caffeine-dopamine connection is unquestionable. A decade ago, scientists
confirmed that caffeine raises dopamine levels. One study even noted that the mechanism by which
this occurs is “similar to that observed during amphetamine administration.”17 In the last two years
no less than twenty-six scientific studies have described the ways that caffeine interacts with
dopamine to alter feelings and behavior. Research shows that caffeine also interacts with opiate
receptors, and this may very well strengthen the addictive quality of the compound.18
Now, I know what you’re thinking. There’s no comparison between coffee and opium, cocaine,
and amphetamines. Those drugs drive people to destructive behavior, while coffee merely produces
a sense of stimulation. But that is precisely the point. We now know that all of these drugs act along
similar biochemical pathways, in the same areas of the brain. It turns out that there is a continuum of
addiction, and just because one substance is incredibly harmful does not mean that we should ignore
other substances that are only moderately harmful. Moreover, it is not just the positive dopamine
and adrenal stimulation that coffee drinkers are after. As in all truly addictive behaviors, coffee and
cola drinkers need their fix in order to avoid the negative experiences of headache, fatigue,
irritability, and depression.
Caffeine in some form is consumed by nearly 200 million Americans every day. The harmful
effects of this drug are extremely well documented. It’s time we all woke up to the truth about the
addictive nature of caffeine, as well as its potential for great bodily and mental harm.
The good news is that you can free yourself from caffeine addiction by using the clinically
tested Off the Bean program presented in Chapter 10. And if facing life caffeine free is too
frightening a thought, rest assured that you will find many healthful suggestions for increasing your
own natural energy and restoring your adrenals and nervous system.
BUT WHERE WILLI GET THE ENERGY?
The fact is that caffeine never gave you energy. It stimulated your nervous system and adrenals, and
that’s not energy, it’s stress. To get this point across to my clients, I ask them to imagine going to a
bank for a loan. The loan officer is superfriendly and readily agrees. But as you’re leaving the bank,
you read the fine print, which lists the interest rate at 75 percent! Would you be interested in such a
loan? Likewise, the “energy” you receive from caffeine is really just a loan from your adrenals and
liver, and the interest is extremely high. At some point (referred to as adrenal exhaustion) you may
find yourself “bankrupt” and unable to repair the damage.
Stress—and by that I mean unresolved or unmanaged stress (perhaps more properly called
distress)—is a silent saboteur of health. Every day, 1 million Americans are absent from work
because of stress-related disorders. Experts agree that stress is a factor in most diseases, and a major
factor in disorders such as anxiety, insomnia, depression, ulcers, rheumatoid arthritis, headache,
hypo-glycemia, asthma, herpes, hypertension, and heart disease. And yet, if you walk into most
hospital waiting rooms, you’ll find a coffee machine. Perhaps that’s because we don’t understand
how stress ruins our health. If you ask the average person, he or she will certainly tell you that stress
causes tension. He or she may even know that this tension can increase blood pressure and give you
headaches. But to make informed decisions about your caffeine intake, it’s important to know all the
facts—and in this case, it’s fairly easy, because they all relate to your adrenal glands.
Critical Point #6: Your Adrenal Glands: Overworked and Underpaid
You don’t gain much appreciation for the adrenal glands in physiology class. The focus is too much
on memorizing their structure and function. Besides, the adrenals are rather small (smaller than your
thumb) and easy to overlook (many anatomy charts don’t even include them). So it wasn’t until I
got into clinical practice that I realized how extremely important they are. I was seeing patients
every day with serious health problems that strong, healthy adrenals could have prevented. Why
were these people vulnerable to allergy, inflammation, hypertension, infection, and fatigue? What
was it that weakened their adrenals? To find the answer, you must learn something about these
amazing glands. (A discussion of specific disorders associated with adrenal dysfunction is found in
Chapter 5.)
The center of the adrenal gland, called the medulla, produces two major biochemicals:
epinephrine and nor-epinephrine. As I mentioned, these are the fight-or-flight hormones that create
the stress response listed in Illustration 1. But we need these hormones for more than the occasional
emergency. Epinephrine and norepinephrine are also required for any stressful activity, including
sports and recreation.
Surrounding the medulla is the adrenal cortex, which produces a variety of other hormones that
help regulate blood pressure, blood sugar, mineral levels, immune activity, inflammation, and cell
growth and repair. In all, more than 150 hormones are produced by the adrenals or metabolized from
adrenal hormones.
One group, known as glucocorticoids (including corti-sol), act as a brake on the immune
system. This is an essential function that prevents overenthusiastic immune cells from attacking the
body’s own healthy tissues. But scientists have recently learned that excess glucocorticoid
production (caused by stress and caffeine) can profoundly suppress immunity.19,20 The important
point to understand is that caffeine combined with emotional stress has been shown to raise
glucocorticoid production far more than either caffeine or stress alone.
Critical Point #7: Immunity and Aging
The vaccine response is one of the wonders of modern medicine. By exposing the body to a
weakened (or even dead) strain of a disease, the body “remembers” the enemy so that any future
encounter with the microbe will result in a swift and strong immune response. Obviously, the
effectiveness of a vaccine depends upon the production of these memory cells, called antibodies.
A research team led by Dr. Ronald Glaser gave a hepatitis vaccine to forty-eight students, half
of whom were in the midst of final exams (and drinking more coffee). A month later, it was found
that the students with elevated stress hormones developed the least protection (produced the lowest
number of antibodies) against hepatitis.21
But the stress-immune response is not always characterized by suppressed function. The other
side of the coin is called immune dysregulation, a condition in which the immune system attacks
healthy tissue. There is an intriguing but not fully understood connection between stress, caffeine,
and autoimmune disorders such as rheumatoid arthritis, lupus, and MS. Now we know that the onset
of autoimmune disease is very frequently preceded by a period of severe stress or depression, but
it’s not simply that stress weakens the adrenals and leads to poor immune control. Continued
research has led to a very exciting breakthrough related to another hormone known as DHEA.
THE DHEA CONNECTION
DHEA (dehydroepiandrosterone) can accurately be called the vitality hormone. The adrenals
produce it in abundance during youth, helping to create the energy, optimism, sex drive, and high
level of immunity we enjoy in our twenties. DHEA is the precursor to other essential sex and youth
hormones such as testosterone and estrogen. At about age twenty-five, DHEA levels start to drop,
and this decline continues until at age seventy, most people are only producing about 15 percent of
prime peak. The effects of low DHEA are unfortunate and far-reaching: decreased energy, decreased
immune competence, and immune dysregulation contributing to autoimmune disease. Low DHEA
obviously contributes to decreased sex drive, as well as reduced ability to repair and rebuild tissues.
Since such effects normally accompany aging, researchers thought the decline in DHEA
production was just one of the inevitable effects of growing old. As it turns out, however, decreased
DHEA production is also a cause of the aging process. In fact, some experts believe that declining
production of DHEA is not inevitable at all, but simply reflects the declining health of the adrenal
glands. Today, endocrinologists are using the term adrenopause to describe this phenomenon, and a
growing number of health professionals (including myself) believe that much of the degeneration
associated with aging can be avoided by maintaining high levels of DHEA. That, of course, is going
to be terribly difficult if you’re drinking a lot of coffee— since caffeine elevates cortisol, which
leads to DHEA deficiency.
WHAT CAUSES ADRENOPAUSE?
Again, it’s tempting simply to ascribe it to the aging process, but facts do not support that position.
Looking at a population of sixty-year-olds, you’ll find some with DHEA blood levels of 200
nanograms per deciliter and others with three times that amount. There are numerous factors that
contribute to the spread, but mainly it reflects the differing ability of human beings to withstand the
effects of stress.
Research is revealing that cortisol and DHEA, both produced in the adrenal cortex, hold an
inverse relationship. As serum cortisol increases, DHEA levels fall. It may be that stress and
caffeine create such a high need for cortisol that the exhausted adrenals simply cannot maintain
production of DHEA at optimal levels. This results in the double whammy of degeneration: elevated
cortisol and DHEA deficiency.
The importance of DHEA in maintaining peak immunity is clearly illustrated in the progression
of HIV infection to full-blown AIDS. In this case, deterioration is marked by declining levels of an
important immune cell known as the T helper (medical term: CD4 cell). Researchers have found a
striking correlation between blood levels of DHEA and CD4 counts of AIDS patients.22 The
investigators in one study stated, “There is a relationship between the circulating sex hormone
levels, particularly DHEA, and the progression of immune depression in HIV, whatever the risk
factor.” A 1996 editorial in the Journal of Laboratory and Clinical Medicine suggests that serum
DHEA be used as a marker for progression of HIV,23 and at least one clinical trial has found DHEA
supplementation to be effective in reducing the amount of HIV virus in the body.24
The important point for this discussion is that cortisol has been found to accelerate HIV
infection, while DHEA slows the virus down. There appears to be a “tug-of-war” in the bodies of
HIV-positive individuals between these two adrenal hormones. To the degree that cortisol wins, the
disease progresses. We would all do well to remember that this scenario is certainly not limited to
AIDS, but most likely plays a role in every disease we suffer.
Critical Point #8: Your Stress Threshold
Life is an unpredictable mix of pleasant and unpleasant events. Unpleasant events can be divided
into two categories: not getting what you want, and getting what you don’t want. Either can create
stress, but not necessarily dis tress, which suppresses immunity and increases risk for disease. The
determining factor is the individual’s emotional response to the event. Two people, for example, can
experience the same stressful situation (traffic ticket, final exam, fight with spouse), but one of them
is mildly annoyed while the other “flies off the handle” into distress. Psychologists look at this
response as part of the Type A/Type B personality picture, but they have failed to look at the
caffeine factor.
We now know that caffeine can lower the stress threshold (the point where stress becomes
distress) in virtually anyone, whether they are Type A, Type B, or anything in between. And the
amazing thing is that this “short-fuse” phenomenon occurs either when blood levels of caffeine rise,
or (in habitual coffee drinkers) when blood caffeine levels fall. One eye-opening study looked at
behavioral changes that occur when habitual coffee drinkers were deprived of their morning coffee.
Compared to controls, the coffee drinkers reacted to situational challenges with a far greater number
of negative mood effects, including anger, violence, frustration, and depression.25
CAFFEINE VERSUS GABA
As I mentioned, the brain uses adenosine receptors to keep neuron firing within safe limits.
Neurotransmitters comprise another very powerful control system. Remember that excitatory
neurotransmitters speed communication between neurons. The hormone norepinephrine is an
excitatory neurotransmitter that is stimulated by the ingestion of caffeine.
The primary inhibitory neurotransmitter is known as GABA, or gamma aminobutyric acid.
GABA has a unique ability to calm the mind without putting you to sleep. The researchers who
discovered GABA took mice and taught them to find their way through a maze. Once this was
accomplished, they stressed the mice by immobilizing them (mice hate that). Interestingly, the
stressed mice could no longer find their way through the maze. But when GABA was injected into
their brains, they waltzed right through. Seeing the obvious parallel between that experiment and the
way most of us live, other researchers scurried to their labs to synthesize GABA for human
consumption. This was accomplished in record time, and scant onths later, GABA appeared on the
shelves of health-food stores.
There are two reasons why I am telling you this story. First, it’s a good “nutrition detective”
lesson. In the mice study, the GABA was injected directly into the brain. The health-food store
products are oral capsules. As it turns out, you cannot raise brain levels of GABA by eating it. The
fragile molecule is completely digested in the stomach. So much for the idea of popping a few
GABA capsules with your double espresso.
The second point is that the mice research revealed yet another reason to decrease your intake of
coffee. Caffeine, it turns out, disrupts the normal metabolism of GABA.26 Here’s this wonderful
brain biochemical that increases the “filter mechanism” of the brain, helps you to step back and see
clearly even under stress, and caffeine screws it up. Thus, in the maze of life you never make it to
the cheese.
GABA IN YOUR GUT
New research tells us that GABA is also produced in the intestinal tract, where it serves a similar
purpose: calming anxiety and stress. Since caffeine disrupts the normal metabolism of GABA,
investigators now believe they have found the smoking gun to implicate coffee with ulcers and
irritable bowel syndrome. What’s more, this anti-GABA action is powerfully amplified by other
drugs, including commonly prescribed antibiotics. These medications interfere with the action of
GABA and at the same time decrease the body’s ability to detoxify caffeine.27 This combination can
produce anxiety, irritability, hyperactivi-ty, and even epilepsy-like convulsions28—all the more
reason to ask your physician if your medication has any interactions with caffeine.
RESEARCH CAPSULE
Habitual Caffeine Use Is No Protection
Coffee promoters are fond of claiming that the drug’s negative side effects
somehow “wear off” as you develop a tolerance to caffeine, but research does not
support that claim. In fact, major scientific reviews agree that, while the diuretic
effect may decrease with habitual use, humans do not develop “tolerance” to the far
more dangerous central nervous system effects.29–3031
Still, caffeine apologists can cite research where coffee drinkers were given
caffeine and their blood pressure did not increase. But this is not a real-world
experiment. In the real world, we are faced with numerous challenges as we go
through the day. Some of these challenges are mental (like taking a final exam),
some are emotional (dealing with a difficult relationship), and some are physical
(sports and exercise). Research with real people shows conclusively that caffeine
accelerates and magnifies the damage that we experience from stress. In fact, it is
often the critical factor that pushes us over the stress threshold into distress,
disease, and degeneration.
Here are three studies that debunk the idea that habitual coffee drinkers are
somehow immune to caffeine-induced stress damage. Note that all three are well-
designed, placebo-controlled experiments.
1. In this study, healthy students were selected to evaluate the combined
response to caffeine and a difficult laboratory task. All of the students were coffee
drinkers. Some were habitual consumers and others were light consumers. On the
test day, they were given a moderate dose of caffeine based on their weight. A 150-
pound man, for example, was given 238 milligrams, or the equivalent of a mug of
strong coffee.
Caffeine administration more than doubled epineph-rine and cortisol levels from
baseline, and the magnitude of this increase was not different between the habitual
and light coffee drinkers. The study authors concluded that: “Caffeine can
potentiate both cardiovascular and neuroendocrine stress reactivity, and the
habitual use of caffeine is not necessarily associated with the development of
tolerance to these effects.”
Source: J. D. Lane, R. A. Adoock, R. B. Williams et al., “Caffeine Effects on
Cardiovascular and Neuroendocrine Responses to Acute Psychosocial Stress and
Their Relationship to Level of Habitual Caffeine Consumption,” Psychosomatic
Medicine, May-June 1990;52(3):320-36.
2. Another study looked at the combination of caffeine and exercise. Again, the
subjects were healthy young men with normal blood pressure. This time the dose of
caffeine was even smaller, roughly the equiva lent of one mug of coffee.
We know that exercise by itself increases blood pressure, so measurements
were taken twice: once on the day when caffeine was administered and once on the
day when subjects received a placebo. Dangerous elevations of blood pressure
were recorded more than twice as often on caffeine days as compared to placebo
days. In addition, caffeine impaired circulation due to the constriction of blood
vessels and elevated stress hormones.
Source: B. H. Sung, W. R. Lovallo, G. A. Pincomb et al., “Effects of Caffeine on
Blood Pressure Response during Exercise in Normotensive Healthy Young Men,”
American Journal of Cardiology, April 1, 1990;63(13):909-13.
3. In the third study, students were given either caffeine (the equivalent of one mug
of coffee for a 150-pound person) or placebo during periods of low stress (no
exams) or high stress (final exams). Over a period of eight days, heart rate and
blood pressure were measured. As you would expect, the stress of exams
increased blood pressure slightly. But when caffeine was added, blood pressure
shot up in many of the subjects to the borderline hypertensive range. What’s more,
caffeine increased blood cortisol and cholesterol levels.
Source: G. A. Pincomb, W. R. Lovallo, R. B. Passey et al.; “Caffeine Enhances the
Physiological Response to Occupational Stress in Medical Students,” Health
Psychology, 1987;6(2):101-12.
Because this is a real-world scenario, this study brings up an important point. In the
real world, if a person were to go to the doctor with the symptoms created by
exams and caffeine, he or she would likely be placed on blood pressure medication
—which would be completely inappropriate and possibly dangerous. Do you think
doctors routinely survey their patients to determine caffeine ingestion? Did your
doctor ask you about caffeine at your last physical exam?
THE STRESS-FATIGUE-DISEASE CYCLE
It has been said that actions become habits and habits determine our lives. That is especially true
when it comes to what we eat and drink. The problem with the caffeine habit is that it’s very hard to
be moderate or even sensible. That’s because it sets up a cycle of alertness followed by fatigue. You
might start with one cup in the morning, but most people find that they soon need a second cup at
mid-morning, and another caffeine hit (coffee or cola) in the afternoon. Over time, adrenal weakness
leads to deeper fatigue, more caffeine, and a spiral of increasing stress and decreasing health that
can be devastating. The good news is that once you understand this cycle, you can break free. And
only when you break free you can begin the task of repairing the damage.
Illustration 2
The Stress-Fatigue-Disease Cycle
Clinical evidence suggests that at a certain point, stress and caffeine-induced alterations of
hormone and metabolic functions may not be reversable. The following case history will give you a
glimpse of how far this downward spiral can go.
Linda A. was a moderate coffee drinker until she started a very demanding job right after
college. Working long hours meant an additional mug of coffee around 3 P.M. that would keep her
going until six or seven. But the quality of her sleep began to suffer and, unlike her rise-and-shine
past, she found that she had to drag herself out of bed. She even had to move her alarm clock out of
reach to prevent herself from hitting the snooze button and being late for work. When she
complained about this to her doctor, he told her that the afternoon coffee was not likely to be
causing the insomnia and restlessness. He blamed it on the stress of her job.
As the months went on, however, she found that she could not function without two or three
cups of coffee in the morning. She looked forward to a 10 A.M. cup at work, and usually had a cola
beverage with lunch. Eventually, there was a steady stream of caffeine throughout her day; always a
mug of coffee or a can of cola at her desk. She started getting headaches, and the only thing that
seemed to help was a cup of coffee. She knew that she was, as she explained, “in trouble,” but she
thought she could hold everything together until things in her life “settled down.” Unfortunately,
that never happened. Instead, she came home one night and her husband announced that he was
leaving her.
He told her that her entire personality had changed since they met. She was no longer a fun-
loving, easygoing woman, but an irritable, anxious, and unhappy person She became defensive,
blaming the stress of her career. When he pointed out that their sex life was next to nonexistent, she
blamed her headaches and the fact that her periods literally knocked her out of commission for ten
days out of every month. She had never told him about the painful lumps in her breasts that made
intimacy a less than pleasurable experience.
The stress of her broken marriage got her to seek help, but all she received was a prescription
for a tranquilizer and an antidepressant. At the age of thirty-three, she started experiencing painful
swollen joints, but was given only painkillers.
Linda came to my office with the diagnosis of rheumatoid arthritis, cystic breast disease, PMS,
migraine, and depression. Her food and beverage survey revealed that she was ingesting over 1,000
milligrams of caffeine each day, and my suggestion that caffeine was causing many of her troubles
was at first met with disbelief and alarm. After all, she was convinced that without caffeine she
could not function. It was only after I showed her research proof associating caffeine with every one
of her disorders that she agreed to start cutting back. It took Linda four months to get down to two
cups of coffee per day, and at that point, she switched to tea.
After one year on my Off the Bean program, including nutritional therapy to help repair her
adrenals and nervous system, Linda was completely free of headaches. The painful lumps in her
breasts disappeared, her mood swings evened out, her energy dramatically improved, and her PMS
was a thing of the past. But three years later, she was still battling the arthritis. As her
rheumatologist explained, something in her body just went “haywire,” causing her immune system
to attack her joint tissue. Aside from steroid drugs and other powerful immune-suppressing agents,
he offered no hope for relief.
I believe that Linda will one day be free of rheumatoid arthritis, but it may take years. For so
long her body had been held in a perpetual state of near panic. Stress hormones ravaged her immune
system, destroyed muscle fibers, drove her DHEA levels down to those of a seventy-year-old, and
left her adrenals exhausted and weak. The road back is not easy, but she has seen tremendous
improvement.
By the way, Linda was using birth control pills when she first noticed that her sleep was
disturbed. These drugs decrease the body’s ability to detoxify caffeine, and as it turns out, that 3
P.M. mug of coffee was keeping caffeine coursing through her blood until 2 A.M. It was all
downhill from there.
Critical Point #9: Your Sleep Cycle
Few people understand the importance or the function of sleep. We tend to think of sleep as “wasted
time,” and that may be the reason why studies show that the vast majority of Americans don’t get
enough sleep. Pressed as we are for time, we just assume that we can get by with less. Even doctors
are largely unaware of the critical importance of sleep. They treat insomnia with drugs (many of
which actually disturb sleep quality), but few physicians today bother to take a sleep history.
Routine intake questionnaires rarely include a section on sleep habits.
But among researchers, sleep is an extremely hot topic. Entire journals are devoted to the
subject, and sleep centers are opening in research facilities around the world. This explosion of
interest has been fueled mainly by neurobiologists who are starting to unravel the complex way in
which the brain directs the healing powers of the body. And one of the most startling discoveries has
to do with what goes on while you sleep. When you begin to understand these mysteries, you’ll
never look at a cup of coffee in quite the same way. That’s because sleep can be a youth-restoring,
powerfully rejuvenating, deep healing experience—or, it can be merely a continuation of the day’s
tension, conflict, and frustration. For most of us, the difference is a drug called caffeine
The World Health Organization (WHO) in Geneva reports that more than 30 percent
of people in industrialized countries experience episodes of sleeplessness, and
about 12 percent of adults have chronic insomnia.
Source: A. La Voie, “Sleepless in Seattle, and All Around the Globe,” Medical
Tribune News Service, June 27, 1997.
As you may know, a night’s sleep is divided into roughly ninety-minute cycles in which brain
activity changes dramatically. In Illustration 3, you can see that during each cycle, the brain goes
through four stages, from S1 (shallow sleep) to S4 (deep sleep). Most people are familiar with Si
because that is when we dream and have rapid eye movement (REM). But in reality, each stage
provides the body and brain with essential repair, rejuvenate, and rebuild benefits. Dreams, for
example, are absolutely critical for maintaining mental and emotional health. We don’t know why,
but if you prevent a person from dreaming for just a few nights, that individual will start to
experience clear signs of psychosis. It was once thought that caffeine enhanced dream sleep, or at
least lengthened the S1 phase of the sleep cycle. But recent research shows that caffeine (and
numerous other drugs) can disrupt this crucial function.32
As important as dreams are to the mind, deep sleep (S4) is essential for the health of the body.
Interestingly, scientists have learned a great deal about deep sleep from studying coma patients. The
purpose of coma, you see, is to deactivate all nonessential functions of the body and brain in order
to devote every possible ounce of energy to the task of healing. Likewise, the body uses deep sleep
to mobilize all available resources for healing and rejuvenation. During S4 sleep, there is a massive
creation of new cells throughout the body. Every tissue benefits, but most activity is centered on
building immunity and restoring the nervous system. We all know how wonderful we feel after a
good night’s sleep. That’s because deep sleep provides a level of rest that cannot be obtained in any
other way. In a very restful night, you may experience deep sleep at two and possibly three phases.
But when there’s caffeine (or its metabolites) in your bloodstream, you are unlikely to experience
deep sleep at all.
Illustration 3
A Normal Sleep Cycle
Caffeine has been found to shorten total sleep time, increase the duration of Stage 2, shorten Stage
3, and often eliminate Stage 4 (deep sleep).
Sources: S. H. Onen, F. Onen, D. Bailly et al., “Prevention and Treatment of Sleep Disorders
through Regulation of Sleeping Habits,” Presse Medicale, 1994;12;23(10):485-89; and M. H.
Bonnet and D. L. Arand, “Metabolic Rate and Restorative Function of Sleep,” Physiology and
Behavior, April-May 1996;59(4-5):777-82.
Those who promote caffeine as a harmless drug like to cite research showing that coffee and
soft drink users become tolerant to the stimulant effects and no longer experience insomnia. You
must understand that insomnia is not the issue. Insomnia (the inability to fall asleep) deals only with
the quantity of sleep. The real issue here is sleep quality. Caffeine tolerance may allow you to fall
asleep, but if S4 sleep is disrupted, you will wake up feeling tired instead of renewed.
Research shows that people who consume more than 250 milligrams of caffeine per day tend to
have poor sleep quality.33,34 What’s more, they are generally unaware of this critical problem. In
one study, habitual coffee drinkers were allowed to drink coffee until midday (in order to prevent
withdrawal). Later in the day, they were given either caffeine or placebo, and on days when they
received placebo, their sleep quality improved significantly.35 As a result, they felt much better the
following day. But for millions of Americans, caffeine-induced sleep disorders remain hidden and
undiagnosed. These people drag themselves out of bed and remain tired through the day.
I don’t think it is being overly cynical to suggest that this is precisely what the caffeine industry
wants. After all, if you’re groggy in the morning, you’ll reach for their product. By midmorning,
that first cup will wear off, so you’ll reach for another. You’ll have a caffeine beverage with lunch
and most likely another in midafternoon—all because your body really didn’t rest. You fell asleep
but never got to experience the depth of sleep that you need most. Is the problem widespread?
Recent surveys suggest that 25 percent of U.S. adults have trouble falling asleep, 23 percent awaken
frequently, 25 percent wake up too early, nearly half of all Americans are dissatisfied with the
quality of their sleep, and one out of every ten is taking some medication to help them sleep.
While this certainly qualifies as an epidemic, I believe those numbers don’t come close to
identifying the magnitude of the sleep problem. That’s because we have limited information. In a
sleep laboratory, we’d be hooked up to a monitor that would record every stage of sleep on a device
called an electroencephalogram (EEG). The scientist conducting the study could tell us, “You never
made it into S4 sleep last night. Better cut back on the caffeine.” But in real life, most of us simply
look at the clock, wonder why we feel exhausted, and then stumble into the kitchen to make a pot of
coffee.
Take another look at Illustration 3. Did you notice that this normal sleep cycle takes place over a
span of eight hours? Do you normally get a full eight hours of sleep? I didn’t think so. In fact, few
American adults devote enough time to this critical repair and rebuild cycle, and we suffer greatly
for it.
CASE STUDY
Amy came to my office with a five-year history of fibromyalgia. During the interview, she was
surprised at how interested I was to know her caffeine history. In fact, no one had ever explained to
her the connection between caffeine and her painful disorder.
Now I believe that if you give a person enough time, he or she will usually tell you the cause of
their illness. Amy’s story was classic. She was a “one cup in the morning” woman with a low-stress
job in Thousand Oaks, California, a town about twenty-five miles north of Los Angeles. Life
changed dramatically for her when she landed the “job of her dreams” in LA. The commute was an
hour and a half on a good day, and to assure that she would not be late, Amy started leaving the
house at 6 A.M. That meant she had to get up at 5 A.M. sharp. Her usual bedtime (before the LA
job) was 11:30 or midnight, which gave her about seven hours of sleep, “barely enough” as she
described it.
But to get the same amount of sleep on her new schedule would mean going to bed at 10 P.M.
and she was just not tired at ten. In fact, if she went to bed at ten, she just tossed and turned until
midnight anyway, so she gave up and assumed that she could “catch up” on her sleep over the
weekends.
Unfortunately, it doesn’t work that way. It is possible to “make up” for one bad night’s sleep,
and maybe even two nights. But according to most sleep experts, after two consecutive nights of
poor sleep, the damage starts to accumulate. You’ll learn exactly how that damage contributes to
fibromyalgia in Chapter 5, but right now I want to tell you why Amy couldn’t fall asleep before
midnight. Actually, you probably already know.
Getting two hours’ less sleep made Amy tired, but she had to be “up” for her new job, so she
started drinking coffee while driving to LA. She bought a special “commuter mug” and didn’t notice
that it held twenty ounces, about twice what she normally drank. What’s more, she seldom had time
for her usual breakfast, and so this coffee was invariably consumed on an empty stomach. As the
weeks went by, she started having another mug of coffee at mid-morning and one or two cola
beverages in the afternoon. It wasn’t long before she started having shoulder and neck pain. Her
friends at work were quick to suggest that she get a better chair and elevate her wrists when using
the computer. She bought special back supports for the car seat and desk chair, and tried stretching
exercises twice a day, but the pain only got worse. That’s because none of these measures dealt with
the cause of her problem.
The trap that Amy was caught in is extremely common. You probably know someone with the
same story, and right now, it’s easy to see the elements of that cycle: reduced sleep led to increased
caffeine consumption, caffeine disrupted what little sleep Amy was able to get, and the loss of sleep
quantity and sleep quality contributed to her fibromyalgia, the primary symptoms of which are pain
and fatigue.
Illustration 4
The Caffeine-Sleep-Disease Cycle
Coffee and Sleep: Debunking More Myths
Time of Day
There is a popular notion that coffee before 3 P.M. can’t disturb your sleep. In fact, caffeine at any
time of the day can cause sleep problems, especially if you are under stress. Researchers at the
Institute of Pharmacology in Zurich, Switzerland, gave a moderate amount of caffeine (200
milligrams) to healthy subjects at 7 A.M. By 11 P.M. blood levels of caffeine had fallen more than
80 percent and still the subjects experienced significant sleep disturbance, especially in the S4
stage.36 This may be due to the stimulation of cortisol, or to some unidentified brain-body
dysfunction created by caffeine earlier in the day.
WHO’s MOST AT RISK?
We also tend to think that caffeine-related problems are mostly experienced by people in the
workforce. In reality, those hardest hit appear to be the elderly. Even though seniors tend to cut back
on coffee, the caffeine they do ingest is detoxified much more slowly and their nervous systems are
much more sensitive than those of younger people. Research is now showing that sleep disturbance
among the elderly is a major factor not only in age-related physical degeneration but in mental
degeneration as well.37, 38Investigators from the National Institute on Aging have identified another
culprit: hidden caffeine. Their 1995 report showed that those taking any caffeine-containing
medications were nearly twice as likely to have sleep problems compared to age-matched
controls.39 Avoiding these medications is not an easy task. Today, more than 2,000 OTC and
prescription medications contain caffeine.
Critical Point #10: Your Fatigue Quotient
While the connection between poor sleep and fatigue is obvious, caffeine contributes to fatigue in at
least three other ways. Adrenal exhaustion results in profound tiredness, as can blood sugar
abnormalities associated with caffeine use. And we’ve already seen in Chapter 2 (Test #4) that the
muscle tension resulting from stress can use up tremendous amounts of energy.
How ironic that the very substance people turn to for energy is a major cause of their fatigue. It
gets worse, of course, when you understand that the cumulative effect of fatigue and poor sleep is
more serious illness. In fact, fatigue is one of the top three reasons why Americans seek medical
help.40 In 1994, there were over 15 million doctor visits for this problem. The tragedy is that, for the
most part, physicians are unaware of the caffeine connection. Surveys show that fewer than 10
percent of patients receive advice from their doctor to reduce caffeine. Even with heavy coffee
drinkers, the percentage is less than 15 percent.41
The popular press, however, may be catching on. A while ago, U.S. News & World Report ran a
feature article on the growing epidemic of fatigue in America.42 Boxed out on page one of the
article was a list of “the most common causes of prolonged fatigue.” Caffeine addiction was number
two on the list, and, overall, caffeine was a factor in five of the seven points listed.
THE BLOOD SUGAR ROLLER COASTER
Hypoglycemia results when blood sugar levels fall below normal. Since blood sugar (or glucose) is
the fuel that runs our muscles and brain, hypoglycemia typically produces fatigue, depression, and
anxiety. There is no single cause of hypoglycemia. It is an imbalance in the complex process of
energy metabolism involving the liver, pancreas, and adrenal glands.
Caffeine plays a major role because it stimulates the fight-or-flight stress response described
earlier. As part of this response, the liver rapidly raises blood sugar levels. This is felt as a “lift” by
the person who drank the coffee (especially if the coffee contained added sugar) but the body must
then deal with the metabolic emergency of hyperglycemia (elevated blood sugar). This is
accomplished by the pancreas, which secrets insulin, driving the blood-sugar level down.
In some individuals, however, blood sugar may decrease to levels below normal, resulting in
hypoglycemia and the all-too-familiar “letdown” feeling a few hours after the coffee lift. Of course,
many people simply reach for another cup of coffee, which starts the roller-coaster cycle all over.
Although this model of “caffeinism” is well understood, it is not clear why some people are
more sensitive than others. Experts believe this has to do with the individual’s age, weight, body
composition, overall health, and other factors.
CASE STUDY
Jeff had a promising career as an architect. He worked in a huge Los Angeles firm, and competition
for advancement was fierce. When he came to see me, Jeff had been at the company for five years,
but his position was anything but secure. At any moment, he knew he could be replaced by an
ambitious and energetic intern. There were only two ways Jeff could demonstrate his value to the
firm: work harder and work longer. I was not surprised when he told me that he drank about twelve
cups of coffee a day.
At the age of thirty-four, Jeff was feeling old. He remembered a time, not so many years back,
when he would bounce out of bed in the morning, work hard, and still have energy to play softball
in the evening. As he sat talking to me, however, his manner was anything but bouncy. The dark
circles under his eyes told me that he was sleeping poorly. And although he had been a collegiate
All-American, I could tell that Jeff was out of shape and about twenty-five pounds overweight. At
his last physical, his doctor listened to his complaints, announced, “You’re depressed,” and handed
him a prescription for an antidepressant.
But Jeff was smart enough to know that his depression was not the cause of his fatigue. It was
the other way around. He was even aware that caffeine was part of the problem, but he didn’t think
there was any alternative. Everyone at work was a caffeine addict. It was part of the culture.
The first thing I did with Jeff was to create an agreement. If he would follow my Off the Bean
program step by step without fail, I would guarantee that in sixty days, he’d feel better and have
more energy. It was a no-lose proposition for Jeff. After all, if I was wrong, he could always go back
to the coffee. We measured his blood pressure, heart rate, and weight. He filled out a questionnaire
like the one in Appendix C, and we took a photograph. That kind of documentation is extremely
valuable in charting one’s progress.
I have no doubt that if I had simply told Jeff to cut out coffee, he would have left my office and
never come back. But the program made sense to him, and in just two weeks, he was able to reduce
his caffeine intake by 50 percent with no headache or fatigue. He called a few days later to tell me
that for the first time in years, he had awakened before the alarm clock went off. By the end of the
month, he was down to one cup of coffee in the morning and a cup of tea in the afternoon.
During the next thirty days, Jeff experienced remarkable improvements in his energy level.
Before, his days had been like a roller coaster, with peaks of creativity and alertness alternating with
mental fog and profound fatigue. Now he was sailing through the day with consistent energy and
clarity. Even the dreaded three-o’clock slump had disappeared. His appearance had improved and
he’d lost weight, but the most important benefit for him was his attitude. Jeff felt like himself again:
optimistic, energetic—and happy!
Now the Hollywood ending would be Jeff becoming a partner in the firm, but that’s not what
happened. The experience of near burnout convinced Jeff that the price of success in that arena was
much too high. So he took his renewed energy and went to work for a smaller company. At his new
job, he didn’t have to watch his back constantly, so he was able to spend more time in creative
pursuits. A year later, he was doing quite well and enjoying life immensely, along with a few cups
of caffeine-free herbal tea every day.
Critical Point #11: Malnutrition
Malnutrition is one of the most well-defined effects of habitual caffeine intake. It contributes in a
very logical way to a host of disorders that we will explore in Chapter 5. Caffeine, and possibly
other ingredients in coffee and tea, causes an increased loss of thiamin and other B vitamins in the
urine.43–44, 45 There is evidence that caffeic acid also decreases the bioavailability of thiamin so that
less of this vital nutrient is absorbed from food46. Since the B vitamin status of many Americans is
borderline to begin with, regular consumption of coffee and soft drinks can contribute to deficiency
and a raft of symptoms, including neurological damage.47
Then there is the loss of calcium and other minerals. Researchers at Washington State
University’s Department of Food Science and Human Nutrition found that as little as 150
milligrams of caffeine caused increased loss of calcium, magnesium, sodium, and chloride in the
urine.48 The losses were far greater when the caffeine intake was raised to 300 milligrams. Research
just published in the Annals of Nutrition and Metabolism found that caffeine increased potassium
loss by nearly one-third.49 To make matters worse, such mineral loss appears to be accelerated when
caffeine is mixed with sugar.50 Studies show that the mechanism behind this mineral-wasting
phenomenon may have to do with the fact that caffeine impairs the kidneys’ ability to hold on to
calcium, magnesium, and other minerals.51 Most recently, zinc was added to the list of nutrients
depleted by caffeine.52
As you read this, you might be wondering how caffeine affects your bones. In fact, all that
calcium loss cannot help but increase your risk for osteoporosis, and perhaps hypertension as well.
As you will see in Chapters 6 and 8, caffeinated soft drinks create special problems for women. The
caffeine causes increased urinary loss of calcium, while another ingredient, phosphoric acid,
interferes with the absorption and metabolism of that important mineral. The result? Studies have
shown that high caffeinated soft drink consumption is associated with increased fracture risk among
women53 and girls.54
ANEMIA ANYONE?
Perhaps an even greater nutritional problem has to do with the effect of caffeine on iron absorption.
In the late 1970s, researchers stumbled upon an important discovery. Nutritionists were looking for
ways to increase iron intake and came up with the idea of fortifying sugar with the mineral. (No
comment!) However, they found that when iron-fortified sugar was added to coffee, very little iron
was absorbed. This prompted further investigation, and in 1981, the American Journal of ’clinical
Nutrition reported research showing that caffeine may oxidize available iron, converting it to a form
with dramatically reduced bio-availability.55
Other studies showed that a single cup of coffee can reduce iron absorption from a meal by as
much as 75 percent. What’s more, this dramatic inhibition of iron absorption occurred even when
the coffee was consumed an hour after a meal. And if you think you can compensate for this
handicap by taking vitamins or minerals, you’re wrong. Coffee and tea both reduce the effectiveness
of iron supplements.56,57
The salient point here is that over 30 percent of American women spend their entire lives with
suboptimal iron status. In many cases, that leads to iron deficiency and a disorder known as anemia
(deficiency in the blood’s oxygen-carrying ability), but low iron can seriously affect energy,
immunity, and even brain function long before anemia develops (see Chapter 6).
Critical Point #12: Caffeine and Immunity
We have already explored the disastrous effects that excess stress hormones have on immunity
(Critical Point #7). But caffeine and other methylxanthines may also exert negative pressure directly
on your body’s defense system by reducing the activity of monocytes and natural killer (NK)
cells.58–59, 60, 61When you understand that these immune cells are your best protection against
viruses and cancer, you ; begin to see the seriousness of the problem.
Now here’s some good news. Recent research has shown that the number and immune strength
of monocytes and NK cells can be enhanced by the administration of DHEA.62,63 Remember,
however, that excess stress hormones will decrease and/or deplete your body’s own production of
DHEA so that in order to benefit from DHEA, reduction of caffeine intake is imperative.
CAFFEINE VERSUS MELATONIN
Melatonin is another vital hormone, and it’s an extremely hot topic in immunology these days. For
decades melatonin was thought simply to regulate the sleep/wake cycle in humans and animals.
Now research is showing that it has powerful and important immune functions, including anti-
cancer activity and the antioxidant ability to “scavenge” dangerous molecules known as free
radicals. You’ve probably heard a great deal about other antioxidants, such as vitamin C and vitamin
E, but melatonin’s role is only now coming to light. One group of researchers, after presenting
stunning evidence of melatonin’s ability to protect cellular DNA, concluded that this hormone “may
prove to be the most important free radical scavenger discovered to date.”64
Like DHEA, production of melatonin decreases with advancing years. Again, this was first
thought to be one of those inevitable consequences of aging, but if you are smart, you’ll start to
question anything that is said to be inevitable. And when you look for the reason why melatonin
levels fall with age, you come fact-to-face with a familiar duo: caffeine and stress.
You’ll remember that stress leads to decreased DHEA through a kind of metabolic
“competition.” The adrenals just can’t produce large amount of both DHEA and stress hormones.
But melatonin in produced by the pineal gland in the brain as well as other cells in the intestinal
tract, so the mechanism by which stress lowers melatonin is not fully understood.
We get a clue, however, from recent research showing that melatonin (in addition to its sleep
and immune system duties) is also an anti-anxiety agent.65 It may be that stress simply “use up” or
depletes this vitally important hormone. We also know that cortisol radically disrupts the normal
secretion of melatonin,66 and that stress and coffee (even decaf) can damage cells of the intestinal
tract that secrete the hormone.67
The most recent (and most damning) piece of evidence illustrates that caffeine directly
suppresses melatonin production. Researchers have long known that exposure to bright light
decreases melatonin, while dim lighting promotes secretion of the hormone. A new study in the
journal Brain Research showed that when normal human subjects were given caffeine or placebo,
caffeine resulted in significantly lower levels of melatonin, even when lighting conditions were dim.
As expected, bright light conditions lowered melatonin as well, but the combination of bright light
and caffeine produced a striking decrease, far more than would result from either condition alone. In
other words, bright light and caffeine had an additive effect in depressing the subjects’ production of
melatonin.68
Thus, whether through depletion or through impaired production, stress, anxiety, and caffeine
combine to reduce the amount of melatonin available to our bodies. And that, according to leading
experts, is a metabolic catastrophe that leads to crippled immunity, impaired sleep, and accelerated
aging.69,70
Imagine you lived in a country that was always under threat of attack. No matter where you went,
there was a perpetual state of alert. Not only that, but your defenses were constantly being depleted
and weakened. Does that sound stressful? Caffeine produces the same effect on your body, like
fighting a war on multiple fronts at the same time. All organ systems are strained during times of
stress, but most important are the adrenals, which must supply hormones to activate the body’s
emergency functions.
Remember, however, that the caffeine “emergency” is not a real threat to survival. While the
adrenals are busy fighting a phantom enemy, real enemies may go unchecked. The adrenals are
responsible for helping mount an immune attack against a wide range of pathogens. Studies show
that adrenal hormone production may triple during acute infection71 If stress is prolonged, adaptive
mechanisms may fail, leading to serious and chronic illness.72
Let’s face it, remaining healthy and strong throughout life is a battle. Caffeine is the Trojan
horse. It looks like a gift but instead delivers adrenal stress, low blood sugar, mood and energy
swings, fatigue, depression, malnutrition, and disturbed sleep. By now, you are starting to see the
full scope of how caffeine affects the quality of life. In Chapter 5 we’re going to see how these
twelve critical points contribute to specific disease states. I want to emphasize again how insidious
this downward spiral is. Caffeinism is a gradual and at first imperceptible disorder. And because all
your friends are also getting tired and becoming sick more often, it’s natural to assume that these
signs and symptoms are inevitable.
Of course, some of the effects are obvious. You can measure increases in blood pressure, and
you can feel the coldness resulting from constriction of blood vessels in your fingers. But most of
the stress is very subtle. There is no way to measure irritability, for example. People who have never
known you off coffee just assume that is your personality.
Another gradual effect of caffeinism is that your concentration becomes one-dimensional. You
tend to lose the big picture because you can’t step back from what you’re involved in. Coffee
concentration is good for some tasks but terribly limiting when, for example, you have to deal with
any kind of adversity or setback. Coffee cuts you off from the brain’s higher centers of reason and
evaluation because you are forcing your brain into defensive, emergency overdrive.
In yet another ironic example of wrong thinking, we often view such limitations as advantages.
We talk about a “competitive edge” as if success depended only upon aggressiveness. In reality, this
type of success often comes at the price of burnout and ruined health, and I have seen it scores of
times in my clinical practice and in the first-class cabin of 747s.
I travel a great deal, and very often find myself sitting next to successful businesspeople. It is
amazing to me how often they will maintain a frenzied work pace throughout the flight, tapping
away at their laptops, talking on the phone, faxing letters. And all the while, the flight attendant
keeps their coffee cups filled.
During a meal, when there’s a lull in the action, it’s natural to strike up a conversation and, as
you can imagine, it often centers around what we do for a living. More times than not, the man or
woman is in a high-pressure executive position. They’re usually heavy coffee drinkers and almost
always have significant health problems directly related to stress. I’m a good listener, and I often
feel like a therapist as my neighbor describes his or her physical and emotional pain. In short, the
vast majority of these successful people feel like they’re trapped on a treadmill.
But there are the exceptions, people who live with no frenzy or turmoil. These people are
generally healthier, more fit, and definitely happier than the treadmill crowd. And the most
significant difference is not their income but their attitude. They tend to drink less (or no) caffeine,
and they understand that true success is a balance. I have heard remarkable wisdom from these
people, about how their lives changed when they realized that business does not have to be self-
destructive. I’ve talked with award-winning salespeople who experienced dramatic gains after
getting off caffeine. Many have described a completely different approach that opened doors that
before had been slammed in their faces. What made the difference? One man told me, “I was less
aggressive but far more effective. I was able to relate to the customer’s needs more clearly, and once
they realized that I was not trying to steamroll them, they were more open to what I had to say.”
With sales, as in life, we make decisions every day that affect how we feel. The lessons for me
has been clear, because I am convinced that what we get out of life depends on the kind of energy
we put into it. The caffeine-driven go-getter may accomplish a great deal at first, but suffering is
sure to follow. With the tools presented in this book, I believe that we now have a much more
rewarding alternative.
CHAPTER 4
Caffeine and Your Mind
If you ask people what caffeine does for them, most will tell you that it sharpens their minds.
However, this perception is only true in the sense that stress increases alertness. We know, for
example, that we tend to remember traumatic events very clearly. Everyone remembers what they
were doing the day Kennedy was shot. Eons ago, this survival mechanism helped us to remember
(and thereby avoid) dangerous situations when such an ability meant the difference between life and
death.
But today, millions of people create artificial stress by ingesting caffeine numerous times every
day, and then they marvel at the way it “sharpens” their minds. In this chapter, we’ll look at the
mental and emotional downside of caffeine, what happens to your brain and nervous system when
they are subjected to this constant stress. We’ll look at three different aspects of caffeine: the
physiological effects; how those affects alter mind, mood, and behavior; and finally the emotional
consequences, including anxiety, depression, and other psychological disorders.
Studies show conclusively that caffeine contributes to anxiety, irritability, panic attacks,
depression, and anger. With high levels of caffeine in your blood, even the small annoyances of life
can gain tragic proportions. The irony of it all, of course, is that when people are feeling stressed,
they tend to drink more coffee. On the surface, that appears to make sense because much of the time
we feel the need for a little more energy. But what you get from caffeine is really not energy; it’s
metabolic and neurologic stress.
Another part of the coffee illusion is created by advertisers who tell us that coffee is what you
drink when you have to sort things out. Nothing could be farther from the truth. Even the term
coffee break is absurd, as the net result of ingesting coffee is merely greater stress and decreased
ability to cope.
Nuts and Bolts: Caffeine and Brain Function
In Chapter 3, we discussed how caffeine interferes with the normal control of neuron firing in the
brain. Caffeine triggers a stress response that involves a surge in adrenal hormones and the classic
fight-or-fiight “emergency,” affecting virtually every cell in the body.1
This stress response has an undeniable impact on the nervous system. We know that people
living under threat of attack suffer greatly from the stress, even if the attack never comes. Likewise,
caffeine creates background tension that ultimately reduces the quality of life, an effect that may go
unnoticed because it is masked by other stressors.
However, unlike many other vicissitudes of life, we can do something about the levels of
caffeine we consume. At some point, most people realize that peace of mind is a highly desirable
experience. And the time to do something about your caffeine intake is before that peace is
shattered.
The Stress/Distress Threshold
In Chapter 3,1 presented the concept of a threshold point at which stress becomes damaging to the
body This is also true for the mind, and the undeniable fact is that caffeine lowers that threshold
point by creating anxiety, irritability, anger, and hostility. In other words, events that we would
normally cope with successfully send us flying off the handle. Our responses can take many forms,
from outward expressions of frustration to silent rage.
Emotional Resilience
Life is complex and unpredictable, and to negotiate its challenges requires flexibility, understanding,
and a sense of harmony and inner balance. The previous illustration at the left represents what could
be called emotional resilience: the ability to “roll with the punches,” to cope successfully and
maintain a sense of peace in one’s life.
For people amped out on caffeine, however, the margin of emotional health is very small. When
the first life stress comes along—be it illness, financial woes, public speaking, final exams,
relationship problems, or just getting a parking ticket—the experience destroys their peace of mind
and overwhelms them.
Caffeine promoters deny this problem, but their data is artificial if not purposely misleading. For
example, in research designed to evaluate the effect of caffeine on behavior, people who are under
significant stress are usually removed from the study group, presumably because they would exhibit
an “overreaction” to caffeine. Does this make sense?
A more accurate and meaningful line of inquiry would include such people because they are the
most likely to be harmed. The best approach would be to evaluate the cumulative effect of stress
resulting from both environmental and caffeine sources. One landmark study measured the effect of
caffeine on military recruits and found that caffeine was a significant contributing factor to the
development of combat-stress syndrome. The researchers concluded that “the use of decaffeinated
coffee in military settings might reduce the prevalence of the various anxiety reactions, including
combat-stress reaction.”2
Such research fits perfectly into the model of emotional resilience and points toward a better
understanding of the role of caffeine in health and disease. Now follow this line of reasoning to the
next step, which is to acknowledge that emotional health and physical health are absolutely
inseparable. Every day, more and more research is published in support of the body-mind
connection, including studies that show stress to be not just a contributing factor, but a major factor
in a wide range of health disorders. Thus, the model of emotional resilience can be expanded to
include physical as well as emotional health.
“Stress plays a significant role in more than half of the complaints that bring
patients to the physicians office.”
Source: The Physician and Sportsmedicine, 1994;22(7):66.
The role of stress is perfectly illustrated by a report in the Journal of the American Medical
Association showing that stress can alter brain biochemistry in such a way that the effects of
subsequent events are greatly magnified. Animals exposed to stress, for example, will exhibit
heightened aggressiveness long after the stressful event is over. And it’s not just for a few hours.
Abnormal brain chemistry and 200 percent increases in aggressive behavior have been observed for
up to a month.3 In other words, stress can produce long-lasting alterations in neu-rotransmitter
production in the brain, resulting in higher levels of norepinephrine and a subsequent increase in
anxiety and hostility. The take-home message here is that there is a cumulative effect of stress in our
lives, and caffeine is an important part of the increasing harm that we experience.
ROBERTA BREAKS THE CYCLE
Roberta was a light coffee drinker and worked in a moderately stressful job as an administrative
assistant. When her boss was promoted to CEO, the demands on her were greatly increased.
Suddenly, she found herself working overtime, coming in early, and traveling three or four times a
month. What’s more, the intensity level of every day was increased because of her new
responsibilities. She faced the challenge with determination—and caffeine. Soon, she was drinking
coffee before she left the house, another cup as soon as she arrived at the office, a cup at
midmorning, and a soft drink with lunch. Then there was tea or another soft drink in the afternoon.
The increased work hours started to cause problems at home. She was late picking up her son at
child care more often than she was on time, and family demands only added to her stress. When
Roberta came to see me, she was near the breaking point. She was experiencing headaches and
muscle pain, and she hadn’t exercised in months.
“All I need is a rest,” she said. “Can you help me get through these next few months till my
vacation?” I explained that I didn’t agree with her line of thinking, and pointed out that unless she
handled the underlying stress, she would be in the same plight a few weeks after her vacation. She
insisted that a vacation would fix everything, so I drew the following diagram to make my point. I
call it “the vacation illusion.”
Roberta thought that she could push herself to the breaking point and that periodic vacations
would prevent her from experiencing stress-induced disease and breakdown. Stress, however, has a
cumulative effect, and this is compounded by caffeine. What she didn’t take into consideration was
that the damage being done to her nervous system would make her less and less able to cope with
her job. For Roberta and millions of others, the vacation reality actually looks like this:
Note the upward slope of the stress curve. Each vacation provides less relaxation and
rejuvenation, followed by greater stress, building to ultimate burnout. The question Robert asked, of
course, was how to get off this upward spiral without quitting her job. And my answer was “Get off
caffeine and give yourself a thirty-minute stress-management break every day.”
Now you’re probably thinking that without caffeine, you couldn’t accomplish everything that
needs to be done, so I will give you the same suggestion I gave Roberta: Follow my Off the Bean
program, which includes a nutritional plan to enhance energy and mental acuity, and see how it
makes life easier and more enjoyable. My program worked splendidly for Roberta. She was not only
better able to cope with the various tasks of her job, but she found that she was working more
efficiently with co-workers and spending less time “spinning her wheels.” As she told me, “When I
was running on caffeine, I thought I was doing a bang-up job, but I was really just banging around.”
Don’t Be Happy—Be Worried
To review, caffeine interferes with adenosine receptors, which normally control the rate of neuron
firing in the brain. In addition, the drug interferes with the metabolism of GABA, an important
biochemical that helps us filter information and plan sensible action strategies.4 So the caffeine-
stress combination, in effect, turns up the activity level in your brain while at the same time
lowering your coping skills and decreasing your ability to relax. The result? Anxiety and irritability.
The amazing thing is that even without knowing how this occurs, most people know that
caffeine makes them nervous. Yet a common reaction is not to decrease intake of caffeine, but to
reach for anti-anxiety drugs. Today, one out of every five American adults takes some form of tran-
quilizer or antidepressant. Since seven out of every ten American adults drink coffee, it’s safe to
assume that many individuals drink coffee and take tranquilizers. This behavior is equivalent to
driving with one foot on the brake and one foot on the gas. No wonder so many people are falling
apart.
Truth in Advertising
An ad recently ran in national magazines that asked, “Does your life have signs of persistent
anxiety?” It went on to list symptoms such as sleep disturbance, irritability, muscle tension,
restlessness, and fatigue. Is this a “quit coffee” ad? No, this was an advertisement for Buspar, a new
anti-anxiety drug from Bristol-Myers Squibb. Nowhere did the ad mention that every one of these
symptoms could result from the consumption of caffeine. Nor did the prescribing information (in the
Physicians’ Desk Reference) recommend that doctors query their patients regarding their caffeine
intake before prescribing the drug.
Beyond Anxiety: Panic Disorder
For an estimated 5 million Americans, anxiety progresses to a condition known as panic disorder.5
The onset of panic “attacks” usually occurs in the third decade of life, and it afflicts women three
times more often than men. Panic disorder is characterized by unexpected, unprovoked and intense
fear, usually including feelings of impending doom. The accompanying symptoms of rapid
heartbeat, shortness of breath, palpitation, dizziness, sweating, and a feeling of helplessness make
this condition truly and deeply frightening. A panic attack may last only minutes, or it,, may last
hours.
Now I’m not saying that panic attacks are caused by caffeine, but look back at the model of
emotional resilience and imagine a paper-thin margin of emotional health. Think of the possible
triggers that could send someone’s nervous system into a tailspin. One of the most significant is
caffeine.
CHECKLIST #1: ANXIETY/PANIC DISORDER
Medical and scientific analysis of anxiety/panic disorder has revealed well-defined abnormalities in
physiology and brain biochemistry in people who suffer from the condition.6–7, 8, 9, 10 These
include:
1. Overproduction of adrenal stress hormones, including increased norepinephrine and
cortisol.
Is caffeine a factor? Yes_
2. Increased incidence of mitral valve prolapse (MVP).
Is caffeine a factor? Yes_
3. Decreased nighttime melatonin production.
Is caffeine a factor? Yes_
4. Dysfunction of GABA metabolism.
Is caffeine a factor? Yes_
5. Increased neuron firing in the brain.
Is caffeine a factor? Yes_
6. Decreased blood circulation to the brain.
Is caffeine a factor? Yes_
What’s more, in someone prone to this disorder, caffeine ingestion can trigger panic attacks.11 Still,
caffeine promoters dismiss this characterization of their product, claiming that if caffeine were so
bad, nearly everyone would have an anxiety disorder. That response is reminiscent of the cigarette
makers who (until recently) defended their product by stating, “If cigarettes are so bad, every
smoker would get cancer.” Of course not every smoker gets cancer and not every caffeine user has
panic attacks. But it is important to understand that there is a continuum of effects. Everyone who
smokes is destroying lung tissue, and in many cases that will progress to cancer. Likewise, everyone
who abuses caffeine is harming his or her nervous system, and in many cases, that will progress to
anxiety and perhaps panic attacks.
A Look at the Literature
Evidence of a connection between caffeine and anxiety/panic disorder is well established in the
medical literature. Back in 1936, the New England Journal of Medicine reported that a woman
became “confused, disoriented, excited, restless and violent” after ingesting a large number of
caffeine pills. She was brought to the hospital, where the staff, ignorant of her caffeine binge, made
the diagnosis of “psychoneurosis, anxiety type, with a hysterical episode.”
Five weeks later, the same woman again took over 1,000 milligrams of caffeine tablets, and was
returned to the hospital. When she did not improve, she was transferred to a psychiatric hospital,
where she was strapped to her bed. After two months during which she made a slow recovery, she
suddenly took a turn for the worse. Finally, someone noticed that she was drinking four cups of
coffee per day. When the coffee was withdrawn, “she became entirely normal and was dismissed
froni the hospital.”12
A more recent study published in the, Journal of Clinical Psychiatry reported that caffeine is not
only capable of triggering panic attacks, but can also increase their frequency and intensity.13 Even
moderate intake of caffeine has been found to worsen anxiety,14 and in a typical vicious cycle,
individuals with anxiety and depression have been found to exhibit increased sensitivity to
caffeine.15, 16 Finally, a report in the Archives of General Psychiatry found that caffeine produced
significant increases in anxiety, nervousness, fear, nausea, palpitations, restlessness, and tremors in
patients with agoraphobia and panic disorders. In fact, 71 percent of the patients reported that the
behavioral effects of caffeine were similar to those experienced during panic attacks.17
Is the caffeine connection widely unrecognized? Surveys document that 70 percent of patients
with panic disorder visited physicians ten or more times before they experienced relief of their
symptoms.18 The fact is that few physicians conduct a careful evaluation of caffeine intake, even
though the medical literature is conclusive on the benefits of caffeine reduction in virtually all
anxiety disorders.
Where Are You on the Caffeine/Anxiety Scale?
Emotional health is not an all-or-nothing state. There is a continuum of feelings and experiences that
range all the way from deep serenity to panic. Where would you place yourself on this scale, and
where would you like to be?
A clinical report published in the Journal of Affective Disorders graphically illustrates the
connection between caffeine and depression. A woman suffered for twenty years with recurrent
depression. She was treated with a variety of drugs, including lithium, chlorpromazine, haloperidol,
and Valium. After years of drug therapy, she decided to quit drinking coffee. Within one month, she
was able to eliminate the Valium and all but one of her medications. At the time the clinical report
was published, she had gone five years without a single episode of depression.30
Another Vicious Cycle
Depression can also occur as an adverse side effect of certain medications, and once again, caffeine
is often a factor. Consider the example of a fifty-year-old man with high blood pressure who is put
on a popular class of drugs called beta-blockers (e.g., propranolol). Depression and fatigue are
common side effects with these drugs.31 Now the fellow is also drinking coffee, which contributes
to his hypertension, and, faced with depression and fatigue, he then drinks even more coffee to
break out of the depressed state. Thus, his blood pressure stays elevated and his doctor responds by
increasing the medication dose, which causes the man to become more depressed.
A Word about Antidepressants
The pharmaceutical industry continues to spend billions to develop and market antidepressant
drugs. Three main categories, including tricyclic antidepressants (TCAs), MAO inhibitors, and the
new class of selective serotonin reuptake inhibitors (SSRIs) can all be very valuable, and all can
have significant side effects. Of the three classes, MAO inhibitors have the longest list of serious
side effects, mostly having to do with increased risk of heart disease. Common side effects include
headache, dizziness, and insomnia. TCAs also have significant cardiovascular risks (elevated blood
pressure, rapid heartbeat, palpitation, arrhythmias), and the new SSRIs, while having numerically
fewer side effects, have as their primary disadvantage frequent reports of anxiety, insomnia,
nervousness, and tremor.32, 33 Believe it or not, with these common adverse side effects, none of
these drugs list coffee as a beverage to avoid in their professional or patient literature.
CHECKLIST #2: DEPRESSION
Mental health professionals have observed that depression is often the other side of anxiety.34, 35 In
other words, a drug (like caffeine) that creates anxiety will ultimately contribute to depression.
Depression is characterized by well-defined biochemical and behavioral abnormalities, all of which
are aggravated by caffeine.36–37, 38, 39, 40 They include:
1. Overproduction of stress hormones, including increased ACTH and cortisol.
Is caffeine a factor? Yes_
2. Strong association with insomnia and sleep disturbance.
Is caffeine a factor? Yes_
3. Decreased nighttime melatonin production.
Is caffeine a factor? Yes_
4. Dysfunction of GABA metabolism.
Is caffeine a factor? Yes_
5. Alteration of serotonin levels in the brain.
Is caffeine a factor? Yes_
6. Strong association with life stress.
Is caffeine a factor? Yes_
But I’m Not Depressed!
If you’re a coffee drinker, you may be thinking, “Well, I drink coffee and I’m not depressed.” It’s
necessary to state again that everyone is different, and also that depression can be quite subtle.
Throughout this book, I am suggesting that you will never know the full effect the drug is having on
you until you experience what life is like caffeine free. Over the years, I have heard similar
responses from hundreds of clients: “Wow, I never realized that caffeine made me so [select one:
anxious, depressed, irritable].”
In addition, research shows that there are a number of variables affecting the depressive side of
caffeine. A recent study measuring the stress hormone cortisol (raised by caffeine consumption) is
revealing. Researchers found that in collegiate swimmers, there was a powerful correlation between
cortisol levels and depression, but only during periods of intense training.41 Thus, there appears to
be a cumulative stress phenomenon, which may be present at certain times and absent at other times.
Having this information and being sensitive to your moods will enable you to take the appropriate
steps should you start to notice periods of depression.
Above all, I want you to avoid the common mistake of reaching for the coffeepot when you’re
feeling “blue.” Coffee may help temporarily, but clinical and laboratory evidence suggests strongly
that you will pay a steep price later on. Ironically, the group most likely to use caffeine in an attempt
to change their state of mind are those suffering from clinical depression.42
DAVE KICKS CAFFEINE, SLEEPS BETTER, FEELS BRIGHTER
Dave was a typical, hardworking middle-management professional. And like so many, his intake of
caffeine had slowly escalated to four cups a day, the last one coming around 3 P.M. to get him
through the overtime hours. Always looking for the competitive edge, he read an article in a health
magazine that recommended eight hours of sleep for peak mental performance. That was when he
realized that he suffered from insomnia. He was having a hard time getting to sleep, and would often
read in bed or watch TV until 1 A.M.
His doctor gave him Ambien, a sleep medication, and told Dave to cut back on coffee. So he
dropped the 3 P.M. cup. He started falling asleep earlier, but then he noticed that he was getting “the
blahs” almost every afternoon. Not realizing that it was related to caffeine withdrawal, Dave blamed
his depression on the sleeping pills. When he came to my office, he said he was looking for a
“natural sleeping pill that wouldn’t make him depressed,” but it didn’t take me long to see the real
problem.
“You don’t have insomnia because of an Ambien deficiency,” I told him. “Ambien may help,
but I believe you will do much better by getting off caffeine altogether. Caffeine is keeping you
awake at night and caffeine is making you depressed.” Dave didn’t like this suggestion, even though
I assured him that he would have more energy, a better attitude, and a sharper mind with my Off the
Bean program (see Chapter 10). Instead he went back to his doctor, who gave him a prescription for
a popular antidepressant.
After a month on the two drugs, Dave felt worse than ever. He was falling asleep all right, but
he awoke feeling tired. He felt that his motivation, the sharpness he needed in his competitive field,
was gone. He wasn’t depressed, but he also wasn’t feeling great. By the time he got back to me,
he’d stopped exercising, and he knew that was not a good sign.
“Look,” I told him, repeating a rationale I had used a thousand times before. “If you try my
program and don’t feel a great deal better, you can always go back to your caffeine, sleeping pills,
and antidepressants.” So Dave agreed to give it a try, and over a period of three weeks, he got off
coffee entirely. Shortly after that, he was able to discontinue both medications, and that’s when his
life really improved.
“At the end of a month,” said Dave, “it was as if the sun broke through. I felt optimistic and
powerful. And I was keenly aware that the energy and enthusiasm I was experiencing was coming
from me, not a coffee mug. I got back into exercising, performed better at my job, and now look
back on my caffeine addiction like a junkie who’s finally kicked the habit.”
Depression and Sleep
Dave’s case illustrates another facet of the caffeine-depression connection. Sleep is disturbed in 90
percent of patients with depression. The conventional belief is that when people are depressed, they
naturally have difficulty sleeping. New research, however, shows that this is not the case. A study
published in the Journal of Clinical Psychiatry found that curing the depression does not necessarily
eliminate the sleep problem.43 The most likely explanation? Depressed individuals frequently use
caffeine to give themselves a “lift.” This habit perpetuates their sleep disorders and greatly increases
the likelihood of recurrent depression.
What’s more, sleep disturbance is a common side effect of antidepressant medications. New
studies presented in Europe indicate that selective serotonin reuptake inhibitors (SSRIs)—which
include the popular antidepressant Prozac—can seriously interrupt sleep patterns, making people
feel drowsy during the day.44
The vicious cycle could not be more clear. Caffeine contributes to depression, but, not knowing
this, people take antidepressant drugs. Both the drugs and the caffeine dis turb their sleep, causing
them to feel tired during the day, which causes them to drink more coffee. The only way to break
this cycle is to get offthe caffeine. Then you will be able to discern whether or not you truly need an
antidepressant.
Depression or Fatigue: Which Comes First?
Fatigue is one of the most frequent reasons why Americans seek medical help.45 It is also one of the
most obvious causes of depression, and a source of some confusion among medical professionals.
Mrs. Jones turns to her doctor for help with her fatigue and, after ruling out anemia and other
disease factors, the doctor will often announce that she is “simply” depressed.
I find this response to be insensitive and unscientific. After all, it is entirely possible that the
doctor was simply unable to find the cause of fatigue, and saying that she is depressed, while
technically accurate, misses the point. In reality, anyone who becomes fatigued will ultimately
become depressed.
The converse is also true. Depressed individuals will invariably experience fatigue. In fact, not
all depressed people feel sad. Many just feel bone-weary. So we have another vicious cycle that
requires a search for root causes, not a quick diagnosis and a prescription for antidepres-sants. The
caffeine-depression connection is very clear, but caffeine’s contribution to fatigue is often difficult
to see. That’s because we are so used to thinking of caffeine as an energizing substance.
It might be good to review the stress-fatigue cycle described in Chapter 3, remembering that
caffeine does not provide energy at all, but only delivers a temporary shock to the nervous system
that feels like a boost. Think of an exhausted fighter in his corner and the trainer slapping him in the
face to get him ready for the next round.
The truth about caffeine and energy is finally getting out. Physicians are starting to warn their
patients about caffeine “rebound,” and an article in U.S. News & World Report listed caffeine
addiction as a major cause of fatigue, including a “crash” that occurs after caffeine “buzz” wears
off.46 People who become aware of this powerful influence on energy and mood and take steps to
improve their energy naturally (see Chapter 10) can experience remarkable improvements in their
quality of life.
Mental and Emotional Effects of Caffeine
• Chronic caffeine ingestion may cause or exacerbate anxiety and may be associated with
depression and increased use of anti-anxiety drugs.
• Caffeine may cause anxiety and panic in panic disorder patients.
• Caffeine may aggravate the symptoms of premenstrual syndrome.
• Chronic users who are caffeine-sensitive may have symptoms of caffeinism at relatively
low doses.
• Individual who regularly consume moderate to heavy amounts of caffeine may develop
caffeinism, or they may show signs of caffeine withdrawal syndrome after abstaining from
the drug.
Source: G. L. Clementz and J. W! Dailey, “Psychotropic Effects of Caffeine,”
American Family Physician, May 1988;37(5): 167–72.
Is Coffee the “Think Drink”? Think Again!
Students the world over use caffeine not only to stay awake, but also because they believe the drug
will improve their performance on exams. Solid research, however, - illustrates that as little as 100
milligrams of caffeine (a six-ounce serving) can cause a significant decrease in recall and reasoning.
One study compared scores on a memory test called the Auditory-Verbal Learning Test, or
AVLT. College students who were given 100 milligrams of caffeine recalled significantly fewer
words than those given a placebo beverage. These results were found in both single and multiple
presentation trials. Interestingly, subjects given caffeine did fine at the beginning of the test, but
were particularly weak in the middle to end portions of the study.47 This illustrates that the
“enhancement” of alertness provided by caffeine is both temporary and illusory.
Research has also found that caffeine ingestion is associated with lower academic performance
and greater incidence of psychosomatic illness.48 Ironically, when students are given a questionnaire
to evaluate their expectation of benefits from caffeine, those with the highest expectations turn out
to be those who consume the most caffeine and who experience greater levels of anxiety,
depression, insomnia, headache, and fatigue.49 I believe that heavy caffeine consumption is a
significant factor in the epidemic of anxiety suffered by college students. One recent study found
that 34 percent of students surveyed were experiencing anxiety sufficient to cause clinical symptoms
of psychosomatic illness.50
Caffeine Boggles the Brain
How does caffeine decrease mental acuity and cause all these problems? There are a number of
possible explanations, the first of course being stress. Nature did not design the stress response to
enable us to engage in abstract or global reasoning, such as may be required for complex tasks or
final exams. The stress response causes a shift of mental function to a very primitive survival-
oriented part of the brain known as the limbic system.51 Once again, this is great if you’re engaged
in a fight-or-flight situation, but not so great if you’re trying to write an essay on the fall of the
Roman Empire.
What’s more, adenosine receptor antagonists (such as caffeine) have a depressive effect on other
brain biochem-icals, such as acetylcholine.52, 53 Since acetylcholine is a neurotransmitter directly
involved in memory and learning, this could account for some of the observed negative effects. In
support of this theory, researchers generally have found that simple tasks such as assembly-line
work are enhanced by caffeine consumption, while complex reasoning skills are diminished.
Subjects asked to perform auditory recognition tasks, for example, where they had to process verbal
information, did worse after ingesting caffeine.54
Other eye-opening research has found that caffeine causes a remarkable decrease in cerebral
blood flow. You don’t have to be a neurochemist to see that such an effect would not be good for
memory, mood, and learning. Caffeine produces this effect, known as cerebral vasoconstric-tion, by
interfering with the normal relaxation of blood vessels in the brain.
“Caffeine, even in small doses, is a potent cerebral vasoconstrictor.”
Source: R. J. Matthew and W. H. Wilson, “Substance Abuse and Cerebral Blood
Flow,” American Journal of Psychiatry, March 1991;148(3):292-3O5.
Is the effect significant? One study illustrated that a dose of 250 milligrams (approximately
fifteen ounces of coffee) produced approximately a 30 percent decrease in whole-brain cerebral
blood flow.55 This is not only unfortunate, it’s dangerous, because at the same time, caffeine
increases blood pressure in the brain, leading to an increased risk for stroke.56 Researchers have also
found that caffeine reduces the oxygen level of brain tissues.57 With all of the attention on brain
health today (concerning depression, Alzheimer’s and Parkinson’s disease, as well as stroke) don’t
you think it’s a little odd that this data has not even made it to the evening news?
The Great Gaurana Hoax
Recently, manufacturers have been tripping over themselves to market products containing guarana,
a South American herb. Guarana (botanical name, Paulinia cupand) is in chewing gum, “energy”
drinks, a popular soft drink, and nutritional supplements purported to enhance sex drive, mental
acuity, and stamina. It’s hyped as an ancient Aztec secret, but the only secret is that guarana contains
more caffeine by weight than coffee beans. Manufacturers usually fail to mention that salient fact.
It’s also interesting to note that no manufacturer of guarana products has provided reliable
evidence of their effectiveness. In fact, studies have been performed that soundly debunk the
product claims. One group of researchers gave memory and learning tests to elderly volunteers.
Those given guarana performed no better than those given placebo.58 Another study found that
guarana actually had negative effects on a variety of learning tasks.59 The same is true for yerba
maté, another herbal source of caffeine.
The DHEA Connection, Part II
In Chapter 3, we learned that DHEA is a hormone that contributes to youthful energy, vitality, and
sex drive. Aside from the fact that it is converted by the body to testosterone and estrogen, DHEA
also plays an important role in memory, mood, and learning. Recent studies have found that
depressed individuals improve when DHEA levels are optimized, and this improvement includes
enhanced memory and feelings of well-being.60 But before you run to the health-food store to buy
DHEA, you must realize it’s not that simple. Stress and caffeine can abolish nearly all of the
neurological benefits you might obtain from DHEA.61
If you want the improvements in brain function that optimal levels of DHEA can provide, you’ll
have to cut back on caffeine. That’s because there is a tug-of-war going on in your body between
DHEA and stress hormones. When stress hormones predominate, your immune system, emotional
state, energy, vitality, and DHEA levels all suffer—and aging is accelerated as a result.
Can Caffeine Damage Your Brain?
Neurological damage from caffeine ingestion is far from proven, but consider the evidence. We
know that elderly individuals with symptoms of memory loss and disorien-tation have degeneration
of neurons in an area of the brain known as the hippocampus. In animal studies, raising stress
hormone levels produces neuron damage in that precise location.
What’s more, human studies support the concept of stress-induced hippocampal degeneration.
Using magnetic resonance imaging (MRI), researchers have found reduced hippocampal activity in
people under high stress conditions such as depression and post-traumatic stress disorder.
David Morgan of the University of South Florida’s Institute on Aging explains, “We think that
exposure to stress hormones, particularly high levels over a long period of time, may be responsible
for the minor learning deficits we have as we get older.”62 He goes on to assert that stress hormones
may be responsible for the chronic degenerative diseases that cause most deaths in older people. The
message is clear: Keeping levels of stress hormones as low as possible may determine to a great
extent the quality of life in your later years.
Caffeine and Mental Illness
If a person were injected with 500 milligrams of caffeine, within about an hour he or she would
exhibit symptoms of severe mental illness, among them, hallucinations, paranoia, panic, mania, and
depression. But the same amount of caffeine administered over the course of a day only pro duces
the milder forms of insanity for which we take tran-quilizers and antidepressants.
Mental and emotional health requires a sense of stability, and we have seen that caffeine creates
a roller-coaster effect throughout the nervous, endocrine, and cardiovascular systems. Thankfully,
mental health professionals are starting to take a close look at the caffeine connection. Regarding
the treatment of anxiety, recommendations are now being published to start with avoidance of
caffeine,63 and the latest edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM) includes an entire section on caffeinism.
However, research concerning caffeine and mental health is mixed, in great part because of the
way many studies are designed. In Chapter 1, I presented a study where hospitalized psychiatric
patients were switched to decaf coffee without their knowledge.64 When these individuals did not
improve, the conclusion was made that caffeine is not harmful to mental health. Given what we
know about the severe emotional and physical symptoms associated with caffeine withdrawal,
would anyone wonder why these people did not improve?
To evaluate the matter fairly, we need research that takes into account not only withdrawal, but
the fact that it can take three weeks or longer for stress hormones to return to normal after
discontinuing caffeine. In addition, it would be useful to know whether psychiatric patients consume
higher amounts of caffeine than the general population. One survey of psychiatric hospital
admissions found that patients consumed approximately five cups of coffee per day.65 Another put
the total even higher and noted that the heavy caffeine users were also most likely to suffer from
depression.66
In fact, a recent study revealed that about 40 percent of hospital inpatients consumed sufficient
caffeine to produce multiple symptoms of caffeinism—including anxiety, depression, and paranoid
delusion. Based upon these startling results, the authors recommend that all psychiatric patients be
questioned regarding their caffeine intake, and suggested that caffeinism should be viewed as a
primary contributing cause of anxiety-related emotional illness.67
Another facet of this important issue has to do with adverse reactions and long-term damage
that may be caused by caffeine s interaction with commonly prescribed psychiatric drugs.
Researchers are warning mental health professionals that caffeine can interfere with and even negate
the therapeutic benefits of these medications.68
Does any of this information surprise you? The fact is that caffeine has powerful neurological
effects, and it is unreasonable to expect that the drug would not cause harm to those whose nervous
systems are already shattered and stressed.
As if more evidence were required, two revealing studies have recently been conducted with
psychiatric patients. In the first, researchers gave schizophrenic patients a dose of caffeine
equivalent to about four cups of coffee. The caffeine raised blood levels of stress hormones and
produced significant behavior disturbances, as well as increased blood pressure.69 The second study
measured the effect of withdrawing caffeine from the diet of severely retarded adult patients. Two
weeks without caffeine produced no real improvement in sleep pattern or behavior, but
reintroduction of caffeine was accompanied by a highly significant increase in ward disturbance
ratings.70 These findings are consistent with the fact that it would take three weeks or longer for
caffeine-free patients to exhibit positive behavior changes.
“Our data suggest that inquiry into caffeine consumption should be included
routinely for psychiatric patients, e.g., at admission, because patients with a
psychotic disorder undergo a higher risk for an excessive caffeine consumption.”
Source: M. Rihs, C. Muller, and P. Baumann, “Caffeine Consumption in Hospitalized
Psychiatric Patients,” European Archives of Psychiatry and Clinical Neuroscience,
1996;246(2):83-92.
“[D]eleterious effects may result from the interaction of caffeine with commonly
prescribed psy-chotropic drugs. … Increased public education about potential
health problems related to caffeine consumption is suggested, and further controls
of caffeine in psychiatric settings are recommended.”
Source: A. Kruger, “Chronic Psychiatric Patients’ Use of Caffeine: Pharmacological
Effects and Mechanisms,” Psychology Reports, June 1996;78(3 Pt l):915-23.
Common Profiles of Caffeine Abusers
A great many people are addicted to caffine and abuse it without being aware of the consequences.
Depending on individual sensitivity, as little as two cups of coffee per day has been shown to
produce anxiety, insomnia, irritability, and dizziness.71
Dr. Michael Liepman, a clinician who works in addiction psychiatry at Michigan State
University/Kalamazoo Center for Medical Studies, has identified the following types of patients
who commonly abuse caffeine. Are you among them?
1. Patients with insomnia who are unaware that caffeine can disturb sleep for up to eight
hours. These individuals often obtain sleep medications (from physicians who do not take a
caffeine history) and then become doubly addicted, often escalating dosages of both drugs
over time.
2. Patients with anxiety disorder (panic disorder, generalized anxiety disorder [GAD])
whose symptoms are aggravated by caffeine.
3. Alcohol abusers who drink to counteract the anxiety and/or depression produced by
excess caffeine intake.
4. Recovering alcoholics who switch to caffeinated beverages once sober from alcohol.
They become anxious, experience an overwhelming craving for alcohol sedation, and then
relapse.
5. Hyperactive-appearing children who start on caffeinated beverages and chocolate (a
source of caffeine and theobromine). Such children often become wild and uncontrollable,
either ending up on stronger stimulants or sedating themselves with alcohol, marijuana, or
other drugs.
6. Patients on sedating drugs who increase their intake of caffeine to resist the sedation.
7. Patients who are taking drugs that include caffeine (e.g., painkillers) without knowing
that they contain caffeine.
8. Fetuses, newborn infants, and nursing infants whose mothers ingest caffeine from
multiple sources. The babies have disturbed sleep, which causes the mothers to become
sleep-deprived, whereupon the mothers increase their caffeine intake in order to function.
This last group is arguably the most serious because there are two “victims,” both of whom are
caught in a spiral of addiction and pain. We know, for example, that when pregnant women consume
caffeine, their babies are often born with a caffeine dependency. If these babies are bottle-fed, they
will experience withdrawal symptoms, and if you can imagine a newborn baby with insomnia and a
splitting headache, you understand the tragic consequences. Even if they are breast-fed, breast milk
does not contain as much caffeine as they were getting in the womb, and that may also trigger
withdrawal symptoms.
Then there’s the mother, who now has to deal with a child who cannot be consoled. Readers
who have raised fussy children will understand the strain that this creates. Multiply fussy times ten,
and you have the stress of a baby addicted to caffeine. As mentioned above, these mothers often turn
to caffeine to get through the day, and thus fall farther into the abyss of stress, disturbed sleep,
neurological damage, and emotional pain.
To Sleep, Perchance to Dream …
As described in Chapter 3, sleep is a critical factor in emotional and physical health. A perfectly
healthy and optimistic person will start to exhibit clear symptoms of emotional illness after only
three nights of disturbed sleep. In my clinical practice, I took a careful sleep inventory and found
that fewer than 25 percent of my patients had satisfactory sleep habits, in terms of duration,
consistency, and restfulness. The vast majority woke up feeling tired. And in most cases, significant
improvements were achieved simply by reducing or eliminating caffeine.
There is no mystery to this. Medical research conclusively shows that as stress hormones
increase, sleep duration and quality suffer greatly.72, 73 In many cases, this produces a well-defined
vicious cycle of caffeine intake -> anxiety -> depression -> impaired sleep -> increased caffeine
use.74
Reducing or eliminating caffeine is obviously the way to interrupt this cycle and restore a sense
of balance in one’s life. Invariably what surprised my patients was the profound difference they felt.
As sleep improves, you would expect an increase in energy, but the ripple effect of benefits also
included decreased pain, better mood, decreased reliance on prescription and over-the-counter
drugs, enhanced immune function, and improvements in memory and learning. Most important,
patients reported “feeling themselves” again. In some cases, where caffeine consumption had been
lifelong, they were literally discovering who they were for the first time.
Anger and Hostility
Getting off caffeine also tended to reduce feelings of irritability and hostility. This, of course, turns
out to be extremely valuable both from an individual and a social perspective. In the section on heart
disease (Chapter 5) I will present the connection between caffeine intake, stress hormones, and
behaviors like anger and hostility. You’ll learn that these behaviors are clearly linked to increased
risk for stroke and heart attack.75 Well, as you can imagine, cardiovascular disease is not the only
condition affected by anger and hostility. Mind-body research (known as psychoneuroimmunology)
tells us that the cycle of stress hormones and caffeine plays an important role in many if not most
health disorders, even traffic accidents.
According to the National Highway Traffic Safety Administration, rage is a key factor in two-
thirds of all fatal car crashes.76 That’s about 28,000 highway deaths each year. In addition, of
course, are the untold numbers of nonfatal accidents caused by tailgating, speeding, weaving,
exchanges of insults, honking, screaming, and actual gunfire.
Issues surrounding caffeine affect each and every one of us. We live, work, and play within a social
framework that depends upon personal interaction. We know that the quality of this interaction
depends to a great extent on the level of harmony, peace, cooperation, patience, and forgiveness we
are able to maintain. We also know that caffeine often works to the detriment of these factors.
• A study of locomotive engineers showed that coffee consumption was linked with
increased negative mood and decreased positive mood.77
• A sample of 144 inmates from a maximum-security penitentiary reported that those who
consumed high levels of caffeine experienced poorer general mood levels than any other
group. Caffeine consumption in this sample population averaged 800 milligrams per day—
well above the amount considered damaging to health.78
• Importantly, there appears to be a time-dose factor in the development of caffeine and
stress-related disorders. The body is able to compensate for increased stress hormone
levels, but not forever. At some point (and this depends on myriad individual factors that
are impossible to predict) the body’s stress management system (known as the
hypothalamic-pituitary-adrenal axis, or HPA) starts to malfunction. This results in a well-
defined breakdown pattern with clear biochemical abnormalities and symptoms of physical
and emotional illness.
Recently, a group of researchers wanted to test the hypothesis that people with borderline
hypertension could be distinguished from those with normal blood pressure simply by looking at the
health of their HPA axis. Sure enough, there was a high correlation between abnormal stress
hormone levels and the incidence of borderline hypertension, proving that a failure of the stress
management system is a factor early in the disease process. Importantly, this biochemical defect also
produced a characteristic alteration of mood and behavior, marked by feelings of exhaustion and
emotional distress. The researchers referred to this condition as “a defeat type of reaction to
stress.”79
The good news is that the converse is also true. There are steps you can take that will reliably
lower your stress hormone levels and even restore balance to the HPA axis. As you well know,
getting off caffeine is an important first step, but yoga, meditation, prayer, tai chi, and biofeedback
can also help a great deal, and have been shown to produce often dramatic improvements in energy
and mood, with decreased tension, decreased anger, and increased feelings of well-being.80, 81
Background Stress—The Saboteur of Health
At this point, you know that there are serious health risks associated with caffeine consumption, and
we have explored many of these in detail. The arguments I present are carefully documented from
the scientific and medical literature. Some health risks are easy to quantify. For example, you can
have the level of cortisol in your blood checked, or you can compare the incidence of various
diseases among coffee drinkers and nondrinkers. But there are more subtle factors at work as well,
what I call disposition and outlook.
The image I get regarding life for most people today is one of pots on a stove. We’re constantly
putting on lids to prevent pots from boiling over, and switching pots to “back burners.” Well, what if
we were able simply to turn down the heat? Wouldn’t that make a great deal of sense? In other
words, life is complex. If you can simplify things (i.e., by taking pots off the stove), good for you.
But sometimes that’s not possible or even desirable, and life remains complex and busy. In that case,
reducing the background level of stress and tension is critically important to maintaining the balance
and quality of your life.
Getting off caffeine is like turning down the heat. Everything becomes more manageable. There
may still be half a dozen pots on the stove, but they’re simmering nicely instead of boiling over.
Once again, the decision is up to you as to which experience of life you desire.
Another View
When I am challenged by representatives of the caffeine industry, their arguments are most often
based upon the lack of scientific consensus regarding caffeine and mental health. I admit that this is
so. There is no universal agreement concerning the effects that caffeine produces in the body or the
mind. But I would like to make two points:
First, no one is arguing that caffeine is good for us. The only debate concerns the degree to
which it is harmful. Second, I would like to suggest looking at the issue from a different angle. Take
the association between caffeine and anxiety disorders. This chapter presents solid and convincing
evidence that caffeine causes anxiety in great numbers of people. In many cases, anxiety affects the
quality of life to the point of producing incapacitating emotional illness such as panic disorder. Still,
there are those who will say the data is not strong enough. To them I put the following question: Do
people suffering from anxiety improve when they reduce or eliminate caffeine?
The answer to this question is a resounding yes. Not only do I know it from clinical experience,
but careful research has also proven the benefits of caffeine reduction. A landmark study published
in the British Journal of Clinical Psychology found that patients suffering from anxiety tend to
consume more caffeine than the general population. In fact, more than one-third of their study group
was categorized as “heavy caffeine users.” After a period of caffeine reduction, these patients saw
their symptoms decrease by a mean of 42 percent and, importantly, the improvement was directly
proportional to the caffeine intake. In other words, those who reduced caffeine a little improved a
little, while those who made very significant reductions in caffeine intake showed the greatest
improvement.82
Take the Challenge!
Most people have no idea what life would be like without the background of caffeine and stress
hormones coursing through their veins. Even if you’re only having a few cups a day, chances are
your personality is affected in ways that may be too subtle for you to associate with caffeine. As
you’ve seen in this chapter, caffeine’s contribution to anxiety and depression alone are reasons
enough to kick the habit.
I want to encourage you to conduct a trial period without caffeine. You owe it to yourself. Use
the Off the Bean program in Chapter 10 to break the habit. Remember that you must go through the
entire detoxifying process, which takes a minimum of three weeks, before you can begin to measure
the results—and that it takes sixty days total before you can fully assess the benefits of being
caffeine free.
Assure yourself that if you don’t feel significantly better, you can always go back to caffeine.
But at least you’ll know that you explored the option, and are not simply a slave to the coffeepot.
Not only your mood, but your entire outlook on life, stands to benefit as a result.
CHAPTER 5
Specific Health Disorders: The Caffeine Connection
Caffeine and Cardiovascular Disease
I know, you’ve heard it a thousand times: Cardiovascular disease is the nation’s number one killer.
But have you ever thought about what that actually means? If we translate the abstract numbers into
concrete terms, the picture becomes much more real and immediate. Only then will we be motivated
to do something about it—in our own lives and in the lives of those we love.
Cardiovascular disease (CVD) encompasses disorders of the heart and blood vessels, including
heart attack, stroke, chest pain, hypertension, rheumatic heart disease, and atherosclerosis
(hardening or blockage of the arteries). In 1997, more than 960,000 Americans died of
cardiovascular disease. Remarkably, there are societies on earth where CVD is rather rare, so we
know that it’s not one of the inevitable consequences of aging. In fact, CVD is preventable.
Nevertheless, unless people take action toward prevention, things will go on just as they have for
decades.
In America today, nearly one-third of men between the ages of fifty and sixty will die within the
next ten years from cardiovascular disease. And if that surprises you, consider that this disease now
kills more women than men. More people die of cardiovascular disease than succumb to all cancers,
all accidents, pneumonia, influenza, suicide, and AIDS combined: one life every thirty-three
seconds.1
HEART DISEASE
Coronary heart disease (or heart disease) is by far the most common form of cardiovascular disease.
According to the American Heart Association, every twenty seconds, an American suffers a heart
attack, and every sixty seconds somebody dies from one. If you picked up your morning paper and
read that three jumbo jets had crashed the day before, you would be greatly alarmed. What if this
happened every morning, 365 days a year? That’s the impact heart disease has on our nation, and
yet the efforts at prevention are limited. Sure, there have been significant advances in hospital
coronary care units, and more people are trained in CPR, but that’s not prevention—that’s simply
rapid response.
The goal, after all, is to prevent heart attacks, and present efforts toward that end fall into two
categories: drugs and dietary change to lower cholesterol, and drugs and dietary change to lower
blood pressure. As valuable as these measures are, they are still not primary prevention. What about
preventing cholesterol levels and blood pressure from rising in the first place, and what about all of
the other risk factors in heart disease?
Given a complex issue, people (especially the media) naturally look for a simple explanation.
Heart disease was thus reduced to a “cholesterol problem,” which of course turned out to be untrue.
Plenty of people have high cholesterol and never have heart attacks, and every day people with low
cholesterol are rushed to the hospital in cardiac arrest.
Even adding the blood pressure factor does not produce an accurate picture of heart disease, but
these two considerations are the only ones that receive much attention. And since coffee-induced
increases in cholesterol and bipod pressure appear to be relatively small, the professional and
popular press have written off coffee as a risk factor. But nothing could be farther from the truth.
“The strong association between coffee consumption and coronary heart disease
risk found in several different studies and the implications for the large population at
risk are compelling arguments for concern about adverse cardiovascular effects of
caffeine consumption.”
Source: Neal L. Benowitz, M.D., “Clinical Pharmacology of Caffeine,” Annual
Review of Medicine, 1990;4l:277–88.
CHECK YOUR PRESSURE
First of all, increases in blood pressure due to caffeine are often quite significant. Even in moderate
doses, caffeine can raise blood pressure in healthy young men and women to the level of borderline
hypertension.2, 3 In those with existing hypertension, caffeine can be even more dangerous. The key
factor, once again, is stress.
The first hint of this intriguing phenomenon came in 1969, when researchers tested caffeine’s
effect on blood pressure in rats. They found that caffeine produced only modest increases in blood
pressure and were about to write it off; but they decided to repeat the experiment on stressed rats.
Sure enough, when the rats were given caffeine and then placed in a crowded situation (i.e., under
stress), their blood pressure increased dramatically.4
Since then, the same pattern has been identified in humans. When subjects are relaxed, caffeine
does not appear to raise blood pressure significantly. These are the studies most often cited by the
caffeine industry. But is this an accurate representation of most people’s lives? Real life is stressful,
and caffeine multiplies the increase in blood pressure and the subsequent damage.5
Throughout this book, I have emphasized the point that any evaluation of caffeine must look
carefully at those who are most vulnerable. In this regard, recent research on men with borderline
hypertension is quite revealing. It was found that in this group, the increase in blood pressure after
ingestion of caffeine was greater than that found with healthy controls. What’s more, this group also
had an exaggerated response to caffeine combined with a stressful task.6 In other words, caffeine
intake is most dangerous for those who are most vulnerable (read: most stressed), a pattern that we
will see numerous times in subsequent chapters.
HABITUAL COFFEE DRinkers: ALSO AT RISK
It was long believed that habitual coffee drinkers did not suffer the increased blood pressure seen
when caffeine is administered to non–coffee drinkers. Recent research, however, has revealed that
caffeine can affect blood pressure in just about anyone.7 One study with sixty “heavy” coffee
drinkers found that caffeine continued to cause increases in blood pressure, and the authors
emphasized in their conclusion that these effects “do not appear to habituate with regular use.”8
As it turns out, the hypertensive effects of caffeine appear to be related to changes in blood
caffeine levels. While habitual drinkers tend to maintain levels of caffeine through repeated doses
throughout the day, these levels drop during sleep. In other words, the lower a person’s caffeine
level first thing in the morning, the greater the hypertensive effect of those first few cups of coffee.
Experts estimate that at least 25 percent of the general population has early-morning blood levels of
caffeine low enough for normal caffeine consumption to raise their blood pressure.9
Now, this brings up a very intriguing point. According to national health statistics, an individual
is more than 50 percent more likely to have a heart attack on a Monday than on a Saturday. At first,
everyone took this as simple evidence that Mondays are high-stress days and Saturdays are relaxed
days. But researchers were surprised to find that the pattern held even among those with low-stress
jobs. It turns out that caffeine is the critical factor. Since most people consume less coffee on the
weekends, a coffee drinker’s blood caffeine level will tend to be lowest on Monday morning, just
when he or she is likely to slam down the most coffee. The resulting increase in blood pressure,
while temporary and unlikely to show up in a scientific study, may well prove fatal.
“The cardiovascular effects of caffeine may persist throughout the day with
repeated administration of moderate amounts of caffeine. Habitual caffeine use
does not necessarily lead to complete tolerance, which suggests that caffeine’s
cardiovascular effects could contribute to an increased risk of cardiovascular
disease.”
Source: J. D. Lane and D. C. Manus, “Persistent Cardiovascular Effects with
Repeated Caffeine Administration,” Psychosomatic Medicine, July–August
1989;51(4):373–80
RESEARCH CAPSULE
Diet Pills and Caffeine: A Deadly Duo
Prior to the Controlled Substances Act of 1970, most diet pills contained
amphetamine drugs, which effectively suppress appetite but cause addiction and
dangerous side effects. When the FDA banned amphetamines, manufacturers
created similar effects (and side effects) with the combination of two central
nervous system stimulants, caffeine and phenyl-propanolamine (PPA). In the mid-
1980s, the FDA moved against this dangerous mix because of a number of deaths
associated with its use. Too late for some users, research found that while both
drugs alone increase blood pressure, the combination of caffeine and PPA could
result in massive increases, triggering stroke and heart attack.10–11, 12, 13 That’s
why today the active ingredient in most diet pills available without a prescription is
phenylpropanolamine alone.
However, while caffeine-PPA combinations may be banned, people using PPA
diet pills still drink coffee, sometimes lots of coffee. What’s more, PPA is frequently
overused. The reasons for this become clear once you understand how PPA works.
Again, it’s related to stress hormones, this time norepinephrine.
As described in Chapter 2, norepinephrine (NE) is a powerful biochemical
produced in the adrenals and nervous system that affects mind, mood, and
behavior. PPA (like amphetamines) causes a rapid release of NE, which creates
stress but feels like “energy.” NE also suppresses appetite. The problem is that
amphetamines and PPA do not increase the brain’s synthesis of NE. If you’re
releasing more NE but you’re not replacing NE stores in the brain, you will
ultimately experience a rebound “letdown.” As brain levels of NE fall, users must
take more and more PPA to experience the same amount of appetite suppression.
Such overuse may not only raise blood pressure, but also cause insomnia,
irritability, headache, anxiety, and panic. When caffeine is added to the equation,
the likelihood (and severity) of adverse effects is multiplied, due most likely to the
fact that PPA can produce dramatic increases in blood caffeine levels.14 Cases
have been reported where individuals suffered manic psychosis after ingesting
caffeine and PPA.15
“The effects of the widely consumed drugs caffeine and phenylpropanolamine
are mediated through activation of the central and sympathetic nervous systems.
Severe, life-threatening, and occasionally fatal hypertensive reactions have been
reported after their combined use.”
Source: C. R. Lake, D. B. Rosenberg, S. Gallant et al., “Phenylpropanolamine
Increases Plasma Caffeine Levels,” Clinical Pharmacology and Therapeutics, June
1990; 47(6):675–85.
THE WHOLE STORY
Most people assume that caffeine raises blood pressure because it makes your heart beat faster or
harder. If this were the case, you would expect your blood pressure to return to normal fairly soon
after a cup of coffee—and that doesn’t happen. The fact is that caffeine causes vascular resistance, a
condition in which the blood vessels (especially in the extremities) constrict and reduce blood
flow.16 This stress response was very useful a few thousand years ago in the face of imminent
physical harm. Vascular resistance reduced blood loss from injuries. But today all it does is raise
your blood pressure and make your fingers cold.
Actually, vascular resistance affects many areas of the body and mind. As discussed in the
previous chapter, caffeine reduces circulation in certain areas of the brain. Once again, the fight-or-
flight/survival part of the brain remains unaffected, but areas associated with long-term memory and
learning can be impaired.
Put on your physiology hat. Can you think of another condition in which vascular resistance
could cause a major problem? How about the increased circulation associated with exercise? Here
the muscles are working hard and starved for oxygen and fuel. Under conditions of vascular
resistance, the entire system can go into hyperdrive, elevating blood pressure much higher than it
would be at rest. A study with healthy young men (none of whom had high blood pressure)
published in the American Journal of Cardiology showed that a modest amount of caffeine taken
before exercise produced dangerous elevations in blood pressure in 45 percent of subjects.17 When a
similar experiment was conducted with men at risk for hypertension, the results were even more
alarming.18
THE CALCIUM CONNECTION
Research has identified an important connection between calcium metabolism and hypertension,
accounting for the fact that calcium supplementation lowers blood pressure in about 25 percent of
patients. Because caffeine is known to disturb calcium metabolism, a study was recently conducted
to explore the effects of caffeine abstinence on blood pressure. The results? After two weeks off
caffeine, two important measures of calcium status (serus ultrafiltrable calcium and parathyroid
hormone) improved markedly in nearly all of the subjects.19 These results illustrate clearly that
caffeine stresses calcium metabolism, and that those desiring to control their blood pressure would
do well to get “off the bean.”
CHECK YOUR OIL
Scores of studies have been performed to evaluate the effects of coffee and caffeine on blood
cholesterol levels. Most have found that coffee (including decaf) is associated with elevated
cholesterol, and these increases are not always small.20–21, 22 In fact, blood cholesterol levels appear
to rise in direct proportion to the number of cups of coffee consumed,23–24, 25, 26, 27, 28, 29 and we
now know what causes this rise in blood cholesterol. It’s not the caffeine, as once thought, but two
other chemicals (diterpene alcohols) naturally found in coffee: cufestol and kahweol.30, 31
How does all this impact coronary artery disease? Most experts today agree that for every 5
percent increase in serum cholesterol over 200 milligrams per deciliter, there is a 10 percent increase
in risk for heart attack or stroke. That means that stress and coffee can make a tremendous
difference in your risk for these killer diseases. What’s more, coffee intake is associated with
elevations of the most dangerous fraction of cholesterol, known as apolipoprotein B, and this
correlation has been found at moderate intake of two or more cups per day.32
BEYOND BLOOD PRESSURE AND CHOLESTEROL
As I mentioned, the caffeine/cardiovascular disease debate has, until recently, been limited mainly
to a discussion of blood pressure and cholesterol. Since there is no universal agreement on how
much these risk factors are raised by caffeine, it has been possible for the caffeine industry to duck
the entire issue. But no more.
That’s because six additional risk factors are coming to light, and caffeine is involved in each
and every one.
“One point most authorities do agree on: Patients prone to cardiac arrhythmias
should avoid caffeine. The amount in just a few cups of coffee can cause
problems.”
Source: Paul Cerrato, B.S., M.A., Journal for the American Association of Office
Nurses.
1. ARRHYTHMIA AND BLUES
The proper function of the heart as a pump depends upon an intricate series of electrical impulses
that contract chambers and open valves in perfect timing. This rhythm is the pace of life, sending
blood continuously to more than 75 trillion cells in your body.
When the heart muscle is stimulated out of the proper ***********time sequence, pumping
action becomes uncoordinated and blood flow becomes weak. If proper rhythm is not restored, these
conduction and rhythm disturbances (collectively called arrhythmias) are usually fatal. Scientists do
not understand exactly what causes arrhythmias, but they do agree that caffeine is associated with
increased risk among those prone to the disorder.33, 34It is also important to note that the amount of
caffeine required to disturb heart rhythm is not great. Intake of less than 300 milligrams per day has
been associated with greater incidence of arrhythmias.35, 36 Since a fourteen-ounce mug of coffee
contains around 200 milligrams of caffeine, less than two mugs can easily put you into the increased
risk category.
Even in healthy individuals, the combination of stress and fatigue has been shown to increase
risk for arrhythmias.37 Think about that. When you’re feeling beat, haven’t slept well, or you’re just
pushing too hard, how often do you resort to drinking coffee to get through the day? The resulting
strain on your heart can be significant. Caffeine can also cause tachycardia (rapid heartbeat) and can
exacerbate the symptoms of mitral valve prolapse (MVP), a common heart defect. In fact, MVP
may be an important key in our understanding of the arrhythmia-caffeine connection.
Mitral Valve Prolapse (MVP)
The mitral valve lies within the heart, regulating the flow of blood from the left atrium to the left
ventricle. When the valve is prolapsed (fallen or weakened), it malfunctions, and as the heart beats,
blood may flow back into the atrium. MVP is rarely serious, but it does produce occasional or
periodic symptoms, including shortness of breath, fatigue, light-headedness, and dizzy spells. The
cause is unknown, but there is a significant genetic factor. Individuals with one affected parent have
a 50 percent chance of inheriting MVP.
While MVP can cause heart murmur, palpitations, and chest pain, most individuals with the
disorder have no noticeable symptoms and are unaware of the condition. Still, MVP significantly
increases one’s risk for arrhythmia,38, 39 and the combination of caffeine and MVP can be
dangerous. Interestingly, caffeine researchers often remove individuals with MVP from their
investigations, presumably because such individuals would exhibit negative effects greater than the
average person. But that’s bad science. Conservative estimates are that 7 to 10 percent of the
population has MVP. That’s millions of Americans, and these are precisely the people who should
be studied because they are among the most vulnerable to caffeine’s adverse effects.
Aside from mitral valve prolapse, there are other arrhythmia risk factors that appear to operate
in conjunction with caffeine intake. Caffeine can cause a sudden contraction of the aortic muscle, as
well as dramatically increased stress hormone release in the heart itself. In an individual whose
arteries are already partially blocked, such events can produce arrhythmia and heart attack.40
There are also reports that caffeine can increase the incidence of paroxysmal atrial tachycardia
(PAT) and ventricular beats, other types of heart rhythm disturbance. These arrhythmias are often
associated with exertion, and doctors have reported increased incidence of PAT with caffeine (coffee
or tea) when taken as much as twelve hours prior to exercise.41
This brings up an important point concerning caffeine research: Long-term effects are often
ignored. After all, you only see what you’re looking for. But new research using continual heart
monitoring technology enables us to look at the full spectrum of caffeine effects, including
something known as heart rate variability (HRV). HRV has been shown to correlate very strongly
with sudden death, and while moderate caffeine ingestion appears to produce no abnormal HRV in
young adults, it has been shown to aggravate abnormal HRV in overweight, middle-aged subjects.42
“There is a two times (200 percent) greater likelihood of ventricular premature beats
after coffee ingestion.”
Source: T. K. Leonard, R. R. Watson, and M. E. Mohs, “The Effects of Caffeine on
Various Body Systems: A Review,” Journal of the American Dietetic Association,
1987;87(8):1048–53.
2. CORONARY VASOSPASM
When an artery is blocked, tissue beyond the block is deprived of oxygen and quickly dies. If this
occurs in an artery leading to the heart, it causes a heart attack (medical term: myocardial infarct or
MI). If the block is in an artery leading to the brain, it causes a stroke. In both cases, the major cause
of blockage is the narrowing of an artery from the buildup of plaque, a process known as
atherosclerosis. Often, the fatal combination is atherosclerosis and a blood clot that lodges in the
narrowed artery.
But in approximately 20 percent of fatal heart attacks, an autopsy reveals that the victim had
clear arteries. What caused the blockage of blood (and therefore oxygen) to the heart resulting in
massive cell death and heart attack? Often it is a spasm of one or more arteries leading to the heart.
Known as coronary vasospasm, this event can shut off blood supply as effectively as a clot or
atherosclerosis.43 You need to know that the risk for such a tragedy is related in part to your intake
of caffeine.
In fact, caffeine contributes to coronary vasospasm in multiple ways. We know that caffeine, by
stimulating the release of stress hormones, lowers the stress threshold (review Chapter 3) so that
situations that would otherwise have been handled become distressful. With this caffeine-induced
stress “magnifier,” the risk of vasospasm is increased.44
Caffeine also contributes to magnesium deficiency, a condition that makes arteries more prone
to spasm.45 In typical vicious-cycle fashion, the combination of caffeine and stress exacerbates the
low magnesium state.46 What’s more, if there is also a buildup of plaque within the artery, the
tendency for arteries to spasm increases the overall risk for heart attack tremendously.
On the other hand, it is important to understand that the entire scenario of magnesium
deficiency, elevated stress hormones, and hypersensitive arteries can be silent. You don’t feel any of
these dangerous developments like you would, for example, if your arteries were being occluded by
plaque. In those cases, there are often clear warning signs such as breathlessness upon exertion or
chest pain. But research shows that a person prone to vasospasm can have a completely normal
electrocardiogram and be symptom-free47—that is, until they end up facedown on the sidewalk after
their morning jog.
3. HOMOCYSTEINE
Early in 1997 the American Journal of Clinical Nutrition published research confirming a strong
association between coffee consumption and elevated blood levels of a biochemical known as
homocysteine.48 Elevated homocysteine is a powerful contributor not only to heart disease, but also
to stroke, miscarriage, birth defects, and possibly Alzheimer’s disease. And the data is
incontrovertible. A huge study group (over 16,000 people), almost equally divided between men and
women, was evaluated, and the researchers were careful to factor out variables like smoking,
vitamin intake, and history of cardiovascular disease. The study’s conclusion is definitive and
crystal clear: As coffee intake increases, so does the level of dangerous homocysteine in the blood.
But when I went on-line to see what my cardiologist colleagues were planning to do about this
remarkable data, I found only stony silence. The consensus of opinion was to “wait for more
information.” In other words, no medical organization was even going to mention this report to their
members, let alone recommend moderation of coffee intake
More Information Comes In
A few months after the coffee and homocysteine report appeared the Journal of the American
Medical Association (JAMA) published another landmark study, this one looking at homocysteine
and heart disease.49 Turns out the homocysteine factor is far more important than anyone thought. In
fact, the JAMA study concluded that, in terms of risk for cardiovascular disease, elevated
homocysteine is “equivalent to [high cholesterol] or smoking.” People with the highest
homocysteine levels had more than three times the risk for cardiovascular disease than those with
low homocysteine.
There are now over fifty studies that illustrate precisely how homocysteine increases your risk
of cardiovascular disease. While this is not the place for a detailed lesson in physiology, I’m not
sure you’ll be hearing anything about the matter soon from your doctor, and it’s too important to
ignore. This information could very well save your life (or at least a painful and expensive trip to
the hospital).
You know that proteins are composed of amino acids. One of those amino acids, methionine, is
commonly found in meat and dairy products, and when the body processes or metabolizes
methionine, homocysteine is created as a byproduct. Normally, the body breaks down the
homocysteine into harmless metabolites, but there are a number of factors that either prevent this
breakdown or overwhelm the body’s ability to clear homocysteine from the blood.
Caffeine raises homocysteine levels in two ways. We know that the elimination of homocysteine
from the blood requires optimal amounts of folic acid, vitamin B-12, and vitamin B-6. Caffeine
depletes these vital nutrients. Secondly, caffeine appears to interfere with the normal breakdown of
homocysteine. A diet high in meat and dairy products, on the other hand, tends to overload the
system. Combine the two and you have real trouble. Add smoking to the mix and you’re a walking
time bomb.
What Exactly Does Homocysteine Do to the Body?
Research suggests that homocysteine damages blood vessel walls. These injury sites, known as
lesions, start to collect the substances your body sends to repair the damage. This material builds up
over time, accumulating protein, calcium, and cholesterol from the bloodstream and forming plaque,
which ultimately blocks the artery.
Other researchers have found that homocysteine increases the stickiness of platelets, cells in the
blood that are essential for clotting. As platelets become more sticky, the likelihood of abnormal clot
formation (and subsequent stroke or heart attack) increases dramatically.
Elevated homocysteine also affects the blood vessels’ ability to dilate. Remember that every
time your heart beats, your arteries must expand (dilate) to accommodate the increased pressure. As
homocysteine levels increase, however, the blood vessels lose this elastic ability and are damaged as
a result.50 Consider that as we age, most people’s overall blood pressure increases.
Consider also the damage done to rigid blood vessels under conditions of strenuous exercise.
Normally, blood pressure rises and arteries expand to meet the body’s increased need for oxygen
and fuel. But when homocysteine levels are high, blood pressure increases and the blood vessels
don’t expand. The result: accelerated damage, cardiovascular disease, and increased risk for heart
attack and stroke.
Who’s at Risk?
While all caffeine users are at increased risk for elevated homocysteine, the following groups have
been identified as very high-risk populations.
1. People with other risk factors. If you have high blood pressure or high cholesterol, or if
you smoke, even a small increase in homocysteine will greatly increase your risk of
cardiovascular disease.51
2. Diabetics. People with diabetes are at increased risk because homocysteine appears to be
far more damaging to their blood vessels. What’s more, they have reduced ability to clear
homocysteine from their bodies. This greatly increases risk for heart disease, as well as
degeneration of the eyes and peripheral circulation.52, 53 In fact, there are a number of
reasons why diabetics should not drink coffee (see list on pages 199–200).
3. People with rheumatoid arthritis. Recent research has shown that people with rheumatoid
arthritis also have a defect in homocysteine metabolism that makes them particularly
vulnerable to even slight elevations of this biochemical.54 That may account for the
observation that people with rheumatoid arthritis often improve on a vegan diet (no meat,
eggs, or dairy), which is naturally low in methionine.
4. People with a family history of Alzheimer’s disease. Alzheimer’s disease is also
characterized by abnormally high homocysteine levels.55 While a cause-and-effect
relationship has not been confirmed, the rationale for homocysteine-induced brain
degeneration is not far-fetched. Homocysteine appears to accelerate free radical activity, a
process known to damage nerve cells.
5. The elderly. Studies indicate that as many as 50 percent of individuals over age sixty-five
have elevated levels of homocysteine.56 Coffee drinkers in this group are therefore likely to
have far more serious consequences than they might have experienced in their younger
years.
What’s Being Done?
As far as I can see (and I’ve looked extensively), nothing is being done. A review article on the
health effects of coffee was published in the Medical Tribune on June 25, 1997.57 This magazine is
read by more physicians than any other medical publication. The word homocysteine did not appear
in the article. Instead, the American Heart Association was quoted as saying, “[M]oderate coffee
consumption does not appear to increase a person’s risk of heart attack.” In their current publication
dealing with caffeine, the AHA statement is even worse: “Whether or not high intakes of caffeine
increase the risk of coronary heart disease is still under study” (my italics).
In reality, the caffeine-homocysteine-heart disease connection has been thoroughly and
exhaustively examined. Conclusive research has even been published in the AHA’s own journals!58
It’s just that no one appears to be willing to draw the obvious and important conclusions from the
mountain of data already in hand.
RESEARCH CAPSULE
You’ve heard about HDL (high-density lipoprotein), the “good” cholesterol that lowers your
risk of heart disease? Your doctor may have encouraged you to exercise regularly in order to raise
the level of this protective factor. Well, if your homocysteine levels are high, all the HDL in the
world won’t protect you. Research just published in the American Journal of Cardiology shows that
homocysteine is so damaging that it virtually eliminates any protective benefits obtained from high
HDL.
Source: H. R. Superko, “Elevated High-density Lipoprotein Cholesterol Not
Protective in the Presence of Homocysteinemia,” American Journal of Cardiology,
March 1, 1997;79(5):705–06.
Three Steps You Can Take
Research appearing in the pages of dozens of medical journals now supports a prudent and effective
approach to reducing your blood levels of homocysteine. You’re not likely to read about these steps
in a magazine or hear about them on the evening news. You probably won’t hear them from your
doctor, and that’s because these important measures do not involve the purchase of expensive,
patented drugs. Instead, they involve three simple steps:
1. Decrease your intake of meat and dairy products, and increase fresh fruits and vegetables.
2. Decrease or eliminate your intake of coffee.
3. Take a daily vitamin supplement that provides 400 micrograms of folic acid, 20
micrograms of vitamin B-12, and at least 5 milligrams of vitamin B-6.
A+B = Huh?
A: “We conclude that an elevated homocysteine level is now established as a strong and
independent factor associated with all categories of atherosclerotic disease in both men and
women.”
Source: I. M. Graham, L. Daly, Helga Refsum et al., “Plasma Homocysteine as a
Risk Factor for Vascular Disease: The European Concerted Action Project,” Journal
of the American Medical Association, 1997;277:1775–81.
B: “In conclusion, we found a strong dose-response relation between coffee intake
and plasma homocysteine concentration. … Given the widespread use of coffee,
even small adverse consequences will have important health implications.”
Source: O. Nygard, H. Refsum et al., “Coffee Consumption and Plasma Total
Homocysteine: The Hordaland Homocysteine Study,” American Journal of Clinical
Nutrition, 1997;65:136–43.
C: “[M]oderate coffee consumption does not appear to increase a person’s risk of
heart attack.”
Source: American Heart Association
4. HOSTILITY AND ANGER
Numerous studies have shown that hostility and anger significantly increase risk for heart disease
and stroke.59 We now know that these emotions are tied to stress hormones in a vicious cycle:
Anxiety and stress cause increased production of epinephrine and cortisol, which then affect mood,
mind, and behavior in such a way as to create more stress, hostility, and anger. A common trigger?
Caffeine.60
Importantly, the damage caused by the additive effects of caffeine and stress is often silent.
Small arteries may spasm, cutting off blood supply to vital areas of the heart for short periods of
time. The risk for rapid heartbeat (tachycardia), flutter, and arrhythmias all increase during periods
of intense stress, but the victim, caught in the emotional spiral, is often completely unaware of the
damage being done.
As you can imagine, one outburst of anger is not likely to give you a heart attack. The research
is conclusive, however, regarding people in whom hostility and anger are common experience. At
different points in life, we may find ourselves in jobs or situations that stimulate anger and
aggressiveness. Ironically, those are also the times when we tend to drink the most coffee. Breaking
this destructive cycle, therefore, involves changing our habits and awareness.
“We have found that anger can cause a weakness in the pumping action of the
heart.”
Source: G. Segall, M.D., of Stanford University, Medical Tribune, 1991;32(14):17.
5. THE MAGNESIUM CONNECTION
Adequate magnesium is essential for normal heart function and even a slight deficiency of this
mineral can have adverse effects on the heart and blood vessels. Diet surveys and blood tests show
that millions of people consuming a typical American diet are not obtaining sufficient magnesium
from their food.61, 62 Most of them are also drinking coffee, which has been shown to deplete
magnesium from the body.63, 64 You don’t have to be a Ph.D. in public health to see that this is a
major problem. Low magnesium increases the risk for arrhythmia, congestive heart failure, heart
attack, coronary vasospasm, hypertension, and stroke.65–66, 67> One recent report in the American
Heart Journal noted that “the intricate role of magnesium on a biochemical and cellular level in
cardiac cells is crucial in maintaining stable cardiovascular function.”68
“It should be realized that preventing the patient from a magnesium deficit is the
first, and the application of magnesium the second best strategy to keep the patient
free from cardiac arrhythmias.”
Source: M. Zehender, “Magnesium as an Anti-arrhythmic Therapy Principle in
Supraventricular and Ventricular Cardiac Arrhythmias,” [German], Zeitschrist for
Kardiologie, 1996;85 supplement 6:135–45.
Here is yet another vicious cycle. Research shows that Type A individuals (high-stress
personalities) lose significant amounts of magnesium when faced with a stressful situation
compared to Type B individuals (easygoing personalities.)69 But we also know that Type A people
tend to drink a great deal more coffee than Type B folks. And it doesn’t really matter which factor
comes first (stress or caffeine intake). The result is that the people who need magnesium the most
are the ones whose stores are most depleted.
When was the last time your doctor measured your magnesium level? Chances are it never
happened, even if you are at risk for heart disease. Once again, that’s because nutrition, diet, and
exercise are usually overlooked in favor of the “quick-fix,” drug-oriented approach. Some blood
panels measure serum magnesium, but that reflects only the amount of the mineral that was being
transported in your blood at the time the test was taken. It does not indicate the amount of
magnesium in your body. You can obtain that important information by measuring the magnesium
in red blood cells. Known as RBC magnesium, this valuable test can be done by most laboratories,
but you’ll have to ask for it and pay for it yourself. Insurance companies, for the most part, do not
yet understand the remarkable preventive benefit of maintaining optimal levels of magnesium, even
though the data has been available for twenty years.
A special note for individuals with any form of heart disease: A new study has
conclusively shown that oral supplementation with magnesium can significantly
reduce the incidence of arrhythmia.70 This does not mean, however, that you can
drink all the coffee you want and simply take a magnesium pill. Coffee will deplete
magnesium rapidly, even from a supplement, and increase your risk for heart
disease in multiple ways. A sensible strategy for staying alive and healthy:
Decrease or eliminate caffeine. Supplement with a high-potency multimineral
providing at least 400 milligrams of magnesium and 100 milligrams of potassium
per day.
6. ALTERED BLOOD CLOTTING
When a person is killed by a stroke or heart attack, there are always direct and indirect causes.
We’ve been discussing the indirect causes, those factors that contribute to the blockage of an artery.
But the direct cause (the blocked artery) is also fairly complex, insofar as arteries do not usually
build up sufficient plaque to stop all blood flow. The killer factor is often a blood clot that travels to
the narrowed artery and plugs it up.
Today, it is common for people with atherosclerosis to be given “blood thinners,” drugs that
decrease the clotting ability of the blood. The fact is, however, that millions of Americans are
walking around with what is known as silent ischemia. Plaque has built up in their arteries, but not
to the point of causing pain or abnormal heart activity. Health experts are concerned because the
number of people with silent ischemia is increasing dramatically, and not just because the baby
boomers are reaching their fifties. The most frightening thing is that this condition is being
diagnosed in people who are in their thirties and forties.
Silent ischemia is “an accident waiting to happen.” If a person should form an abnormal clot
and if that clot finds its way into a narrowed artery leading to the heart or brain, he or she is
finished. You need to remember that in a large percentage of cases, the first sign of cardiovascular
disease is a fatal heart attack.
Anyone who has owned a house will tell you that plumbing requires regular maintenance, and
even then, after thirty or forty years, large sections may have to be replaced. And that’s steel and
copper pipe. Your plumbing (over 1,000 miles of blood vessels) is delicate tissue, subject to the
same forces of pressure, erosion, wear, and tear. And the way the body fixes leaks involves clotting.
You might not know that in addition to the cuts, punctures, nicks, and scrapes that are visible signs
of clotting, you spring internal, invisible “leaks” on a regular basis, and your body fixes itself
remarkably—like having a self-repairing plumbing system in your house.
But this mechanism must be finely tuned. If your blood clots too slowly, you can hemorrhage. If
your blood clots too fast, you’ll tend to form unnecessary clots that can wreak havoc in the body.
Interestingly, the clotting mechanism is very much affected by what we eat and drink. A diet high in
meat and dairy products will tend to increase the “stickiness” of your platelets, thereby making your
blood more likely to clot abnormally fast.
I started wondering about the effect of coffee on blood clotting when I was studying the stress
response. We know that adrenaline accelerates blood clotting, and from an evolutionary point of
view, this makes perfect sense. After all, throughout human history, the events that got our
adrenaline up were threats to our survival, and those threats often resulted in injury. The stress
response thus produces alterations in the blood to make it clot faster.
But today, as I have explained, stress is remarkably different. Instead of facing a saber-toothed
tiger or a club-wielding foe, we’re facing deadlines, crammed schedules, traffic jams, and mortgage
payments. None of these involve physical injury, but we cannot change our genes. Stress still
produces alterations in blood clotting, and on top of this, millions of people accelerate the clotting
mechanism of their blood every morning when they slam down their first cup of coffee.
Caffeine actually appears to affect blood clotting in two ways: by magnifying the normal stress
response (resulting in higher stress hormone levels), and by raising homocysteine levels (see “3.
Homocysteine,” this chapter). This may account for a large part of the increased risk for stroke
associated with coffee drinking.
A group of investigators reporting in the American Journal of Epidemiology found a strong
association between caffeine and heart disease. In fact, the increased risk for heart attack was seen
starting at one to two cups of coffee per day.71 At that modest level of consumption, the risk for
heart attack increased 40 percent. In men who drank at least five cups per day, the increased risk
was 200 percent or more.
The data regarding risk for women is even more serious. One recent study examining dietary
factors and heart disease found that the association between caffeine intake and heart attack was
stronger than that for meat, butter, and total fat. In fact, coffee drinkers had almost twice the risk of
heart attack compared to women who did not drink coffee.72 Research by other investigators has
found that consuming more than thirty-six ounces of coffee per day caused a 250 percent increase in
the risk of heart attack in women.73
By looking at individual risk factors for heart disease, the caffeine industry has been able to
snow the public and even most of the medical community. But real people do not have single risk
factors; they have multiple risk factors, and there is an additive or even a multiplying effect when
they are all considered.74 One important study, for example, found that women consuming more
than twenty-four ounces of coffee per day had almost twice the risk of heart attack compared to
non–coffee drinkers. That’s fairly alarming, but when the researchers looked at the combination of
caffeine consumption and elevated cholesterol, coffee drinkers faced astounding odds. Moderate
coffee drinkers with high cholesterol had more than seven times the risk of heart attack, while heavy
coffee drinkers had eighteen times the risk of non–coffee drinkers.75
Likewise, when measured at rest, caffeine raises blood pressure only a little. But when you add
stress (either physical or mental), caffeine can raise blood pressure significantly.76 Caffeine has also
been shown to increase stress hormone release in the heart muscle. If this is viewed as a single risk
factor, the data is not that alarming. But tens of millions of Americans have partial blockage of their
coronary arteries, which produces decreased blood flow or ischemia. When this factor is included, a
different picture emerges. One group of researchers has stated that a modest intake of caffeine in an
individual with ischemia might product a three to six-fold increase in cardiac stress hormones. They
conclude, “We hypothesize that [this release of stress hormones] lies behind the reported connection
between cardiac events and methylxanthines, for instance sudden cardiac death following coffee
consumption.”77
THE ADDITIVE EFFECT OF CORONARY RISK FACTORS
Complete this checklist to see if caffeine is likely to increase your risk for cardiovascular disease:
YES NO
1. Has anyone in your family suffered from heart disease? _______ _______
2. Are you a woman? _______ _______
3. Do you have mitral valve prolapse? _______ _______
4. Is one of your birth parents a diabetic? _______ _______
5. Do you smoke? _______ _______
6. Are you overweight? _______ _______
7. Are you under a significant amount of stress at home or work? _______ _______
8. Have you ever noticed that your heart beats faster after consuming coffee? _______ _______
9. Have you ever noticed any irregularity in your heartbeat, such as the sensation
_______ _______
that it “skipped a beat”?
10. Do you have high blood pressure? _______ _______
11. Does (did) either of your parents have high blood pressure? _______ _______
12. Is your cholesterol level greater than 180 milligrams per deciliter? _______ _______
13. Have you ever experienced ringing in the ears for any length of time? _______ _______
14. Have you ever been diagnosed with transient ischemic attacks (TIAs)? _______ _______
15. Have you ever found that you were out of breath just climbing a flight of
_______ _______
stairs
Key
2–4 “yes” answers: Caffeine will increase your risk for cardiovascular disease.
5–7 “yes” answers: Caffeine will seriously increase your risk for cardiovascular disease.
8 or more “yes” answers: Research suggests that caffeine could be the precipitating factor in your
premature death.
Here is a typical situation in which blood levels of homocysteine (and nutrition in general) are all
but ignored. A fifty-two-year-old man goes to his doctor for a physical. He’s slightly overweight,
and his cholesterol and blood pressure are too high. (By the way, this describes about 30 million
American men.) The doctor writes a prescription for drugs to lower the patient’s cholesterol and
blood pressure, and sends him home.
The problem is that these drugs have significant side effects, not the least of which is decreased
sex drive and fatigue (just what a fifty-two-year-old man does not need). In fact, there is good
evidence that aggressive use of drugs to lower cholesterol and blood pressure actually increases
overall mortality, but that’s another (sad) story. The point I want to make is that prescribing drugs is
not the same thing as health care. In this case, significant factors related to this man’s condition
were completely ignored.
This man needed diet and lifestyle counseling and follow-up. Research shows conclusively that
a low-fat diet combined with stress reduction can dramatically reduce the risk of cardiovascular
disease, and may even reverse CHD damage.78
For someone with high cholesterol and high blood pressure, knowing his homocysteine and
magnesium levels is also critically important. Studies show that supplemental vitamins B-6, B-12,
and folk acid can lower homocysteine.79, 80 Obviously, a magnesium supplement can improve tissue
levels of that vital mineral. We know that coffee raises homocysteine and lowers magnesium. Real
health care would include recommendations for this patient to reduce or eliminate coffee and
supplement his diet with a good high-potency multivitamin. Since that multivitamin would also
include important antioxidant vitamins such as vitamins C and E, the patient’s risk for heart disease
would be further reduced.81, 82
What’s more, the reduction or elimination of caffeine would also lower the patient’s risk for
coronary vasospasm and arrhythmia. And reducing coffee intake is an essential step in any program
to lower blood pressure and cholesterol. In fact, when nutrition, lifestyle, and caffeine reduction are
the treatment focus, research strongly suggests that medications are unnecessary.83, 84
Imagine the two choices before you. On the one hand, you modify your diet, learn (and practice)
a stress management technique, and add some nutritional supplements. You experience increased
feelings of well-being, greater stamina, some weight loss, a better sex life, and an improved health
report from your doctor on your next visit. Compare this to making no lifestyle or dietary changes
but taking prescription drugs every day. You keep the same habits to which you may be attached but
that compromised your health in the first place. You experience a variety of drug side effects such as
loss of libido and decreased energy, but that’s not the bad news. The bad news is the realization that
you’re going to have to take these drugs for the rest of your life, because without them, your blood
pressure and cholesterol will quickly rise to dangerous levels. Now, the question is, What kind of
health care do you want?
Caffeine and Gastrointestinal Health
WHAT’s YOUR GUT FEELING?
I was going to title this section “Gastrointestinal Disease” and discuss the various pathologies
connected with caffeine, such as ulcers and irritable bowel syndrome, but I realized that such an
approach would be far too narrow. It is critically important to remember that health is not simply the
absence of a specific, named disease. People whose gastrointestinal tracts (stomachs and intestines)
are inflamed and irritated are certainly not healthy, even though they may not be experiencing
enough pain and discomfort to send them to the doctor. People who self-medicate with antacids
every day are certainly not healthy, even though they may never be diagnosed with gastro-
esophageal reflux disease (GERD).
The wider and more accurate view of gastrointestinal health is one that looks at optimal function
and what compromises optimal function, not what destroys this remarkable tissue or necessitates the
use of drugs and surgery. In this context, you need to know more about the GI tract. I promise this
will not be boring or useless information. Rather, this “interior view” of your body might make you
think twice about the things you eat and drink, and have a dramatic effect on your health and
wellness.
THE HOLE IN THE DOUGHNUT
It’s important to understand that food, once swallowed, is still technically “outside” the body (much
like the hole is outside the doughnut) until it is digested and absorbed through the intestinal tract
into the bloodstream. The misconception is that this occurs easily, that by some automatic process
everything we eat is broken down and absorbed, and the remaining undigested fiber is simply
eliminated as waste.
In reality, the digestive process is neither easy nor automatic. It is an intricate and continuous
process, with numerous mechanical and chemical reactions taking place simultaneously.
Furthermore, each step of the process is dependent on previous steps, so a defect in one phase will
almost certainly hinder the entire process to some degree.
This critical function, by which we are nourished and thrive, deserves close attention. For the
health-conscious individual, that means learning what can be done to optimize digestion and what
habits and practices to avoid.
PERSPECTIVE
As I have mentioned previously, the genes that control every cell in your body haven’t changed even
a fraction of a percent in the last 25,000 years. That means your digestive tract is identical to that of
early Homo sapiens, designed, quite simply, for hunting and gathering. The idea that we should
postpone hunger satisfaction until a preset, time called lunch or dinner is, from a scientific point of
view, extremely bizarre, not to mention the fact that our meals today contain a mix of highly refined,
chemicalized foods, for which we are entirely unprepared, consumed in gargantuan quantities.
Medical anthropologists today are starting to understand that the changes in eating habits
brought about by the agricultural and industrial revolutions have placed an enormous burden on our
digestive systems. In short, our technology has outstripped our biology. Our genes have stayed the
same, while virtually everything about what and how we eat has changed completely. I believe this
is the principal reason why each year, over 30 million Americans suffer from acute or chronic
digestive dysfunction.85
Caffeine is one of those substances (along with refined sugar, “fake fats,” and hydrogenated
oils) that is completely foreign to the human gastrointestinal tract. Which is not to say that we can’t
detoxify the compound. Chapter 3 describes how your body accomplishes this arduous task. Rather,
it is the effects of caffeine that we need to explore and, believe it or not, we’re just beginning to get
a clear picture. One leading researcher has noted, “Despite more than a century of effort to elucidate
the actions of methylxanthines [primarily caffeine] in man, one of the major conclusions to be
drawn is that there is a need for further studies.”86 Here is what we know:
FUNCTIONS OF THE GASTROINTESTINAL TRACT
The GI tract has five major functions:
1. Microbial Defense: Throughout human history, most of the foods and beverages we
consumed were contaminated with bacteria and mold. The GI tract therefore contains a
highly specialized germicidal system comprised of hydrochloric acid (HCL) and a variety
of immune defenses, including secretory IgA (slgA).
2. Digestion: The complex starches, fats, and proteins we consume must be broken down
into simple units that can be absorbed into the bloodstream.
3. Essential Barrier:’the GI tract has the formidable task of keeping out any substance that
should not enter your bloodstream, including bacteria, food contaminants, allergy-causing
agents, and a variety of toxins produced during the process of digestion.
4. Absorption: Balanced against this barrier function, the GI tract must at the same time
facilitate the absorption of the substances you need. This requires precise conditions of acid
balance, enzyme activity, and timing.
5. Elimination: As an organ of elimination, the intestinal tract rids the body not only of
unusable food components, but also of a wide array of toxins and metabolic waste.
Each of these functions is critical to overall health and wellness, and caffeine alters or interferes
with all of them.
Caffeine Reduces Microbial Defense
There is evidence that caffeine interferes with the secretion and immune activity of secretory IgA,
and stress is once again the principal factor. As the stress hormone cortisol rises, slgA tends to fall.
This has been demonstrated even in mother’s milk.87 What’s more, the inverse relationship between
cortisol and slgA becomes more apparent when subjects are given a deep relaxation technique. As
stress hormone levels fall, slgA increases significantly.88 This gives us both new insight into the
value of relaxation and yet another reason to reduce caffeine intake. Optimal health cannot be
achieved with compromised immunity.
Coffee may also reduce the germicidal ability of the stomach, in what first appears to be a
paradoxical effect on HCL secretion. It has long been known that coffee (even decaf) is a strong
stimulator of HCL secretion.89 But that may not be the case when the beverage is taken with a meal.
Research shows, in fact, that caffeine consumed with food can actually decrease the normal and
necessary acid response to a meal.90 This reduces both the digestive and the decontamination
activity of your stomach.
Caffeine Impairs Digestion
Depending on when it is consumed in relation to food, coffee can either raise or lower production of
HCL by the stomach. If acid levels rise too far or too fast, one group of problems is created,
including increased risk for ulcer. If HCL secretion is reduced, food will tend to ferment and
putrefy, leading to the production of toxic by-products. Coffee has been found to produce a chain
reaction of maldigestion throughout the entire GI tract91—an especially important issue among the
elderly, as digestive efficiency tends to decrease with age.
What’s more, coffee may also speed gastric emptying, meaning that the contents of the stomach
are passed prematurely into the small intestine, cutting short the important gastric phase of the
digestive process.92
Caffeine Impairs the Barrier Mechanism of the GI Tract
If material from the stomach is released too early, it tends to be excessively acidic, and this may
injure sensitive intestinal tissue. Thermal or acid-related injury to this tissue is known to
compromise the barrier function of the gut, leading to the absorption of materials that you really
don’t want in your bloodstream.93
As you can imagine, this may set up a vicious cycle where reduced microbial defense combines
with impaired barrier production, leading to the absorption of toxins, bacteria, and allergy-causing
molecules. Colitis, for example, has been characterized as an intestinal “barrier dysfunction”
syndrome,94 and food allergy is directly related to the breakdown of the intestinal wall’s barrier
mechanism.95
Caffeine Impairs Nutrient Absorption
When you think about your GI tract, it is easy to understand the importance of absorption. After all,
that’s how the baked potato, broccoli, and filet of sole that you ate for dinner ultimately becomes
you.
I have presented ample evidence in Chapter 3 that caffeine reduces the absorption of a number
of vital nutrients. You may want to review that material, but let me simply list here the vitamins and
minerals that are known to be affected.
Thaimin and other B Vitamins
Calcium
Magnesium
Potassium
Iron
Zinc
Of course it is entirely possible that caffeine and coffee impair the absorption of other (or even
most) nutrients. It’s just that tests have not been conducted with the others. In animal experiments,
coffee and tea were both found to decrease the bioavailability of protein.96
Caffeine Disturbs Normal Elimination
Coffee is a frequent cause of both constipation and diarrhea, the effect differing from individual to
individual and also depending on when it is consumed. Coffee on an empty stomach causes
diarrhea, and this is a common experience.97
But caffeine can also cause constipation due to its diuretic action. In other words, caffeine tends
to pull water out of the digestive tract, leading to hard stools that are difficult to pass.98, 99
Now, of course, many people claim that caffeine helps them maintain normal bowel regularity,
but that is the same as relying on laxatives. Either way, you’re using a drug to induce bowel
movements, and ultimately many coffee drinkers become dependent on this laxative action.100
Without the caffeine stimulation, they experience what is known as “rebound constipation.”101
HEARTBURN
Of course it’s not the heart that’s burning, but the sensitive tissue of the esophagus. It’s burned by
acid regurgitated (refluxed) from the stomach, thus the medical term gastroesophageal reflux
disease, or GERD. The undeniable coffee connection has to do with the effect that coffee (even
decaf) has on the valve between the esophagus and the stomach.
For some reason, coffee reduces the pressure on this valve so that the highly acidic contents of
the stomach are allowed to pass up into the esophagus.102 Obviously, there are cofactors. Overeating
increases one’s risk to GERD, as does obesity, maldigestion, and lying down after eating. But the
coffee factor is quite significant, as demonstrated by the fact that you can stimulate heartburn in a
sizeable percent of perfectly healthy people just by giving them coffee.103
It was once thought that coffee-induced heartburn resulted from a hypersecretion of stomach
acid, but it appears that the coffee-induced valve defect is the primary cause. Heartburn sufferers, in
fact, have been found to produce less stomach acid when given coffee.104 I mention this in order to
point out the folly of treating coffee-induced heartburn with antacids. Notwithstanding drug
company hype, people don’t get heartburn due to an antacid deficiency. The prudent approach to
eliminating the problem (and not just masking the symptom) is to quit drinking coffee.
Of course, the coffee industry does its best to downplay the heartburn issue, and once again, the
reasoning is along the lines of, “If coffee caused heartburn, everybody would be suffering.” But the
truth is that, for unknown reasons, some people are just more sensitive than others. In addition,
certain types of coffee appear to create more severe symptoms.105
IRRITABLE BOWEL SYNDROME (IBS)
IBS is a common condition affecting approximately 20 percent of Americans.106 The complaints are
constipation (perhaps alternating with diarrhea), abdominal pain (dull or crampy), bloating,
abdominal rumbling, and flatulence. Now you might think with symptoms this common, researchers
would have discovered the cause, but, once again, the picture is only now coming into focus. Brand-
new evidence suggests strongly that there is a coffee connection involving two factors.
First is a group of rather caustic acids found in coffee. These acids, actually present at a higher
level in decaf coffee, can irritate the GI tract directly, causing cramps, discomfort, and diarrhea.
Second, there is GABA. Our last discussion of GABA (gamma amino butyric acid) focused on this
biochemical’s role in mind, mood, and behavior, and how it acts as a natural stress reducer in the
brain. “We now know that GABA is also produced in the gastrointestinal tract, for much the same
purpose.
The GI tract is essentially a tubular muscle with a variety of bulges, twists, and turns. Material is
moved from the stomach to the small intestine and on to the large intestine through a series of
rhythmic contractions known as peristalsis. Laxatives work by irritating the sensitive intestinal
tissue, which triggers accelerated contractions. Actually, anything that irritates the GI tract will tend
to have a laxative effect, and that includes anxiety. We all know the “gut-wrenching” feeling of
stress.
So nature placed in this system a large number of cells to manufacture GABA, as well as
receptors for GABA that would calm the GI tract.107–108, 109 From Chapter 4, we know that caffeine
interferes with GABA metabolism,110 and this explains why people with IBS experience a
worsening of symptoms when they drink coffee, as well as the widely variable effects of coffee
from person to person.
Scientists are now referring to the complex network of immune and nervous system cells within
the intestinal tract as the “brain of the gut.”111 Stress is perceived differently by different people, and
its effects throughout the body reflect this difference. What you must know is that coffee lowers the
stress threshold in your GI tract just as it does elsewhere in your body and mind. GABA is the
neurochemical that is supposed to keep your GI tract functioning at “normal,” and the combination
of stress and caffeine overrides that GABA message, creating the symptoms of IBS and possibly
much worse. Colitis has been positively linked to anxiety and stress,112 and animal research has
found that the GABA receptors are a first-line defense against colon cancer.113
THE ULCER STORY
You’ve probably heard that caffeine and stress don’t really cause ulcers, that the real cause is a
bacteria known as Helicobacter pylori (H. pylori). Here’s an intriguing fact: H. pylori is an
extremely common bacteria. Millions of Americans test positive for this organism, and by age
seventy,80 percent of the population has been infected, yet only 10 percent develop ulcers.114
Obviously, there must be other risk factors, and any investigation will quickly identify stress,
caffeine, and coffee. Coffee contributes to ulcer formation in a number of ways. The harsh acids are
a direct factor and, as mentioned, these acids are higher in decaf coffee. But caffeine itself is a
problem because it stimulates acid secretion in the stomach and interferes with the protective action
of GABA. In fact, coffee, tea, and soft drinks have all been shown to stimulate acid secretion,
especially when consumed on an empty stomach.115, 116
We also know that caffeine and chronic stress elevate blood levels of cortisol, which suppresses
a number of immune functions, including production of secretory IgA. As we have learned, slgA is
a powerful antimicrobial agent, especially effective against guess what? H. pylori!117 That means
that when IgA levels are low, H. pylori is allowed to proliferate and cause ulcers. When IgA levels
are high, H. pylori and other pathogens in the mouth, throat, and gastrointestinal tract are quickly
destroyed. When viewed in this way, H. pylori is actually a secondary risk factor. Stress, caffeine,
elevated cortisol, and suppressed IgA production are the primary factors contributing to ulcer risk.
Unfortunately, the modern drug-oriented approach to ulcers is simply a course of antibiotics and
acid inhibitors. They may help in the short run, but if nothing is done to reduce cortisol and restore
IgA production, the condition will recur. This is just one more example of “Band-Aid” health care
ignoring the underlying cause of disease. Consider that in research predicting the incidence of ulcers
in a large population, stress is the most significant factor.118 And in research evaluating the drug-
oriented approach to ulcer healing, the single most predictive factor for successful healing is the
patient’s anxiety level. In one study, those experiencing high levels of anxiety had a 400 percent
increased risk for incomplete healing compared to those with low stress.119
It’s an amazing but all-too-familiar scenario: Joe Executive goes to his doctor for his yearly
physical. Joe’s blood pressure is increasing, he’s not sleeping well, and he has lots of discomfort
after meals, and he uses antacids almost daily for the resulting heartburn. Caffeine is a known factor
in all of these conditions, but his doctor doesn’t even ask how much coffee Joe is drinking. There
are two reasons for this: (1) It would involve a discussion, and today the average office visit with a
primary care physician is twelve minutes and (2) the doctor is drinking four cups of coffee a day
himself. He or she hasn’t read the medical literature regarding caffeine and doesn’t believe it’s really
doing anyone harm.
Six months later, Joe returns. His intestinal pain has increased, and he reports sharp stomach
pain that gets slightly better when he eats. The doctor springs into action, writing prescriptions for a
drug that will prevent Joe’s stomach from producing digestive acid, and an antibiotic to kill H.
pylori. Joe leaves the office thinking that he has received health care. But the fact is that Joe’s
suffering was not caused by a deficiency of ranitidine, sucralfate, amoxicillin, omeprazole,
tetracycline, azithromycin, metronidazole, or any of the other drugs currently in use. All of these
medications have side effects, and there is even evidence that chronic suppression of acid secretion
can increase one’s risk for gastric cancer. (Remember that stomach acid is an important part of
gastrointestinal immunity.)
Please understand that I am not suggesting that one ignore an H. pylori infection. But evidence
clearly indicates that drug treatment alone is frequently ineffective, precisely because it does not
deal with the root problem. In fact, if dietary and lifestyle issues are not addressed, research shows
that reinfection can be as high as 73 percent.120 To get an idea of how shortsighted the drug-only
approach is, imagine that Joe went to a fortune-teller before his first physical:
Fortune-teller: “You are suffering from severe indigestion and heartburn.”
Joe: “That’s right, I am.”
Fortune-teller: “This is caused by stress, poor eating habits, and excessive coffee consumption.
But your doctor will overlook these factors. Instead he will wait for your symptoms to become
worse. In the meantime, a pathogenic bacteria will grow within your body and begin to eat away at
your insides. This will cause open wounds in the extremely sensitive tissue of your intestinal tract,
resulting in internal bleeding and acute pain. You will try to dull that pain with antacids, but it will
become so bad you will return to the doctor, who will give you drugs. The therapy will include
anywhere from two to four different drugs and the rate of success with this approach can be as low
as fifty-three percent.”121
Joe: “Wait a minute. That means I have nearly a fifty percent chance of not killing this
bacteria?”
Fortune-teller: “That’s right, and if the first course of drugs does not work, your doctor will try a
second treatment plan using more powerful drugs at a higher dose. Of course, it is almost a certainty
that the bacteria will have developed antibiotic resistance after the first course, so your chance of
success grows smaller with each additional trial.”
Joe: “Isn’t there anything I can do?”
Fortune-teller: “Sure there is. Stop drinking coffee, tea, and soft drinks. Eat slowly and chew
well. Eat smaller, more frequent meals, start an exercise program and make it a regular habit, learn a
stress management technique and take some time off, sign up for a yoga class and learn the
breathing exercises. Make sure to get at least eight hours of sleep a night, and slow down! Life’s too
short to suffer with internal bleeding from a perforated intestinal tract.”
A FINAL NOTE CONCERNING ULCERS
Coffee promoters have done a good job of whitewashing the ulcer issue, often relying on the
argument, “If coffee caused ulcers, everyone who drinks coffee would get one.” The fact of the
matter is that coffee doesn’t “cause” ulcers, but once again, there is a continuum of gastrointestinal
health with optimal function on one end, all the way to heartburn, irritable bowel, colitis, ulcers, and
colon and rectal cancer at the other extreme. Where are you now and where do you want to be? Do
you experience stomach or digestive problems more than a few times a month? If so, and if you are
a coffee drinker, you may be heading for trouble. Keep in mind also that when coffee is
administered to laboratory animals, in moderate but repeated doses similar to what humans
consume, it produces “pathological changes in the gastrointestinal tract and ultimately ulcer
formation.”122
OTHER GASTROINTESTINAL RISK FACTORS
Temperature
Most people drink their coffee piping hot, and the resulting increase in gastrointestinal temperature
has been shown to contribute to upper GI tract disorders.123
Food Allergy or Intolerance
Some individuals appear to be allergic to coffee (or possibly the chemicals it is treated with), and
this can increase the adverse effects associated with the beverage.124
The Melatonin Connection: Intriguing New Research
In Chapter 3, I described the critical role played by melatonin in regulating immunity and sleep. I
presented evidence that caffeine and coffee, especially when combined with other stressors,
significantly reduce melatonin levels.125
In addition to being a primary neurohormone produced by the brain, melatonin is manufactured
by a large number of cells in the gastrointestinal tract—another facet of the “brain of the gut.” And
melatonin’s effect on the GI tract is more than calming. Researchers believe that melatonin’s
principal role in the GI tract is to promote healing and boost immune defense. New studies show
that melatonin is particularly effect against stress-induced injury to the sensitive lining of the
intestinal tract and stomach.126 Not only is melatonin essential for the protection of this tissue, but it
has also been shown to enhance tissue DNA synthesis, indicating that it is also an agent for repair
and cancer prevention.127
We are finally understanding that the gastrointestinal tract is an incredibly complex and sensitive
environment. So much of our health depends upon maintaining the right balance of acids, enzymes,
and hormones. Moreover, this biochemical balance must be matched by the proper mechanical
function of valves, muscles, and organs.
When we eat natural foods (the foods this system was designed for) and consume these foods in
reasonable quantity at a reasonable pace, things tend to go quite well. But today’s diet presents a
level of digestive challenge unknown in human history. For eons, the only beverage humans
consumed was water. Today, Americans consume more soft drinks than any other liquid, and most
of that is caffeinated. What’s more, we consume coffee and tea in prodigious amounts, and then
wonder why we don’t feel well.
Of course, I’m not saying that everyone who drinks coffee is going to suffer with
gastrointestinal problems, but many people do, and they usually don’t make the connection. In
clinical practice, I saw hundreds of patients whose irritable bowel syndrome, colitis, food allergy,
gastritis, heartburn, bloating, and abdominal pain improved or healed completely once they got off
coffee. I concur with the advice given by Dr. Henry D. Janowitz, author of Good Food for Bad
Stomachs: “People with stomach ailments should avoid coffee and other caffeinated products.”128
Oh My Aching Back (and Wrist and Shoulders and …)
For years I had a practice in a comprehensive medical group that included physicians, chiropractors,
psychotherapists, and massage therapists. Usually I could tell by looking at a patient’s chart if he or
she needed to be referred to massage therapy. Experience told me that habitual caffeine users were
very likely to be holding enough tension in their muscles to cause a significant amount of
discomfort and pain. And I was right 95 percent of the time, even when pain was not one of the
patient’s listed complaints.
I am still amazed at the amount of pain that people become accustomed to living with. After a
while, we just sort of get used to it, assuming that it is an inevitable part of growing older.
Therapeutic massage, of course, brings pain and tension to the “surface” of our awareness, and often
prompts us finally to take steps to alleviate this suffering. Many, however, simply keep returning to
the massage table instead of eliminating the underlying cause.
The first step I recommend for someone experiencing chronic muscular tension is to get off
caffeine. Massage therapists, chiropractors, and physical therapists—anyone who works physically
with a patient’s body—can always tell a difference when the patient gets off caffeine. For many, that
step alone will reduce pain to a remarkable degree. Others need bodywork or yoga to release the
deep level of tension that we all tend to accumulate as we go through the trials and challenges of
life.
It helps to understand that tension is simply part of the stress response left over from Paleolithic
days when stress meant imminent peril. When faced with a fight-or-flight situation, tension helped
to steel the body against injury. But it’s no longer a survival asset. Tension today destroys our sense
of ease. It creates a level of pain that may flare up or smolder, but either way, it diminishes the
quality of life.
If you suffer from chronic pain and your physician has not recommended you stop drinking
caffeine, it’s probably because he or she has been told caffeine is a muscle relaxant. That is partly
true, in that certain muscles in the body do relax in response to caffeine, but these are only the
smooth muscles, such as those lining the airways. The vast majority of skeletal muscles contract in
response to caffeine, and those are the ones that ultimately produce tension-derived pain.
Very often, muscle tension combines with other factors, such as inflammation, to cause pain.
Such is the case with a common condition known as carpal tunnel syndrome (CTS) in which pain is
produced by a narrowing of the nerve channel in the wrist. CTS sufferers wear wrist splints, take
painkillers, often resort to surgery, and frequently none of those treatments is effective. That’s
because the underlying muscular tension must be reduced, and that won’t happen as long as the
individual is drinking caffeine.
In a study of nearly 1,500 office workers, caffeine use was found to be a primary risk factor for
CTS. In fact the correlation of caffeine use and this affliction held in both directions. In other words,
people who did not use caffeine had very low risk for CTS and those who used caffeine had the
highest risk. Since cigarette smoking is associated with caffeine use (and could confuse the issue),
the researchers removed from the data anyone who smoked. Even then, caffeine remained a primary
risk factor.129
Other research with chronic back pain illustrates the same association. In one study, individuals
with chronic back pain were found to be consuming an average of nearly 400 milligrams of caffeine
per day, while matched controls (people the same age and occupation without back pain) averaged
less than half that amount.130 Of course, this does not prove that caffeine causes the pain. It is
possible that pain sufferers turn to caffeine to help manage pain.
To clear up that possibility, researchers administered caffeine to volunteers and found that in
fact, caffeine produced head and neck pain in a significant percent of volunteers.131 This would tend
to confirm that caffeine is a contributing cause of pain syndromes from carpal tunnel to neck,
shoulder, and back pain.
THE CALCIUM CONNECTION
To understand just how caffeine produces muscle tension, you need to know that the drug disrupts
calcium ion flow through what are known as calcium-release channels. Smooth muscle lacks these
caffeine-sensitive calcium-release channels, so there is no contraction.132 Skeletal muscle, however,
is rich in calcium-release channels, and thus caffeine can cause contraction or spasm.133 In fact, the
sensitivity of muscle tissue to caffeine has been used by veterinarians to predict muscle damage
from strenuous running.
A procedure called the caffeine contracture test measures the degree to which a muscle contracts
in response to caffeine. Horses whose muscles contract severely in response to caffeine will be very
likely to incur damage from strenuous running.134 A syndrome of muscle pain after exertion has
also been identified in humans, and once again, the marker appears to be increased sensitivity to
caffeine.135
THE ULTIMATE TEST
Of course, the best way to evaluate the relationship of caffeine to your muscle pain is to get off the
drug and see how you feel. Many people have been amazed when an unlooked-for benefit from
quitting caffeine was relief from pain caused by neck, back, and shoulder tension. But remember, if
you’re suffering from chronic pain, going cold turkey off caffeine is likely to make your condition
worse before it gets better. Therefore I urge you to employ the Off the Bean strategy presented in
Chapter 10. That will minimize withdrawal symptoms and ease you into a different life—one in
which you are free of the background stress and tension created by caffeine.
Headache
Forty-five million Americans suffer from chronic headache. Seventeen million are migraine
sufferers. The relationship of caffeine to headache is confusing, not because the data is inconclusive,
but because for half a century, a major cause of headache has been promoted as the cure. Caffeine is
a common trigger for migraine and other types of headache.136 There is no mystery here. As we’ve
seen, caffeine increases tension in the jaw, shoulders, back, and neck. It has a powerful
vasoconstrictive effect in the brain. As little as 250 milligrams of caffeine has been shown to
decrease total brain cerebral blood flow by 30 percent.137 New research also shows that headache
sufferers commonly have low magnesium levels (measured as serum ionized magnesium),138 and
we have already learned that caffeine depletes the body of this essential mineral. Now consider the
following common scenario.
The person with a headache doesn’t know that it was caused or triggered by caffeine, so he or
she looks for a painkiller (analgesic). Studies show that in 95 percent of cases, the analgesic drug
contains caffeine.139 Such painkillers work, especially if the headache was caused by ****caffeine
withdrawal, but the caffeine ultimately triggers another headache. Ultimately, the hapless sufferer
becomes dependent on the painkiller for even a modicum of relief, but the headaches increase in
frequency and intensity. This may go on for many years, creating a cycle of pain and depression that
destroys the quality of life.140
And the cycle is not uncommon. Very often the patient’s doctor is the one to recommend a
caffeine analgesic. And often it is the same doctor who must ultimately admit the patient to a
hospital for analgesic abuse detox. The standard analgesic detox program looks like this:141
1. Withdrawal of caffeine-containing analgesics
2. Treatment of the withdrawal headache (which may last one to two weeks)
3. Therapy to reduce migraine triggers, including avoidance of caffeine
What’s wrong with this picture? Is it not crystal clear that if someone had told the headache sufferer
to avoid caffeine in the first place, a decade or more of pain and suffering, addiction, and depression
could have been avoided?
WITHDRAWAL AND BEYOND
A caffeine deprivation (withdrawal) headache results from the normal opening (dilation) of blood
vessels that are constricted by caffeine. In other words, habitual caffeine intake keeps blood vessels
in the brain constricted. When caffeine is not consumed, these blood vessels return to their normal
blood-flow potential, and it is this increased circulation in the brain that causes the throbbing agony
of caffeine withdrawal headache. In studies where caffeine is withheld or simply delayed, headaches
result from habitual ingestion of as little as 100 milligrams (one cup of coffee or two cola
beverages) per day.142, 143
Ultimately, of course, the brain becomes accustomed to normal blood flow and the headache
subsides. In Chapter 10, I will explain how to decrease or eliminate caffeine without suffering so
much as a single headache. But the point to keep in mind is that habitual caffeine users are
disrupting normal and essential blood flow to the brain. This is not a good thing, even if the body
does get used to such abuse.
And the caffeine-headache connection goes well beyond withdrawal. Caffeine itself contributes
to headache even when it is consumed moderately and consistently.144, 145 One landmark study
demonstrated significantly increased risk for headache at caffeine intakes of 250 milligrams per
day.146 Yet I continue to come across reports in the medical literature and popular press that caffeine
is a cure for headache. Perhaps the most bizarre is a recent article in the Medical Tribune advising
people who wake up with headaches to have a cup of coffee before they go to bed.147
Today, the most popular herb sold in America is Gink-go biloba. Ginkgo has been shown to
enhance peripheral blood flow, especially in the brain, and thus may be helpful in the prevention and
treatment of Alzheimer’s disease and some types of vascular disorders.148, 149 But clinicians are
starting to report that some people taking ginkgo are experiencing headaches. Do you see why?
Ginkgo dilates the same peripheral blood vessels in the brain that caffeine constricts. Thus habitual
caffeine users are taking ginkgo and giving themselves withdrawal headaches: the worst of both
worlds.
STUMBLING INTO ADDICTION
Here’s a classic example of how caffeine addiction and the commensurate headache can insidiously
sneak into a person’s life. At sixteen years of age, Caroline was attending a boarding school and
came down with mononucleosis. Sent home for a month to recover, she began drinking coffee for
the first time in her life simply as a way to cope with the profound fatigue.
Upon returning to school, where students were not allowed to drink coffee, Caroline began to
experience blinding, almost incapacitating headaches in the midafter-noon. She was given Excedrin,
two of which delivered a whopping 130 milligrams of caffeine to her 100-pound body. The
analgesic relieved her headache but also kept her awake until 3 A.M. As a result of disturbed sleep
and endocrine stress, full recovery from her illness, which is normally accomplished in four to six
weeks, took Caroline more than three years. What’s more, she became addicted to painkillers and
was not free of headaches until, as an adult, she eliminated all sources of caffeine in her diet.
>THE OPERATION WAS A SUCCESS, BUT THE PATIENT IS ADDICTED
Post-surgery headache has been noted in the medical literature for decades, and was until recently
attributed to a side effect of anesthesia. Then, a few years ago, someone made the observation that
people who abstain from caffeine do not experience such headaches. Ultimately, it was found that
the “postoperative headache” was in fact a caffeine withdrawal headache, since surgical patients are
not allowed to drink before their operation.150
Sensible solution: Get off caffeine. Preposterous solution: Put caffeine in the patient’s
intravenous drip. Action taken: The preposterous solution, of course!
I’m not making this up. It’s called prophylactic (preventive) intravenous administration of
caffeine, and it’s currently being recommended for habitual coffee drinkers who are undergoing
surgery.151
A New View on Caffeine Withdrawal
“Although the phenomenon of caffeine withdrawal has been described previously, the present
report documents that the incidence of caffeine withdrawal is higher (100 percent of subjects), the
daily dose level at which withdrawal occurs is lower (roughly equivalent to the amount of caffeine
in a single cup of strong brewed coffee or three cans of caffeinated soft drink), and the range of
symptoms experienced is broader (including headache, fatigue and other dysphoric mood changes,
muscle pain/stiffness, flu-like feelings, nausea/vomiting and craving for caffeine) than heretofore
recognized.”
Source: R. R. Griffiths, S. M. Evans, S. J. Heishman et al., “Low-dose Caffeine
Physical Dependence in Humans,” Journal of Pharmacology and Experimental
Therapeutics December 1990;255(3):l 123-32.
OXYGEN, THE ESSENCE OF LIFE
Whether or not you suffer from tension or migraine headaches, you have to ask yourself if you want
to con sume a drug (caffeine) that clamps down the blood vessels of your brain and restricts oxygen
delivery to billions of cells. In one more highly ironic twist of modern life, we now have oxygen
bars springing up around the country, supposedly to rejuvenate patrons with a superoxygen hit. But
many of these same people have just visited the espresso bar, where they loaded up on caffeine, thus
making the oxygen unavailable to their cells. Better to forget the oxygen, bar, stay off the caffeine,
and enjoy the natural vitality that exercise, adequate rest, and good diet can provide. I predict you’ll
have fewer headaches and more brain power to meet any challenge the day may bring.
Aging
You’re probably surprised to find aging in a section on health disorders. After all, every time the
earth circles the sun, we’re all one year older. But while that fact is inexorable, the consequences of
aging are neither inevitable nor immutable. We are learning that aging does not have to include
degeneration and decrepitude. It is possible, for example, to place two sixty-year-old women side by
side and have most people believe that one is the other’s daughter. Now mainstream medicine tends
to focus on the older-looking individual because mainstream medicine is concerned primarily with
the treatment of disease. On the other hand, I study the younger-looking one to see what can be
learned regarding prevention and anti-aging strategies.
Over the years, this line of inquiry has paid rich dividends as research uncovers significant
differences in the biochemical makeup of young- and old-looking individu als. We have discovered
differences in hormone levels and radically different levels of other important repair and rebuild
biochemicals such as insulin-like growth factor-1 (IGF-1). Much of that data was reported in my
book The DHEA Breakthrough (Ballantine, 1996), and while this is not the place for an exhaustive
review, there are critical points that need to be addressed in relation to coffee and caffeine. In
addition, new and extremely exciting data is being published every month that reveals the
importance of hormone production to longevity.
WHAT IS AGING ANYWAY?
There are a variety of theories that seek to explain the breakdown of human systems leading to
death. Over the years, they are either refined or disproved as more information becomes available.
When I was in graduate school, the genetic theory prevailed, that being the concept that “death
genes” (or perhaps, a single death gene) programmed tissues to self-destruct. But in more than
twenty-five years, such a gene has not been found. On the contrary, researchers have been able to
create conditions in which tissues live far longer than expected. The critical factors in aging appear
to be the efficiency by which nutrients are delivered, toxins are removed, and repair processes are
maintained.
Indispensable to all these life functions is water. Water is not only the environment within which
nutrient delivery, detox, and repair take place, it is an active and critically important participant in
every chemical reaction that takes place in your body. One of the primary markers of aging, of
course, is dehydration, and the loss of water from our tissues is accelerated by caffeine.152 That
means more lines and wrinkles on die outside, and a loss of metabolic efficiency on the inside.
Caffeine has significant diuretic effects even in habitual users. Even though considerable
attention has been placed on the nutrients that are lost in the urine, hardly anyone has looked at the
effects of the water loss itself. This is particularly ironic because coffee, tea, and soft drinks are
today more widely consumed than water, thus creating a vicious cycle of dehydration and diuresis.
What’s more, rehydration after exercise is actually impaired by drinking caffeinated beverages,153
and in yet another vicious cycle, dehydration appears to increase the toxicity of caffeine.154, 155
Therefore, the net effect of high caffeine use is accelerated aging, especially of the skin and kidneys.
CAFFEINE AND DETOXIFICATION
Detoxification, or die ability of the body to break down and eliminate toxins and waste, is a
biomarker of the aging process. We are used to thinking of the liver, kidneys, and skin as the major
organs responsible for this essential function, but each is entirely dependent upon water to get the
job done. Thus, any degree of dehydration can seriously impair the detox process, accelerate aging,
and increase risk to illness and disease.
While caffeine contributes to dehydration, perhaps the most important point to remember (from
Chapter 3) is that caffeine itself must be detoxified by the liver, and that is not an easy process. In
fact, high doses of caffeine may impair liver function, creating yet another metabolic stress. After
all, the liver is responsible for detoxifying not only caffeine, but the vast majority of foreign
materials that we are exposed to through water, air, food, and the environment. Most of these
substances, collectively termed xenobiotics, are broken down by a group of enzymes known as the
cytochrome P450 system (CP-450).
For years, scientists have used caffeine to evaluate stress on the CP-450 system. If a drug or
therapy is toxic to the liver, that organ will take longer to detoxify a given quantity of caffeine.156
The converse may well be true. Consider the liver function of an individual consuming large
amounts of caffeine. It stands to reason that the liver’s detoxification of other xenobiotics will be
impaired. Evidence in support of this theory comes from research with anticancer (chemotherapy)
drugs.
Remember that chemotherapy drugs are basically selective poisons that act chiefly upon rapidly
dividing cells, such as those in a tumor. One of the problems encountered by oncologists is that
these drugs become less effective over time. The body actually develops a tolerance or resistance to
the drugs because the liver gets really good at detoxifying them.
Caffeine, however, has been shown to reduce the development of such tolerance, presumably by
impairing the detox ability of the liver and inhibiting DNA repair.157 Now, lest you think this is a
good thing, consider the big picture. Caffeine is a drug that is consumed by millions of people, often
in amounts of 500 to 1,000 milligrams per day. If it is impairing the ability of the body to detoxify
xenobiotics, it is actually promoting disease (including certain types of cancer). The fact that it may
have some benefit in enhancing the effectiveness of chemotherapy drugs is hardly cause for
celebration.
HEREDITARY FACTORS IN DETOXIFICATION
In looking carefully at the CP-450 system, researchers have uncovered an extremely interesting
phenomenon. Some people, termed “slow acetylators,” have rather sluggish detox activity, and this
appears to be purely genetic. Slow acetylators will have impaired caffeine clearance, and their
detoxification of other drugs will also be impaired. Studies show that slow acetylators experience
more toxic effects after caffeine ingestion, and often have serious allergic-type reactions to a class of
antibiotic drugs known as sulfon-amides.158, 159
It’s important to understand that you have no way of knowing if you are a slow acetylator,
because such testing is not done on a routine basis. Research suggests, however, that the condition
may be extremely common. In one study, slow acetylator status was identified in 55 percent of the
control group population.160 Once again, this underscores the folly of blanket statements concerning
the safety of caffeine. Safe for whom? At what dose?
REPAIR
The ascending theory of aging at the moment is one of accumulated error. Scientists marvel at the
astounding ability of cells to repair and clone themselves, noting that our bodies are involved in a
massive twenty-four-hour-a-day regeneration process. But as cells continue to copy themselves, the
chance of error increases. Error, of course, results in the production of an abnormal cell, and when a
critical mass of abnormal cells is reached, the tissue malfunctions or dies, thus contributing to the
degeneration of aging.
The question, of course, is, “What causes the error? Theoretically, every cell’s DNA is a perfect
blueprint for the entire life, repair, and replication of that cell, and as long as the blueprint is
faithfully followed, error should not occur. But in biology, as in construction, mistakes happen. For
example, what if the blueprint is damaged?
Imagine a construction office where someone spills coffee on the blueprint. It’s quickly wiped
off, but a part of the document is smudged. Construction must continue, so the general contractor
guesses where the support beams are to be placed. As a result, eventually the building collapses.
Likewise, DNA can be damaged by an array of chemical and biological toxins. Collectively,
these are called mutagens because they cause mutation. Fortunately, your body also produces cells
that fix DNA. As you might have guessed, however, this DNA repair becomes less efficient as we
grow older, and caffeine appears to play a role in the decline. There are three aspects to this:
1. Caffeine is a known mutagen. That is, it can cause replication error, either by damaging
the DNA blue print or disrupting communication of that information to other “builder”
molecules like RNA.
2. Caffeine has been shown to inhibit DNA repairs.161, 162
3. Caffeine magnifies the DNA-damaging effects of other mutagens.163, 164
FREE RADICALS
Our bodies are also under assault by a group of metabolic and environmental toxins known as free
radicals. These dangerous biochemical “thugs” are unstable molecules or atoms that are produced as
a normal part of living. And under normal (or natural) circumstances, the body is able to control any
damage they do by the stabilizing activity of antioxidants. Vitamin C, vitamin E, and beta-carotene
are antioxidants that we obtain from food. Melatonin, glutathione, and superoxide dismutase are
antioxidants that are produced by the body.
But today, very little is natural. Most people’s consumption of antioxidant-rich fruits and
vegetables is woefully inadequate, and at the same time, free-radical exposure has skyrocketed.
Today, the pollution from industry and automobiles spans the globe and threatens the health and
welfare of everyone, primarily by free-radical damage. This vastly increased exposure can
overwhelm the body’s ability to stem the tide of cellular destruction. Massive levels of free radicals
are generated by cigarette smoke, auto exhaust, heavy metal and chemical pollution,
electromagnetic fields, ultraviolet radiation, injury, illness, and stress. The accelerated aging seen in
the deeply lined face of smokers is clear testimony to the damaging effects of free radicals.
GIVE ME A (COFFEE) BREAK
Recently, news that coffee contains antioxidants swept the nation.165 But in face, it only illustrated
how desperate we are for good news about coffee. As it turns out, it is the vapors of brewing coffee
that contain antioxidant elements, not the beverage itself. Even if you stick your nose next to your
coffeemaker and inhale deeply, you will not receive much antioxidant benefit from coffee. The
caffeine industry has also publicized studies that identify antioxidant properties of coffee, but these
are invariably conducted in test tubes, not the human body.166, 167
In fact, caffeine may very well potentiate free-radical damage in a number of ways:
1. Caffeine directly reduces tissue levels of melatonin, an antioxidant critical to the
protection of DNA.168, 169
2. In animal experiments, caffeine magnifies the free-radical damage produced by radiation
exposure.170
3. Caffeine raises stress hormone levels, which are known to accelerate free-radical
damage.171
AGE SLOWLY, NOT STRESSFULLY
The last point is probably the most important: Caffeine = Stress, and that dearly leads to
degeneration and aging, not vitality and youthfulness. Researchers have identified what is called the
stress-age syndrome, in which brain, endocrine, immune, and bioenergetic systems all start to fail
due to changes brought about by the ravages of stress.172–173, 174
Remember that caffeine and stress hormones also drive down levels of DHEA. As DHEA
declines, so does the production of important repair biochemicals such as growth hormone and
insulin-like growth factor-1 (IGF-1). In time, stress and caffeine contribute to adrenal exhaustion,
whereupon a raft of important hormones are depleted. This destruction is not silent. You’ll feel it
every day in many ways as you simply can no longer command the vitality necessary for what were
once everyday tasks
Finally, it is important to consider the role of disease in the aging process. It is obvious that
increased incidence of illness is both a cause and effect of aging. Thus, caffeine accelerates aging by
impairing immunity, something that has been shown to occur through the elevation of stress
hormones,175, 176 nutrient depletion,177, 178 and depression of DHEA.179 Look at common infectious
causes of death in the elderly such as influenza and pneumonia. It brings home the reality that we
are only as strong as our immune systems.
Caffeine and Diabetes (With a Note on Hypoglycemia)
A recent headline in the Medical Tribune announced DIABETES AT ALL-TIME HIGH IN U.S.180
The story unfolded nightmare-like, with experts expressing alarm and bewilderment as to the cause
or prevention of this epidemic. Since 1958, the number of Americans diagnosed with diabetes has
increased 600 percent, from 1.6 million to more than 10 million. What’s more, the Centers for
Disease Control estimates that another 6 million Americans currently have diabetes but are unaware
they have the disease.
These astronomical numbers do not begin to tell the story of suffering that diabetes brings. It is
a major cause of cardiovascular disease and commonly leads to kidney disease, blindness, chronic
infection, and foot and leg amputations. Nearly 20 percent of Americans over the age of sixty-five
have the disease.
“Diabetes is a common disease and becoming more common, and it is associated
with some horrible consequences.”
Source: Linda Geiss, Center for Disease Control and Prevention, Atlanta.
Like other health professionals and public health experts, I have watched this national tragedy with
growing concern. But here again, I part company with the mainstream medical community
regarding the appropriate response. Conventional medicine turns for help to the pharmaceutical
industry, which creates an ever-increasing number of drugs to manage diabetes. But this approach
seldom eliminates the destructive and often fatal consequences of diabetes. What’s more, these
drugs have a laundry list of potentially serious side effects that may create additional problems for
diabetics.
If diabetes were incurable, I would support drug treatment as a first-line approach, but the vast
majority of patients have Type II diabetes, which in most cases can be virtually eliminated with
nutrition and lifestyle modification. And one of those nutritional steps is the elimination of caffeine.
Here’s why:
1. Caffeine raises blood sugar levels and disrupts the blood sugar-regulating effect of
insulin.181 In fact, high-dose caffeine administration (the equivalent of six cups of coffee)
has been shown to produce transient insulin resistance that is very similar to Type II
diabetes.182
2. Caffeine raises fatty acid levels in the blood. Diabetics already have high blood-fat levels,
and the addition of caffeine can significantly increase their already high risk for heart
disease.183
3. Caffeine raises homocysteine levels, which greatly increases the diabetic’s risk for
cardiovascular disease and degeneration of blood vessels in the eyes.184, 185
4. Caffeine causes vascular resistance, in which blood vessels constrict and circulation is
reduced. Peripheral circulation is already impaired in diabetes, and the added effect of
caffeine can prove disastrous.
5. Caffeine raises stress hormone levels, a primary risk factor for diabetes. Exposure to
repeated stress increases the incidence of diabetes in rats.186 Chronic stress, including
feelings of irritability and hostility, has been linked to the development of insulin
resistance, leading to the diabetic state.187
DRAMATIC IMPROVEMENT AFTER QUITTING CAFFEINE
Shirley was one of those “hard to manage” diabetics. Wide swings in blood sugar made it almost
impossible to determine an effective dose of medication, and she suffered frequent bouts of
hypoglycemia, causing her to be hospitalized twice. At one point, her doctor suggested that she quit
drinking caffeine-containing beverages, but he mentioned it almost in passing and never explained
why he thought it was a good idea. Consequently, she made an effort to reduce her coffee
consumption, but she continued to have a large cup in the morning and another with lunch.
Then, at a support group meeting, a friend told her that quitting coffee altogether had helped
him tremendously. Figuring it was worth a try, Shirley started drinking a caffeine-free herbal coffee.
Within days, she noticed a leveling out of her blood sugar readings, and in two weeks, her blood
sugar dropped to the high-normal range. Encouraged by this breakthrough, she started an exercise
program and began watching her diet more carefully. Three months later, she was off medication
and had “cured” her diabetes.
AN OUNCE OF PREVENTION
For those with a tendency toward diabetes (and that includes anyone who is obese as well as lean
individuals with one or more diabetic parent), heavy coffee drinking can significantly increase risk.
The reduction or elimination of caffeine is an important preventive measure. Still, to this day, the
diabetes organizations have no recommendation regarding caffeine. Physicians are thus unaware of
the benefits of caffeine reduction, and patients are kept in the dark.
CAFFEINE AND JUVENILE ONSET DIABETES
Without going into technical genetic descriptions, let me simply say that juvenile onset diabetes is
similar to other hereditary diseases, in that the child inherits a susceptibility to the condition, not the
disease itself. For the past century, scientists have puzzled over exactly what triggers the overt
disease. Researchers in Finland and at the University of Pittsburgh believe they have found the
answer.
In a landmark paper published in the prestigious British Medical Journal, they provide solid
evidence that caffeine’s known toxic effects on fetal development include damage to the pancreatic
cells that produce insulin.188 By charting the incidence of insulin dependent diabetes against the per
person consumption of coffee in thirteen nations, these researchers illustrate a close correlation.
Critics, of course, will try to pass this off as mere coincidence, but the credibility of this type of
analysis improves according to the number of corresponding points. In this case, there is a tight
linear relationship for every country studied. Countries with the lowest coffee consumption have the
lowest incidence of diabetes mellitus, and countries with the highest coffee consumption have the
highest incidence of the disease.
HYPOGLYCEMIA
Hypoglycemia is often considered to be the “opposite” of diabetes. In reality, it simply refers to the
state of insufficient (hypo) blood sugar (glycemia) that may be part of or a prelude to diabetes.
In nondiabetic individuals, hypoglycemia may be caused by consumption of simple
carbohydrates, producing in an insulin surge that drives blood sugar levels below normal. Symptoms
include disorientation, depression, fatigue, confusion, and poor concentration; all resulting from a
shortage of glucose (fuel) to the brain.
Research has also confirmed that the hypoglycemic state can be induced and/or exacerbated by
caffeine. Investigators at the Yale School of Medicine Clinical Research Center documented the
following effects in human volunteers after ingestion of caffeine:
1. An immediate and sustained decrease of 23 percent in cerebral blood flow. This by itself
can produce feelings of confusion and disorientation.
2. Increased blood levels of stress hormones, epinephrine, norepinephrine, and cortisol
compared with placebo.
3. Marked symptoms of hypoglycemia even though the subject’s blood sugar was
considered low-normal.
The researchers concluded, “Our data suggest that individuals who ingest moderate amounts of
caffeine may develop hypoglycemic symptoms if plasma glucose levels fall into the ‘low-normal’
range, as might occur … after ingestion of a large carbohydrate load.”189
Commenting on the study, Dr. Richard Bernstein of Mamaroneck, New York, said, “Such an
effect could be dangerous. For example, if a person has low blood sugar and also drinks caffeine,
that person is more likely to be impaired.”190 And the lead researcher, Dr. David Kerr, noted that
“these symptoms may be greatest for children who drink caffeinated beverages.”191
The Adrenal Dysfunction Disorders: Allergy, Asthma, Fibromyalgia,
Chronic Fatigue Syndrome, and Autoimmune Disease
Your adrenals produce or contribute to the production of about 150 hormones, every one of which is
vitally important to health and wellness. Some of these hormones manage blood pressure; others
manage stress. And all this activity is accomplished by two glands smaller than your thumbs, sitting
on top of your kidneys.
In Chapters 3 and 4, 1 presented the scenario of adrenal stress resulting from the strains,
burdens, and anxieties of modern life combined with the biochemical stress of caffeine. I described
a “downward spiral” where the adrenals become exhausted and everyday problems then seem
magnified out of proportion. That’s because the adrenals are responsible for maintaining
homeostasis (metabolic and emotional balance) during times of stress. Once the adrenal buffer is
gone, you are constantly living on the edge of a breakdown. Your emotional resilience is reduced to
a continual effort to cope—plus you become a prime candidate for asthma, allergy, fibromyalgia,
chronic fatigue syndrome, and the autoimmune disorders discussed in this chapter.
Imagine if you had to live in a constant state of “emergency alert.” It would be exhausting. In
the same way, the adrenal glands, designed for episodes of stress (emergencies) in which
tremendous energy is needed to fight or run away, find themselves in a situation where heightened
activity is required all the time. And it’s not just job stress. It’s metabolic stress from poor food
choices, pollution, and electromagnetic radiation. It’s the pace of twentieth-century living and the
breakdown of family (tribal) support groups and community. And on top of that, most people add
caffeine, a drug that elevates stress hormones and can keep them elevated eighteen hours a day. For
the poor adrenals, there’s just no rest.
DELVING INTO ADRENAL FUNCTION
Until recently, no one bothered to look much at the adrenals. Even today, most doctors are only
aware of two tests to evaluate adrenal function. One test (for Addison’s disease) tells you if your
adrenals are completely shot. The other (for Cushing’s syndrome) tells you if your adrenals are in
hyperdrive, most often from an adrenal tumor. Between these two extremes, there is nothing your
doctor can tell you, other than that you appear “normal.”
All that is starting to change as researchers discover adrenal factors in a wide range of health
disorders. It turns out that the hormone balance maintained by the adrenal glands is much more
fragile than we thought. This section will discuss what I call the adrenal dysfunction disorders. As
you will see, adrenal weakness or adrenal insufficiency is the common factor that contributes to a
number of serious health disorders.
And now the effect of caffeine on the adrenals is finally coming to light. The caffeine
connection has been hidden by the fact that treatment for adrenal dysfunction disorders tends to be
shortsighted and one-dimensional. As I have explained before, understanding the health effects of
caffeine requires a long view, perhaps encompassing most of one’s lifetime. And from that long-
term view, a two-phase phenomenon is revealed.
PHASE 1: THE JOY RIDE
Phase 1 is what I call the honeymoon phase of caffeine consumption. This phase lays the
groundwork for long-term, caffeine-related damage to your mind and body. Ever-increasing levels
of stress hormones course through your veins, stressing your adrenals to the max. But for the
present, you actually experience some beneficial effects from caffeine consumption. Caffeine can
even seem like the answer to one or more of your health problems.
Here’s a good illustration. In the current caffeine mania that is sweeping America, even health-
food manufacturers and retailers have jumped on the bandwagon. Recently, articles have appeared
in health-food magazines talking about the benefits of organic coffee. Some articles have discussed
its mood-elevating effects, others imply that it is an aid to weight management, and a few even extol
the drink as a natural treatment for asthma.
Now all of these “benefits” are real, to some extent, but only in Phase 1. We have already
discussed how caffeine ultimately leads to depression. It’s weight-loss “value” is similar to that of
amphetamines, both in terms of temporary appetite suppression and ultimate side effects. And
asthma? Caffeine can indeed reduce the symptoms of asthma—temporarily. And then in Phase 2, it
makes them worse. That’s why the long view is so important.
First of all, you must remember why caffeine has these temporary beneficial effects. It’s all part
of the stress response, the ancient survival mechanism that enabled us to survive in times of
imminent danger. The increased respiratory efficiency that caffeine provides is purely a Phase 1
phenomenon; adrenal hormones are poured out to dilate the bronchial airways in order to send more
oxygen to the muscles. But does that make caffeine a sensible treatment for asthma? Read the next
section before you decide.
PHASE 2: PAYING THE PIPER
Habitual caffeine use ultimately leads to Phase 2, what has been called adrenal insufficiency or
adrenal exhaustion. This condition bears more than a casual resemblance to the post-traumatic stress
syndrome experienced by soldiers returning from combat. In effect, the adrenal glands simply wear
out from chronic stimulation.
Throughout this book, I’ve talked about the myriad effects of caffeine-induced excess stress
hormone production, from constricted arteries and elevated blood pressure to immune suppression
and stomach ulcers. But this is only half of the story. As caffeine intake continues and the adrenals
get weaker and weaker, a new set of problems arise that are related to stress hormone insufficiency.
That’s right—after a certain point, your adrenals are so exhausted that the pendulum swings the
other way. And that’s when you become most vulnerable to a whole new group of problems
associated with adrenal exhaustion: namely, disorders related to inflammation and autoimmunity,
among them allergy, asthma (inflammation of the bronchial airways), and even rheumatoid arthritis.
Consider this: We all know that adrenal hormones play a major role in the management of
inflammation. (For example, prednisone is a synthetic adrenal hormone that is used to reduce
inflammation in a wide variety of illnesses.) Adrenal hormones also help regulate the immune
system, preventing immune cells from attacking healthy tissues. Rheumatoid arthritis has both an
inflammatory and an immune system component. Recent research has shown that laboratory rats
bred to have insufficient adrenal hormone production develop rheumatoid arthritis far more
frequently than normal rats. It is also known that people with an adrenal disorder known as
Cushing’s disease are at high risk for depression, fatigue, and rheumatoid arthritis.
Recent research has found that abnormal adrenal hormone production in animals commonly
leads to mood disorders. Clinicians have long noted that patients with rheumatoid arthritis
frequently exhibit a type of depression characterized by fatigue, excessive sleep, and irritability. But
it was always thought that this condition was the result of chronic arthritis pain: Now researchers are
starting to think that the mood disorder and the inflammation may both be related to adrenal
insufficiency.192
The adrenal insufficiency model of autoimmune disease makes sense when you learn that the
onset of these disorders in humans is frequently associated with severe or chronic stress. Myasthenia
gravis, for example, is an autoimmune disorder characterized by progressive loss of muscle strength
and coordination. Current research suggests a strong adrenal stress component.193
THE DHEA CONNECTION
In Chapter 3, we learned that there is an inverse relationship in the body between stress hormones
(primarily cortisol) and the “vitality hormone,” DHEA, which is also .produced by the adrenal
glands. In Phase 1 of the caffeine/adrenal relationship, stress hormones are pumped out in excessive
amounts. This action suppresses immunity and increases risk for a number of health disorders,
especially cardiovascular disease. It also lowers production of DHEA, a hormone critical to the
optimum functioning of your immune, cardiovascular, reproductive, and nervous systems.
Ultimately, the resulting stress leads to Phase 2 and adrenal exhaustion. The decrease in stress
hormone production characteristic of Phase 2, however, does not result in increased DHEA. On the
contrary, the exhausted adrenals are unable to produce either sufficient DHEA or cortisol, and this
double whammy sets the stage for autoimmune disease. Men have a secondary supply of DHEA
from testicular production, while women do not, which may help explain why women report more
cases of autoimmune disease.
It is also interesting to note that a number of adrenal dysfunction disorders involve low levels of
insulin-like growth factor-1.194 IGF-1 is one of the body’s chief repair and rebuild biochemicals, and
its maintenance at optimal levels appears to be dependent on DHEA.
Until recently, however, very little attention was paid to the therapeutic benefits of DHEA.
Asthma, allergy, and autoimmune disorders were treated with synthetic adrenal (glucocorticoid)
hormones such as prednisone. And while these drugs certainly play an important role in the acute
stage of inflammation, the adverse side effects make long term use extremely unwise. Chronic use
of glucocorticoid drugs can cause weight gain, hypertension, seriously reduced immunity, emotional
disturbances, and bone mineral loss leading to osteoporosis.
DHEA may provide an alternative treatment. Researchers today are finding that, in at least one
autoimmune disorder known as lupus, treatment with DHEA produces significant improvement.195,
196 Most importantly, DHEA appears actually to help restore adrenal function.197
Once again, allergy is not an all-or-nothing phenomenon. The best way to visualize allergy-related
disease is on a continuum, from nonreactive all the way to a condition known as multiple chemical
sensitivity (MCS) (see figure below). MCS patients are sometimes unable to leave their homes
because even minimal exposure to outside air or pollution of any kind can trigger an allergic
reaction.
Your position on this continuum is very much related to the ability of your adrenal glands to
maintain adequate (but not excessive) levels of cortisol and epinephrine. Because caffeine and stress
weaken the adrenal response, they exert a pressure that, over time, pushes us farther and farther to
the right.
FIBROMYALGIA
Fibromyalgia is a chronic syndrome of pain that can range (and change) from tolerable to
incapacitating. While the pain is arthritis-like, fibromyalgia is not a type of arthritis. The pain, rather
than centering on the joints, is experienced more in muscles, tendons, and ligaments, and can shift
unpredictably. For the moment, fibromyalgia remains a mysterious disorder, diagnosed from a
symptom review and the existence of specific “tender points” on the body where even mild pressure
causes undue soreness.
Current research suggest multiple causative factors, and there is a very significant caffeine-
stress connection. New research has shown conclusively that patients with fibromyalgia suffer from
an adrenal weakness that includes insufficient cortisol secretion.206, 207 The pituitary hormone
signal that stimulates adrenal production of cortisol (ACTH) may be more than adequate, but the
adrenal response is still weak. Exercise, a positive stress that in a healthy person stimulates a rise in
cortisol, produces only a modest response in the fibromyalgia patient.208, 209 In effect, the syndrome
fits perfectly into the Phase 2 model described above.
The simple solution is to give fibromyalgia patients synthetic adrenal hormones, but as we have
already noted, the adverse side effects of these steroid medications are far too dangerous over the
long term. We are left, therefore, wondering how to restore adrenal function naturally. That topic
will be covered in Chapter 10. As you might have guessed, step one is to stop harming your adrenals
with caffeine.
In fact, there are four good reasons why anyone with fibromyalgia should avoid all sources of
caffeine.
1. Recovery is unlikely as long as your adrenals are stressed. Avoiding caffeine will greatly
increase your chance of recovery, a process that may take ten years or more.
2. The restoration of deep sleep is critical to the healing process. Sleep disturbance
(specifically reduced S-4 sleep) is one of the most common and long-lasting symptoms of
fibromyalgia.210 The medical term for this disturbance is “alpha intrusion of Stage 4
sleep.”
As we discussed in Chapter 3, deep (S-4) sleep is essential for repairing tissue damage.
Anyone with disturbed Stage 4 sleep will have aches and pains from unrepaired microtrauma
that occurs in the muscles and connective tissue. Whether from overexercise of a particular
muscle group, a new activity that involves use of different muscles, or simply an activity that
you haven’t done in a while (gardening in the spring), minor muscular injuries are common and
are normally repaired in deep sleep. In patients with fibromyalgia, these injuries appear to
accumulate211—and any caffeine intake only worsens S-4 sleep disturbance.
3. Caffeine causes anxiety, which is part of the vicious cycle of stress and fatigue. The net
result is that inflammation and pain are intensified.
4. Caffeine exacerbates other symptoms of fibromyalgia, including:
• Decreased circulation to the fingers and toes (known as Raynaud’s phenomenon)
• Tension headaches and migraine
• Irritable bowel
CHRONIC FATIGUE SYNDROME (CFS)
CFS is another multifactorial disorder with marked similarities to fibromyalgia. Many medical texts
group the two conditions together for diagnosis and treatment. In CFS, however, the most striking
feature is debilitating physical and mental fatigue.
What caught the attention of early researchers was the similarity of CFS symptoms to another
condition known as post-viral fatigue syndrome. But the search for a viral cause (such as Epstein-
Barr virus or EBV) turned out to be a dead end. EBV infection may play a role in chronic fatigue,
but the vast majority of American adults test positive for EBV and only a small percent have
chronic fatigue. There must be another factor that causes some individuals to fall apart in the face of
viral or other infection, and that factor may very well be adrenal dysfunction.
As in fibromyalgia, recent research confirms that chronic fatigue patients have low adrenal
function212 and low levels of cortisol, both at morning and evening time points.213, 214 The tie-in
with fibromyalgia is obvious, but researchers are now beginning to see that CFS may be part of the
wider picture of adrenal dysfunction215—in which caffeine intake is a major contributing factor.
I’m not saying that caffeine causes CFS or the other disorders we’ve discussed in this chapter.
However, one should not ignore the proven and well-understood damage that caffeine inflicts on the
adrenal glands and nervous system. It’s important to take the long view, and CFS patients should be
advised that using caffeine to get through the day will only prolong and deepen their debilitating
illness.
There’s yet another factor to consider. CFS patients have been found to have impaired clearance
of metabolic toxins, in itself a significant biochemical stress. These metabolic toxins result from the
normal metabolism of food, and they include bacteria, volatile fatty acids, amines, and bile acids.
Additional bowel toxins are produced by parasites and yeast organisms. It is the job of the intestinal
wall to prevent these substances from entering the bloodstream and surrounding tissues. In
“Caffeine and Gastrointestinal Health,” this chapter, I presented evidence that caffeine and coffee
both tend to impair the barrier function of the intestinal tract, leading to increased absorption of
toxic material into the body.
THE BOTTOM LINE
Anyone with allergy, asthma, fibromyalgia, chronic fatigue, or any other autoimmune disease will
tell you that their symptoms worsen or flare up when they’re under stress. In many cases, these
people can pinpoint exactly when their condition first appeared and relate it to a specific trauma or
stress in their life. If there is one essential lesson to be learned from this book, it is that stress is the
invisible saboteur of health and wellness. Conversely, anything that you can do to enhance your
experience of ease and peace will improve your life in myriad ways. The first step, as you know by
now, is to get off the bean.
Men’s Health
Earlier in this chapter, I presented a discussion of cardiovascular disease, by far the most significant
health risk for men related to caffeine. But as male baby boomers reach their fifth decade of life,
prostate health becomes a more and more pressing issue
The most common symptom of prostate dysfunction is abnormal growth of the prostate, which
then presses upon the urethra and causes problems with urination. Men with enlarged prostates
(known as benign prostate hypertrophy or BPH) have trouble voiding their bladder, so pressure
builds up and is difficult to release. Adding to the discomfort, this pressure also causes frequent
awakenings to urinate during the night. Most importantly, BPH is a risk factor for prostate cancer,
the second leading cause of cancer death in men.
As men age, the incidence of prostate infection and inflammation (prostatitis) also increases. All
of these maladies are treated with drugs. Some work by inhibiting the metabolism of testosterone,
some actually reduce testosterone production, and others fight underlying infection. Still, drug
treatments of BPH, prostatitis, and prostate cancer are not what you would call remarkably
successful. Surgery is being used more and more, and even the newest antibiotics often fail to
eradicate prostate infections. Moreover, surgery and drug therapies often have adverse side effects,
including decreased libido and impotence.
Thus, any man over forty is like to have a very uneasy feeling about his future health and
sexuality. By age seventy, more than 50 percent will have enlarged prostates, and by age eighty, the
number goes up to 80 percent. Here’s the good news: Men can significantly reduce their risk for
urinary and prostate problems by getting off coffee and caffeine. Milton Krisiloff, M.D., a urologist
in Santa Monica, California, was one of the first to notice that dietary modification, including the
elimination of all sources of caffeine, actually resolved prostatitis in the large majority of his
patients.216 In addition, he has clinical evidence that his simple program (the Krisiloff Diet) results
in decreased PSA scores for many men. High PSA (prostate specific antigen) is an indication of
increased risk for prostate cancer.217
Work by other investigators identifying an association between caffeine and urinary problems in
men supports these clinical observations,218, 219 and recently prostate cancer risk was found to be
directly linked to intake of theobromine, a methylxanthine related to caffeine. In that study, men
who consumed high levels of theobromine (commonly found in chocolate) had more than twice the
risk of prostate cancer compared to men who consumed very little of that substance.220
ISSUES OF MALE REPRODUCTIVE HEALTH
By now most everyone knows that sperm counts among men in Western nations are declining, and
the rate of decline is fairly alarming. A likely explanation for this is the increasing exposure to
pesticides and environmental pollutants, many of which are powerfully toxic to the reproductive
organs of men and women.221
As I have mentioned, coffee is the most heavily sprayed of all consumable commodities, but
residues in the final roasted product are reported to be quite low.222 Still, coffee and caffeine have to
be considered in any discussion of reproductive health for three reasons.
1. Beyond the directly toxic effects, pesticides, fungicides, and herbicides can have
cumulative effects on human health by altering hormone levels and hormone receptor sites
in the body. These endocrine modulating effects can be virtually invisible for decades,
producing symptoms only after many years of exposure. Thus, short-term research will
miss important long-term causative factors.
2. Clearly negative health consequences to animals are produced when they are fed caffeine,
and the ill effects are almost always centered on the nervous and reproductive systems.
Rats fed caffeine suffer testicular atrophy and low sperm counts as a result. Studies show,
in fact, that of all methylxanthines, caffeine has the highest reproductive toxicity.223 What’s
more, the amount of caffeine required to produce these adverse effects is not massive. One
study with rabbits found marked suppression of sperm formation at roughly the equivalent
of three mugs of coffee for a 150-pound man.224
Now, I know that you cannot equate rabbits and rats to human beings, but animal studies do
have relevance, especially when you consider that human beings with agricultural exposure to
pesticides exhibit precisely the same constellation of symptoms.225 And here’s one more
extremely intriguing observation: Men with agricultural exposure to pesticides who father
children have an astronomical prevalence of female offspring (83.4 percent versus the normal
of 48 percent).226 The same thing happens when male rodents are fed caffeine.227
3 A wide range of human subjects has been studied to evaluate sperm counts and sperm
motility. And whether you’re looking at men facing final exams, running a race, or simply
experiencing the stress of fertility testing, anxiety has a profound effect on sperm
quality.228–229, 230, 231, 232, 233 Motility (normal movement), sperm counts, and sperm
morphology (size and shape) all suffer when men are stressed, and, as we have well
established, one of the most reliable anxiety-producing influences in a man’s life is
caffeine.
PERHAPS MEN ARE NOT SO DIFFERENT AFTER ALL
We all want a healthy sex life for as long as possible. Men are often seen as being less willing than
women to alter dietary habits and incorporate new healthy lifestyle habits. But if something simple
like reducing caffeine consumption can keep us sexually vital and healthy, most men would choose
to alter their diet any day over the pain of disease and the possible adverse effects of medical
intervention.
The problem is that men often fail to recognize approaching danger until obvious symptoms
send them to their doctor. And doctors are more likely to write prescriptions than provide dietary
advice. So the issue becomes one of developing an increased sensitivity to the changes that occur in
our bodies as we age, including the urinary pressure and delay that signals early prostate problems.
Clearly, caffeine affects women’s reproductive capabilities, and we know that caffeine produces
stress that can affect male sperm quality. If you are a prospective father, it certainly seems prudent to
err on the side of caution and join your wife in eliminating caffeine from your diet.
GOUT. OH, MY ACHING FEET
Gout is a painful condition (considered a type of arthritis) that results from the deposition of uric
acid crystals in cartilage, the bones of the foot, and kidneys. For unknown reasons, gout is primarily
a male disorder, with only about 5 percent of patients being women.
There are a number of causes, mostly related to defects in uric acid metabolism, and these
defects appear to be primarily genetic. As is almost always the case, however, heredity only
predisposes one to the condition. Dietary and environmental factors play an important role. Diets
high in sugar and protein have been shown to elevate uric acid levels,234 as can caffeine.
The caffeine connection is demonstrated by a recent case in which the patient, a forty-eight-
year-old man, was “doing all the right things” to reduce his uric acid levels. He stopped drinking all
alcoholic beverages, adopted a vegetarian diet, avoided sugar, and maintained ideal body weight.
According to current medical knowledge, that was everything he could do. If he continued to
experience gouty pain, he would have to take drugs to lower his uric acid levels.
At his wife’s prompting, he stopped drinking coffee, and in a matter of weeks, his pain was
completely gone. That’s because one of the breakdown products of caffeine is methyluric acid, and
that can add to the body’s uric acid burden.235 In fact, allopurinol, the drug that is used to treat gout,
works by inhibiting the enzyme that converts methylxanthine (a caffeine metabolite) to methyl-uric
acid.236
Now, besides an inherited tendency to accumulate uric acid, liver disease significantly increases
the likelihood that caffeine will contribute to gout.237 If you remember that the liver is responsible
for the entire chain of breakdown steps in the detoxification of caffeine, this is not surprising. What
is surprising is that the elimination of caffeine is not (yet) a standard recommendation for
individuals with gout.
Caffeine and Your Eyes
Consider the astonishingly complex series of events that is taking place right now as you read this
book. The miracle of sight is an amazing process involving highly specialized cells held perfectly
within a fluid-filled sphere. Sight is the richest of our senses, accounting for about 75 percent of all
of our perceptions.
Often likened to a camera, the human eye is far more impressive. The “film,” for example, can
be used over and over again as long as the conditions are right for repair and regeneration. In fact,
the retina can capture more than ten images a second throughout life, sending information through
the optic nerve directly to the brain.
In fact, every structure of the eye is under constant repair, nourished by extremely fine blood
vessels and a fluid known as aqueous humor. The flow of aqueous humor maintains the internal or
intraocular pressure, and if this flow is impaired, pressure may increase, damaging the eye and
leading to a condition known as glaucoma. Glaucoma is a major cause of blindness, affecting
approximately 3 million Americans, and fully one-third of them don’t know they have the disease.
Caffeine significantly increases intraocular pressure in most people, especially when consumed
in amounts of four or more cups a day.238 If you have glaucoma, this pressure increase can occur at
half that amount.239 Experts believe that this results from changes in aqueous humor flow, and
studies have shown a remarkable difference in the fluid dynamics of the eye between volunteers
given caffeine and those given placebo.240
Perhaps even more serious (because it affects a greater number of people) is the decrease in
microcirculation in the eye caused by caffeine. Here again, as in the brain and peripheral blood
vessels, caffeine causes a marked constriction that limits the delivery of oxygen and vital nutrients
to these tissues. Animal experiments show that this can inhibit the growth and repair of the lens of
the eye.241 Studies with human volunteers illustrate that caffeine’s vasoconstrictive effect markedly
reduces circulation to the macula, the central portion of the retina.242 Macular degeneration is the
leading cause of vision loss and blind ness in people over sixty-five, with more than 16,000 new
cases reported annually in the United States.243 What’s more, evidence suggests that the incidence
of this condition is increasing rapidly.244
I find it remarkable that so little attention has been paid to the role of caffeine in eye health.
Caffeine’s diuretic effect can make your eyes so dry that wearing contact lenses is uncomfortable or
impossible. Caffeine contributes directly to the two leading causes of vision loss and blindness.
Today, health-food stores are filled with herbs, vitamins, and specialty products intended to decrease
risk for macular degeneration, cataracts, and glaucoma, and yet no one is sounding the alarm
regarding caffeine.
Antioxidants can help avert these common eye disorders by preventing free-radical damage to
the lens, retina, and macula. Ginkgo biloba and bilberry herb also help by improving
microcirculation. But none of these measures will have the best results if you continue to counter
their salutary effects with caffeine.
CHAPTER 6
Caffeine and Women’s Health
The hardest years in a woman’s life are those between ten and seventy.
—HELEN HAYES (at eighty-three)
You’ve Come a Long Way
Women today are under a tremendous amount of pressure to balance the demands of family and
career . Not that past generations of women had it easy—it’s simply that the pace of life, and
therefore the stress of life, has accelerated to the breaking point. What’s more, women are facing
these pressures alone, simply because the support systems of agrarian or tribal communities that
were common centuries ago have largely disappeared.
In this book, I have tried to get across the equation that Caffeine = Stress. This is a critically
important message, but it is opposed by powerful propaganda from the caffeine industry. Caffeine
products are advertised as a “pick-me-up,” with no mention of the fact that just a short time later
they become a “drag-me-down.”
It’s always a surprise to me when I suggest that a patient cut back on caffeine and she reacts as
though I’d asked her to betray her best friend. Even when I show her documented proof that caffeine
is contributing to many (if not most) of her health disorders, she finds it hard to believe that her
beloved coffee would do her harm.
With Friends Like These, Who Needs Enemies?
Let’s face it. We all grew up with the idea that coffee was something you shared in special moments
with a friend. This warm, fuzzy picture was conjured up by Madison Avenue ad men to get you
hooked on caffeine products. The advertisers know that if they can just get you to consume a few
cups of coffee or a few soft drinks a day, you will turn into a lifelong addict.
To illustrate how well this campaign has worked, one need only look at women’s health
literature. With very few exceptions, nothing is mentioned about eliminating caffeine, even though
the connection between caffeine and women’s health is undeniable and extremely important. In
Chapters 3, 4, and 5 we looked at caffeine’s contribution to a number of health disorders, including
heart disease, digestive problems, diabetes, fibromyalgia, panic attacks, depression, and anxiety.
This chapter will cover caffeine’s impact on issues specifically related to women, such as
premenstrual syndrome (PMS), menopause, fibrocystic breast disease, iron absorption, calcium
deficiency, osteoporosis, fertility and conception disorders, and complications of pregnancy and
childbirth.
The Gender Gap
When it comes to evaluating the potential dangers of caffeine, gender is the most important
consideration. Yet the entire issue is usually overlooked or ignored. Compared to men, research
shows that caffeine is much more damaging to women, producing adverse effects at lower intake.
The effects are even more far-reaching when you consider the harm caffeine does to fetuses and
nursing babies.
Given these facts, you may be surprised (and dismayed) to learn that roughly 75 percent of the
human research on caffeine has been conducted on men. Hopefully, this chapter will serve to offset
this astounding imbalance by describing exactly how caffeine affects women and what can be done
to minimize the health risks associated with caffeine intake.
First of all, women detoxify coffee much more slowly than men. What’s more, the half-life of
caffeine (the time it takes the body to eliminate one-half of a given dose) changes according to a
woman’s menstrual cycle. In the luteal phase (roughly the last two weeks leading to menstruation),
the half-life of a cup of coffee can be 7 hours, as compared to 5.5 hours in the follicular phase (the
first two weeks of a woman’s cycle).1 Moreover, a number of factors specific to women, such as the
use of birth control pills, reduce caffeine clearance even further. In fact, women on birth control pills
require about twice the normal time to detoxify caffeine.2
All of this means that the cumulative effect of daily caffeine intake is very significant for
women. A woman’s second (and even third) caffeine-containing beverage will hit her glands,
organs, and nervous system long before her body recovers from the first cup.
Caffeine just plain affects women differently than men, and it has to do with much more than
the decreased clearance rate. In one study, for example, men and women were given the same 150-
milligram dose of caffeine at the same time of day. The body temperature of the female subjects
increased, while the male subjects experienced a decrease in temperature. In addition, an hour after
caffeine administration, female subjects rated themselves as more sleepy, tired, and “disorganized”
than the male subjects did, and on standard cognitive tasks, the female subjects found that caffeine
made performance more difficult.3
Stress in general affects women more severely than men. Faced with threat or conflict, research
shows that women tend to have a much greater stress response compared to men, resulting in higher
blood levels of stress hormones.4 This response does not mean that women are “weaker.” On the
contrary, I believe it indicates that women tend to respond to conflict more seriously than their male
counterparts.
And they suffer for it. In one three-year study evaluating the effects of stress, elevated cortisol
not only increased risk for cardiovascular and other diseases, as it did in men, but in women the
stress response also predicted a decline in memory as well as cognitive and physical functioning.5
The Stress Chain Reaction
When the level of stress hormones (especially cortisol) is elevated, many of the body’s maintenance
and repair functions cease. How could it be otherwise? After all, this stress response was originally
intended to get us out of imminent danger. To mobilize all available energy for survival, Mother
Nature devised a way to shut down all noncritical functions in order to send blood, nutrients, and
oxygen to the heart and skeletal muscles.
As I mentioned in Chapter 4, few of us today ever face the kind of danger that requires
explosive action. Our stresses are the smoldering, chronic stress of twentieth-century living and
twentieth-century caffeine consumption. But even though the stresses are different, our bodies’
response is the same, and the shutdown of repair functions can weaken our bones, delay healing,
and create lines and wrinkles in our skin. In short, caffeine and stress accelerate the aging process.
Phillip Gold, a researcher at the National Institutes of Mental Health in Bethesda, Maryland,
compared the bone density of women with elevated cortisol to that of women with normal cortisol.
Although all the women were age forty, those with elevated stress hormones had the bone density of
seventy-year-olds.6
New Research Clarifies Heart Disease Risk
Remember how heart disease was once considered a “man’s disease”? For years, the vast majority
of research was conducted on men. Then someone noticed that just as many women die of heart
disease—however, for different reasons. Apparently, women are more likely to have fatal heart
attacks caused by coronary vasospasm, a constriction of the artery wall that shuts off blood flow to
the heart.
The likelihood of coronary vasospasm is related to both stress and caffeine. A study examining
the relationship between specific foods and the risk of heart attack in women found that the women
who consumed the most coffee had nearly three times the risk of heart attack compared to women
who drank the least amount of coffee. The association of caffeine and increased risk for heart attack
was stronger than the risk factor for total fat added to food!7
In the United States, breast cancer claims the lives of approximately 44,000 women
each year. At the same time, more than 235,000 are killed by heart disease.
Job Stress and Caffeine Linked to Depression and Hostility
Faced with overwhelming workloads from their families and their employers, women today are
falling apart in record numbers. Instead of being part of the solution, caffeine is very much part of
the problem. North Carolina researchers found that women who were overworked and experiencing
high levels of stress scored significantly higher on standard tests measuring depression, anxiety, and
hostility.8 In addition to the fact that such conditions are painful and reduce one’s quality of life, all
of these factors increase the risk for cardiovascular disease.
Other researchers from the University of California found that highly stressed female attorneys
who worked more than forty-five hours a week were three times more likely to have a miscarriage
during their first trimester of pregnancy, compared with those who worked less than thirty-five
hours a week.9 Again, caffeine, is a co-factor for two reasons: (1) People who work long hours have
been shown to drink more caffeine; and (2) conclusive research has found a significant association
between caffeine intake and miscarriage (see page 247).
Perhaps the new definition of “coffee break” should be “a break from coffee.” I encourage all of
my female clients (actually, I implore them) to replace the caffeine with herbal coffee, herb tea, or
another noncaffeinated beverage (see Appendix A, “Resources”).
Stress and Your Gastrointestinal Tract
It is well known that caffeine contributes significantly to anxiety, hostility, and depression. In turn,
these are powerful risk factors for irritable bowel syndrome and ulcers (see Chapter 5). “Women
with these characteristics [anxiety and hostility] were more than twice as likely to develop an ulcer,”
reports Dr. Susan Levenstein, who headed an eight-year study regarding psychosocial influences on
health.10 Women who were depressed at the start of the study were three times more likely to
develop an ulcer over the study period.
A Little Dose’ll Do Ya
Keep in mind that the damage done to the body and mind by caffeine is very much dose-related. A
little caffeine will do a little harm, while lots of caffeine will do lots of harm. Determining factors
include:
1. Your age, weight, overall health, and current medications. Remember that birth control
pills greatly reduce the liver’s ability to detoxify caffeine
2. Your sensitivity to caffeine. For unknown reasons, some people are simply more sensitive
to caffeine than others. This may be related to allergy, body type, adrenal health, or other
factors.
3. Your activity level after consuming caffeine. What do you do after you consume caffeine?
If you exercise, you can to some extent “work off” the stress hormones, glucose, and fatty
acids that were released into your bloodstream. But if you sit at a desk, the biochemical
events resulting from caffeine consumption will result in well-understood and documented
damage.
Caffeine Causes Serious Nutritional Deficiencies
Calcium deficiency, osteoporosis, and iron deficiency are three of the most common nutritional
problems in America today—especially among women. At the same time, coffee, tea, and soft
drinks are the beverages most often consumed with meals. It turns out that the relationship between
these nutritional problems and caffeine consumption is very well established.
Caffeine Facts for Women
FACT: Iron deficiency, inadequate calcium intake, osteoporosis, and depression are
devastating problems for women.
Fact: Caffeine dramatically reduces iron absorption.
Fact: Caffeine increases calcium loss and risk of osteoporosis.
Fact: Caffeine produces short-term mood elevation, but contributes to rebound depression.
Reduced Calcium Absorption
Over 65 percent of American women have low calcium intake, a condition that is aggravated by
caffeine’s ability to accelerate the loss of calcium through the urinary and intestinal tracts.
One recent study provides a smoking gun to implicate caffeine in calcium deficiency.
Researchers at Central Washington University investigated consumption levels of calcium and
caffeine in women thirty-one to seventy-eight years old. All women consumed approximately 200
milligrams of caffeine daily, “the equivalent of one to two cups of coffee.” This study showed that
total urine output of water, calcium, magnesium, sodium, and potassium increased significantly for
more than two hours following caffeine ingestion.11
Osteoporosis
Even with this conclusive evidence of caffeine-related mineral loss, health authorities hesitate to
affirm that caffeine is a risk factor for osteoporosis. That’s because the caffeine industry has created
a smokescreen around the issue, using studies that supposedly show that no danger exists. Let’s take
a closer look.
One study commonly cited by caffeine proponents is titled “Caffeine Does Not Affect the Rate
of Gain in Spine Bone in Young Women.” But if you read the study itself (and not just the title) you
will find that the subjects were college-aged women who consumed one cup of coffee per day. To
say the least, this level of caffeine intake is representative neither of college students nor of most
other American adults. Even the authors admit that the study does not in any way vindicate caffeine.
They state only that “one cup of coffee per day, or 103 mg, appears to be safe with respect to bone
health in this age group.”12 Surveys suggest that most American women consume that much
caffeine before noon.
Besides, if you’re trying to evaluate risk of osteoporosis, wouldn’t it be important to look at
postmenopausal women? Researchers at the University of California in San Francisco who did just
that found a significant association between caffeine consumption and reduced bone mass. In fact,
the caffeine—low bone density connection was found even in those women who took calcium
supplements.13
Another way to explore the issue is to study middle-aged but still premenopausal women. In this
category, leading researchers found that caffeine intake produced a double whammy on calcium
levels. The drug increased calcium lost in the urine and increased calcium loss through the intestinal
tract. Again, the amount of calcium lost was directly proportional to the amount of caffeine
consumed.14
For the skeptic who wants to see proof that such calcium loss results in greater risk for
osteoporosis, a very recent study conducted with women aged forty to fifty found that caffeine
intake was conclusively associated with decreased bone density,15 and research by the United States
Department of Agriculture confirms the findings. Results from the USDA study indicate that
women who consume less than the RDA for calcium (65 percent of all women in the United States)
face dramatic reductions of bone strength, especially when they consume more than two or three
servings of coffee per day.16
Another research strategy is to take habitual caffeine users and see what happens when they
stop. As expected, after only two weeks off caffeine, women showed significant improvements in
calcium status even while consuming a low-calcium diet.17
Still another perspective (if you need one) may be gained by looking at the association of
caffeine intake and hip fracture. Sure enough, data from studies covering nearly 90,000 U.S. women
show a positive correlation between caffeine intake and hip fracture. The largest of the studies found
that the risk for hip fracture for those who consumed the most caffeine was three times (300 percent)
greater than it was for the group that consumed little or no caffeine.18, 19
There are actually two contributing factors that weaken a caffeine user’s bones. We’ve discussed
the direct factor of increased calcium loss, but there are also indirect factors associated with the
increase in stress hormones. Caffeine raises cortisol levels, and with daily intake, that stress
hormone may remain elevated for long periods of time. We also know that caffeine contributes to
depression, and the combination of these two factors has telling effects. Women with a history of
depression, for example, have weaker bones compared to age-matched women without
depression.20 Again, this is due simply to the chronic elevation of stress hormones that is part of the
caffeine/depression scenario.
The goods news is that medical review articles are finally listing caffeine as a risk factor for
osteoporosis.21–22, 23, 24, 25, 26, 27 The bad news is that no one seems to be paying attention.
Material from the National Women’s Health Network states that the negative effect on bones from a
cup of caffeine is “more than adequately offset by a tablespoon or two of milk,” and the position
statement by the National Osteoporosis Foundation in Washington, D.C., states, “If calcium intakes
meet NOF standards, NOF considers caffeine intake in the range of 2–4 cups of coffee per day to be
without harmful effect on the skeleton.” I do not mean to denigrate these organizations, both of
which provide an extremely valuable service. It’s just that in regard to caffeine, they are, like almost
everyone else, unwilling to examine the evidence.
Caffeine, the Iron Robber
Not only does caffeine contribute to the loss of calcium, magnesium, zinc, and other valuable
minerals, but it also contributes to serious iron loss. The data is incontrovertible. A 1983 study
showed that one cup of coffee “reduced iron absorption from a hamburger meal by 39%.” The study
went on to state:
When a cup of drip coffee or instant coffee was ingested with a meal … absorption was
reduced from 5.88% to 1.64% and 0.97% respectively, and when the strength of the instant
coffee was doubled, percentage iron absorption fell to 0.53% … The same degree of
inhibition as with simultaneous ingestion was seen when coffee was taken 1 hour later.28
I must explain the consequences of this astounding finding. Most women spend their entire lives
malnourished in iron, and nearly 30 percent will be frankly anemic until they stop menstruating.
This is because it is very difficult to absorb iron from food, and unless a woman has a great diet and
perfect digestion, her monthly blood loss will tend to exceed her absorption of this essential
mineral.29 Add caffeine to that equation and the likelihood of insufficient iron approaches certainty.
Depending on the composition of a meal, a caffeinated beverage can reduce iron availability by a
whopping 50 percent.
What’s more, caffeine impairs the absorption of any iron supplement taken to correct the
deficiency. Documented cases have appeared in the medical literature showing that anemia
wasincurable until the patient stopped consuming caffeine.30
”Considering the high incidence of iron deficiency anemia worldwide and its likely
association with immune function and mental development, these findings indicate
that dietary habits such as coffee and tea consumption deserve as more attention
potential causative factors.”
Source: American Journal of Clinical Nutrition, 1988;vol. 48:645–51.
As you might know, the statistics on iron deficiency are alarming. Research shows that iron
deficiency is the most common nutritional deficiency in the United States, Canada, Australia, and
western Europe.31 But what exactly does that mean? We’re used to hearing about “iron-poor blood”
causing a certain lack of zip and energy, but iron deficiency is much more than that. In fact, there
are three distinct levels of iron deficiency, and I’ll bet you’ve heard only about one. Don’t feel bad.
Your doctor may not know any more about this important issue than you do.
Anemia as a Measure of Iron Sufficiency… and Other Myths
Imagine that you had a financial adviser to manage your estate. One day, he calls you and announces
that you will have to file bankruptcy because you are broke. “What?” you exclaim. “How is that
possible? When you started managing my account, I had two million dollars!” “Well,” he says,
“about three years ago, I put all of your money in a gold-mining operation. Over the years, it has
done quite poorly.” “Why didn’t you tell me I was losing enormous sums of money for three years?”
you ask. To which he replies, “Well, technically speaking, you weren’t completely broke, so as long
as you had some money, I didn’t think of bringing it up.”
If this scenario sounds absurd and unbelievable, you have to understand that most doctors have
followed this approach for decades with their female patients in regard to the precious commodity
known as iron. That’s because doctors have been looking only at the woman’s complete blood count
(CBC). If she’s anemic (bankrupt), they tell her. If she’s not anemic, they let it slide. The fact of the
matter is that a woman will typically be iron deficient for two to three years before she becomes
anemic.32 At that point, anemia is difficult to cure. But if iron deficiency is identified in its early
stages, it can easily be treated and anemia avoided.
Shocked reader: “It must be that there is no reliable way of determining the early stages of iron
deficiency. “ Ah, but there is. It’s a simple and inexpensive blood test that measures body stores of
iron, called serum ferritin.
Shocked reader: “But my doctor does measure serum iron, and he always told me it was
normal.” Serum iron is a meaningless test. It only tells you how much iron is traveling through your
blood. You can be frankly anemic—hardly able to get out of bed—and have normal serum iron.
Shocked reader: “Gosh, this serum ferritin must be a new test.” Actually, the test has been
available for nearly thirty years. Studies confirming its value as the definitive test for iron status
were published in 1979, and verified repeatedly for the past two decades.33–34, 35, 36, 37 By now, the
consensus among experts is that the only accurate way to determine iron nutriture is by evaluating
ferritin and other iron parameters. What’s more, serum ferritin is also the only iron indicator that is
able to differentiate between true iron deficiency and anemia due to infection.38
Shocked reader: “If this is such a critical issue, why in the world has it not been diligently
pursued?” Well, iron deficiency is primarily a problem for women, and most physicians and
researchers are men. Additionally, the cure for the problem is a nutritional supplement and not a
prescription drug, so the issue doesn’t get much attention. There is, however, a growing body of
research showing that ferritin is a critically important factor in evaluating (and even preventing)
atherosclerosis,39 so we may yet see the test performed routinely.
The take-home message here is that there is a progression of iron deficiency. You’re not
optimally nourished in iron one day and anemic the next. It’s important to have a sensitive marker
for iron status because there are clear symptoms way before the anemic state. Most symptoms are
related to energy and mental alertness, so the connection with caffeine is more than casual.
For example, a woman with low iron stores is likely to have low energy and a hard time
concentrating. Chances are she will also be depressed. And since she doesn’t know these conditions
are related to malnutrition, she will most likely chalk it up to growing older or her personality.
What’s more, she will probably resort to using caffeine in order to cope with these feelings, and that
brings us to the next vicious cycle:
of calcium in the American diet. The scenario gets even worse when you
remember that caffeine also tends to increase calcium loss in the urine.
The effect of caffeine on children’s growth is nearly impossible to evaluate
because it would be unethical to dose children with caffeine in order to measure
changes in growth rate. But in some South American cultures children drink a
significant amount of coffee. One recent study in Guatemala found that taking
children off caffeine for just five months resulted in 22 percent gains in length
compared to the group that continued drinking coffee. More important, the
caffeine-free group registered a 46 percent greater weight gain and decreased
incidence of illness.30
The caffeine habit is a terrible legacy to give our children. During
adolescence, there is a window of opportunity to form strong bones, and those
bones must last a lifetime. Once a child’s skeleton is fully formed, very little can
be done to increase its mineral content. And at this all-important moment when
every gram of calcium and magnesium count toward either future health or the
pain and crippling of osteoporosis, we hand our kids a can of pop.
RESEARCH CAPSULE
What’s Wrong with This Picture?
In the April 1, 1996, issue of Family Practice News, I was surprised
to see an article titled “Carbonated Beverages No Threat to
Bones.”31 Numerous studies show an undeniable association
between high soft drink consumption and increased risk for bone
fractures. Was the present study really debunking the cola
connection? You be the judge.
Point 1. The chief researcher announced that five colas have “about
the same amount of caffeine as one strong cup of coffee.” In fact, a
twelve-ounce cola contains 45 to 72 milligrams of caffeine, so five
soft drinks will deliver at least 225 milligrams and as much as 360
milligrams of caffeine. A strong cup of coffee contains 120
milligrams of caffeine per six ounces.
Point 2. The mean age of the women in the study was seventy-two.
Point 3. Soft drink intake was determined by lifetime recall, a
technique notorious for error.
Point 4. The average soft drink intake of the women in the study
was one serving per day.
Conclusion: This study proves only that elderly women who
remember drinking approximately one soft drink per day do not
have weaker bones than elderly women who remember drinking
less than one soft drink per day. It never tested the real question as
to whether soft drinks in amounts commonly consumed today
contribute to bone loss or fracture. Nevertheless, this study became
a news item, reducing concern regarding the soft drink-osteoporosis
connection.
The Truth: A careful review of the effects of soft drinks on bone health was
recently conducted and published in the journal American Family Physician. The
researchers conclude that “excessive consumption of carbonated and cola-type
beverages, combined with low dietary calcium intake, is a major public health
issue that predisposes female adolescents to bone fracture and perhaps increases
the likelihood of osteoporosis later in life.”32
Soft Drinks Promote Hypertension
It has long been known that decreased intake of calcium and magnesium directly
and significantly increases the risk for hypertension in adulthood. But recent
research with children shows that suboptimal intake of these important minerals
is also associated with something that was unheard of a generation ago: pediatric
hypertension.33 Once again, by foisting soft drinks upon our children, we are
setting them up for a serious lifelong disorder. That’s because caffeinated soft
drinks:
1. Provide no calcium or magnesium;
2. Replace other nutritious beverages that normally provide these
important minerals;
3. Actually deplete calcium and magnesium from their bodies; and
4. Contribute directly to hypertension.
Soft Drinks Have Invaded Our Schools
Many studies show widespread suboptimal nutriture in American
schoolchildren.34 How did this happen? Amazingly enough, a large part of the
answer lies in our schools.
More than thirty years ago, when soft drink consumption was nothing
compared to what it is today, the Council on Foods and Nutrition of the American
Medical Association issued a statement expressing its strong opposition to the
sale of carbonated beverages in school lunchrooms.35 Then, in the 1970s,
carbonated beverages were allowed to be sold, but only after the lunch period had
ended.
In 1983, soft drinks were prohibited only during the actual service of food, the
rationale being that the U.S. Department of Agriculture considered such
beverages to be inappropriate in nutrition education settings. But today there are
soft drink machines in high schools across America, and average teen
consumption is pushing three cans a day. Here’s how it happened.
Imagine you’re a school administrator and budget cuts have forced the
cancellation of your junior varsity sports program. Then you receive a visit from
a cola company representative, who expresses concern that you are under such
tight financial constraints and suggests a solution. If you authorize the placement
of cola vending machines throughout your campus and sign a contract granting
exclusive sales rights (for about ten years), the cola company will pay a
commission on each can sold—and, in time, you’ll get your sports programs
back. Suddenly, cola machines appear all over the school—in the lounges,
cafeteria, and, in some cases, the hallways.
An article on this subject in The New York Times on March 9, 1998, quoted
Larry Jabbonsky, a spokesman for Pepsi-Cola, as saying, “They [the schools]
need to generate funds. At the same time, we are constantly looking for new ways
to broaden our exposure among young people. It’s a pretty natural independent
fit.”36 Though neither Coca-Cola nor Pepsi (the two biggest players) will say how
many schools have signed deals, this movement is exploding across the nation. In
November 1997, the Colorado Springs, Colorado, school district signed a ten-
year deal with Coca-Cola for $8 million, and more if it exceeds the “requirement”
of selling 70,000 cases of Coke products annually.37
“While soft drink giants have long fought to be designated the
official beverage of professional sports and college campuses, only
recently have they turned their sights on the kindergarten-through-
high-school set.”
Source: The New York Times, March 10, 1998, page Cl
Money from the cola companies is funding not only sports programs, but new
computer programs and more. The schools are delighted with the easy money and
apparently have no issue with treating the students as a commodity to sell to the
highest bidder. Meanwhile, the issue of our children’s health has fallen
completely by the wayside. In The New York Times article quoted above, health
issues surrounding soft drinks were not even mentioned. Consumers Union
decries the practice of soft drink deals, not because of the health hazards, but
because it is “using taxpayer space to promote commercial messages and give
over these audiences to corporations.”38
While school administrators and cola executives are congratulating
themselves on a win-win deal, the real losers are the children. They lose critically
essential nutrients at a time when every vitamin and mineral counts toward a life
of health or illness. They lose the freedom to choose what beverages they want to
consume, and they lose an environment that encourages free thinking, as schools
plaster contract-mandated advertising on the buildings, scoreboards, cups,
banners, and vending machines. One Texas school district has cola brand logos
painted across the rooftops of its two high schools. And, of course, the kids lose a
measure of self-determination as they become addicted to caffeine.
“You want to get them started young and hopefully keep them for
life—that’s what brand loyalty is all about.”
Source: Ira Mayer, publisher of Youth Markets Alert.
Of course, universities have been signing exclusive soft drink deals for years, and
they’re proud to point out that much of the cola money goes to fund women’s
athletic scholarships.39 The irony is that caffeine increases a woman’s risk for
anemia, PMS, osteoporosis, fibrocystic disease, anxiety, and depression (see
Chapter 6), making cola beverages the very antithesis of peak sports
performance.
And It’s Not Just the Schools
Even as more children every day become casualties of the cola wars, soft drink
manufacturers are going out of their way to promote their products through youth
service and educational organizations. Some point out that these deals usually
involve significant donations, but does that justify promoting products that harm
children?
The New York Times recently reported that the Boys and Girls Clubs of
America and the Coca-Cola Company would jointly raise $60 million over the
next decade for a youth development program sponsored by the clubs.40 Seems
like the cola giants are only too willing to lend a helping hand to our kids, all the
while creating a whole new generation that will grow up addicted to caffeine.
And Just When You Thought It Couldn’t Get Any Worse…
Soft drink manufacturers today are rushing to bring products to market with
greatly increased caffeine levels—as much as 168 milligrams per twelve-ounce
serving! In 1996, Pepsi brought out Josta, which combines two sources of
caffeine, and Coca-Cola quickly responded with their own supercharged brand
called Surge. As this book was going to press, more than a dozen companies were
jumping on the high-caffeine bandwagon with product names like Guts, XTC,
Krank, Jolt, Power Kid, Boost, and Zapped. Once again, the trend is being fueled
by an illusion, created by manufacturers, that such products provide energy. In
fact, the caffeine in these beverages produces nothing more than metabolic,
biochemical, and emotional stress.
School administrators are witnessing this firsthand as manufacturers fill
school vending machines with high-caffeine products. In a recent New York Times
article, Margaret Mohrman, headmistress of the Academy, a school for gifted
students in Little Rock, Arkansas, explained that the school banned Surge from
its snack bar after students drank themselves into a caffeine frenzy. “I just
couldn’t believe it,” she said. “The kids were holding two in their hands and
drinking one after another. When they weren’t jumping up in the bathroom, they
were climbing the walls.”41
For parents, these high-caffeine products present a real dilemma because they
are sold in schools and convenience stores everywhere, and kids are under
tremendous pressure to “get their kicks” from a can. Indeed, the manufacturers’
trademarked slogans are all geared toward a drug-oriented “high” with caffeine as
the drug of choice. Below are a few examples:
Beverage Slogan
Jolt “America’s most powerful cola.”
Krank 20 “Water with caffeine, lots of cafferine.“
XTC “ A Carbonated slap in the face”
Sugar ”Feed of rush.“
Go Go ” It’ll blow your mind.“
Josta “ Unleash it.”
The point that needs to be remembered is that these products are not only being
marketed to teens and the twenty-something age group. In fact, sales are geared
to children as young as seven, using cartoon characters as enticements. The New
York Times reports, “Market research shows that Mountain Dew [the original
high-caffeine soda] is more than twice as popular as other soft drinks among
children younger than 6.”42
There is no doubt that the “rush” induced by these products is harmful to
children. Caffeine affects their brains and growing bodies in ways that have never
been evaluated because no one would dare administer high amounts of caffeine to
a child in a controlled study. Tragically, there is no safety data, and the marketing
campaigns that flood the airwaves are reprehensible in light of caffeine’s well-
known negative effects on the body and mind.
The Relentless Push Continues
Recently, cola companies hit upon yet another strategy to increase consumption.
In case you haven’t noticed, twelve-ounce cans are gradually being replaced with
twenty-ounce bottles, thus increasing the serving size by 65 percent. These
twenty-ounce bottles deliver an astounding fourteen teaspoons of sugar and
enough caffeine—seventy-five milligrams—to produce quick addiction and
severe withdrawal.
Clearly, caffeine is a drug being administered as a food. No scientist or health
professional would deny this. Yet the only guidance that the public receives
regarding soft drinks is to consume them “in moderation.” At the same time, the
soft drink industry has made every effort to thwart even this modest goal. They
refuse to put warning labels on their products, refuse to disclose the amount of
caffeine in their products, and then create products with ever higher levels of
caffeine in ever larger servings.
To make matters worse, the FDA has literally stood by and watched the
drugging of America take place. Their inaction has led many people to assume
that caffeine is harmless and perfectly fine for children. Now that the truth is
known, the question is: What shall we do?
I believe that the pendulum is about to swing. The proliferation of high-
caffeine beverages is already having a serious effect on the nation’s health, and it
is only a matter of time before people start to take action. From my point of view,
we need to begin with efforts to protect our children. For starters, I believe that
soft drink machines have no place in schools, that soft drinks should list their
caffeine content, and that people should be educated concerning the real and
significant consequences of caffeine addiction. Only then will we be able to
consume soft drinks “in moderation,” or not at all.
CHAPTER 9
Options and Alternatives
If your life revolves around caffeine, be it in a coffeepot,
teacup, or soda can, don’t despair. The purpose of this book is
not just to give you the bad news about caffeine. The good
news is that there are plenty of delicious, caffeine-free
beverages that will enrich your life and at the same time
support optimal health. Fortunately, we live in a time when our
global society offers us an unprecedented choice of foods and
beverages from all over the world. After reading this chapter,
you will be fully informed about a wide selection of alternative
beverages to taste and explore.
Developing new lifestyle habits takes experimentation and
time. Importantly, your taste buds will readjust as you make
changes in your diet. Beverages that were once strange and
unfamiliar will become more satisfying and delicious than
your old caffeinated beverages. You’ll feel better physically,
and life will hold more possibilities. If “variety is the spice of
life,” then read on to discover the diversity of beverages that
can help you successfully reduce or eliminate your caffeine
intake.
Decaf versus No-caf
Many of you who are coffee drinkers might be thinking, Why
don’t I just switch to drinking decaffeinated? First, you have to
remember that decaf doesn’t mean no-caf. Decaf coffee beans
have undergone an extraction process to remove the majority
of the caffeine, but there is still some left. A twelve-ounce cup
of decaf typically contains at least 10 milligrams of caffeine,
and possibly more depending on how it’s brewed.
Second, you have to look at your own health reasons for
reducing or eliminating caffeine. For example, if your liver
can’t properly detoxify caffeine or your adrenals are
completely exhausted, 10 milligrams multiplied by several
cups per day may still aggravate your condition. If your body
reacts to coffee with allergic responses such as skin rashes or
mood swings, or if you suffer from any of the problems listed
in Chapter 5, even decaf coffee may be a problem.
DECAF AND YOUR STOMACH
The acidity of coffee is higher in decaf because robusta beans
are commonly used to produce decaf coffee. Robusta beans
have a higher caffeine content and a stronger acidity than
arabica beans, so more of the coffee flavor survives the
extraction process. But the acids and oils that carry the flavor
can be harsh on the intestinal tract and are often a problem for
sensitive individuals.
If you suffer from digestive and gastrointestinal
disturbances (especially ulcers), eliminating coffee altogether
is the healthiest choice for you. Coffee often causes a hyper-
secretion of stomach acid, which is why many people have to
eat something with their coffee or suffer from acid indigestion.
$$$ Moreover, decaf still frequently causes the malfunction of
the lower esophageal sphincter, the valve between your
stomach and esophagus. This malfunction .allows the acidic
contents of your stomach to reflux into the sensitive tissue of
the esophagus, producing heartburn. If you commonly use
antacids, gastroenterologists recommend that all coffee, decaf
or regular, should be avoided.
CHEMICAL RESIDUE
When not at home, you can’t be sure what they’re serving you
for decaf in food-service establishments. In fact, many times
when ordering at a restaurant or café, decaf drinkers find that
they are served regular coffee by mistake.
New Choices for Coffee Drinkers
NO-CAF SOLUTIONS
This is the type of herbal tea I drink most frequently. After all,
on a day-to-day basis, we mostly need to keep our good health
intact. If I feel “immune challenged” or I want to start my day
with an immune boost, I’ll drink a cup of a blend that contains
any of the following tonic herbs, known as adaptogens (herbs
that strengthen or enhance the immune system, nervous
system, and/or glandular system while they help the body cope
with stress): Siberian ginseng, Panax ginseng, astragalus,
shizandra, echinacea, ashwagandha, reishi mushrooms,
licorice. Some of my favorite brands include:
• The Republic of Tea: Ginseng Peppermint and Organic
Temple of Health
• Traditional Medicinals: Echinacea Plus, Reishi Defense,
and Double Ginseng
• Celestial Seasonings: Emperor’s Choice, Echinacea
Herb, and Ginseng Plus
• Yogi Tea: Ginseng NRG Tea and Echinacea Special
Formula
DIGESTIVE TEAS
Tnese teas differ from sedative teas because they are designed
to help you cope with stress but not become sleepy. Two herbs
stand out in this arena that have completely different actions
from one another. Siberian ginseng, also called eleuthero
ginseng, has been shown in both animal and human studies to
help the body cope with stress.25 Kava, a muscle relaxant with
a long tradition of use in the South Pacific, can actually help
relieve overtense muscles.26 Kava is one of the new stars on
the herbal market, and you’ll find it in nutritional supplements
and herbal extracts as well as teas. You may want to drink
Siberian ginseng tea frequently, but kava should be saved for
those times when you really need help relaxing and letting go.
For starters:
• The Republic of Tea: Ginseng Peppermint
• Celestial Seasonings: Tension Tamer
• Yogi Tea: Kava Kava Special Formula and Calming Tea
STIMULATING SPICE TEAS
Spices have long been valued for their flavor and stimulating
properties. The spice trade fueled world exploration as
Europeans competed to find exotic flavors and dominate spice-
growing regions. Once spices were as rare and dear as gold,
but now, who could imagine a kitchen without cinnamon,
black pepper, and ginger? Spicy herbal teas will warm you
internally and stimulate your digestion and elimination. Spice
teas have been popular for a long time, but the latest entries
into the marketplace are the spicy “chai” teas inspired by
Indian’s custom of drinking black teas heavily sweetened and
flavored with spice and milk. Chai teas come both as liquid
concentrates and as teas to brew. Some chai brands are
marketing all-herbal blends that are caffeine free. Spice teas in
general require a longer brewing time and are best simmered
for ten minutes to bring out their spicy flavor. They can be
mixed with milk just like black tea.
• Yogi Tea: The original spice tea on the market. Look for
their various blends either Original (loose pack) or in tea
bags with flavors such as Tahitian Vanilla and Hazelnut
Creme.
• The Republic of Tea: Rainforest Tea, Cardamom
Cinnamon, and Cinnamon Chai. Their Republic Chai is
black-tea based.
• Celestial Seasonings: Bengal Spice
• Tazo: Spice
• Sattwa Chai: Herbal Chai Spicy Peppermint
Concentrate and Shanti Herbal
• Oregon Chai and Celestial Seasonings Mountain Chai
are both black-tea based, but offer decaf versions
Sweet Herbs That Save You Calories
There are several herbs whose natural sweetness makes herb
tea blends sweet without added calories.
• Licorice is one of the oldest herbs, used by the Chinese for
thousands of years to harmonize and balance their herbal
formulas. The sweet component of licorice is glycyrrhizin,
which is fifty times sweeter than sugar, so a little goes a long
way. If you have high blood pressure, however, you shouldn’t
drink large quantities of licorice tea, as it can cause the
retention of sodium.
• Stevia, also called sweet herb, is from Paraguay, where the
Guarani Indians have used it for centuries to sweeten their
food. Stevia’s sweet glycoside, called stevioside, is 300 times
sweeter than sugar! With nearly zero calories, it actually
appears to help balance blood sugar levels—great news for
diabetics and those with hypoglycemia. Stevia is now
available as a nutritional supplement, although inexplicably it
is banned in the United States as a sweetener (to protect the
artificial sweetener industry?). Presently, you’ll find stevia in
teas where its sweetness helps bring out the flavor of other
herbs.
• Sweet blackberry leaves come from a special variety of
blackberry that grows in China. Its leaves are sweet only when
picked at the right time of the year, but not as sweet as stevia
or licorice. It has a little more astringency to its flavor. A
recent introduction to the market, sweet blackberry hasn’t been
studied as extensively as stevia or licorice.
FRUIT TEAS
In Europe, fruit teas are the most popular type of herbal tea
blends. Fruit teas usually have hibiscus flowers, orange peel,
rose hips, and sometimes lemon grass in their base. The teas
can contribute significant vitamin C to your diet, and they are
delicious iced. Because they usually have a strong citrus
accent, they are refreshing and thirst quenching. There are so
many flavors of fruit teas, with multiple brands marketed by
the same company, that you’ll have to experiment to see which
are your favorites. Here are some of mine:
• The Republic of Tea: Alpine Flowers Tea, Lemon
Wintergreen, Kid’s Cuppa, and Organic Flowering Fruit
herb tea
• Tazo: Passion and Wild Sweet Orange
• Celestial Seasonings: Any of the Zinger blends in the
fruit flavor of your choice
ROOIBOS TEA
2. Replacement: Some people find that this works, but it has to be done carefully. If you
consume four cups of coffee a day, don’t assume that you can have your first two cups and simply
replace the last two cups with herbal tea.
That will still produce a radical drop in blood caffeine levels, triggering a withdrawal headache. For
the replacement method to work, you have to figure out how to maintain a normal (for you) level of
caffeine in your blood while you gradually reduce that level over a two-week period. That’s most
easily done by alternating coffee and caffeine free beverages.
Example: Many people have two cups of coffee in the morning, another at midmorning, and
their final cup with lunch or afternoon coffee break. A rapid drop in blood caffeine levels can be
avoided by having cup #1 at the customary morning time, but replace cup #2 with decaf, herb tea,
coffee substitute, herbal coffee, or hot soup. The mid-morning coffee would be continued, and the
alternative would be used at the afternoon coffee break.
Then, of course, one needs to reduce the caffeine intake at the morning and midmorning time
points. Here are a few tips:
[Link] your coffee with 50 percent decaf. Some companies produce coffee blends with a
fifty-fifty mix of decaf and caffeinated coffee. After a week or so, you will need to add
increasing amounts of decaf until you are ultimately using 100 percent decaf. Don’t forget,
decaf still contains some caffeine, as well as harsh acids and oils inherent in the coffee
bean (see Chapter 9). You might do better by ultimately switching to herb tea, herbal
coffee, or another coffee alternative.
B. Get a smaller coffee mug. One client of mine had a revelation when we were exploring
the cause of her fatigue and anxiety. She started noticing increased fatigue shortly after
turning thirty, and of course she (and her doctor) attributed it to “getting older.” But as she
and I looked at a possible coffee connection, she burst out laughing. “That’s it,” she cried.
“For my thirtieth birthday, a friend gave me a coffee mug with one of those cute ‘Now that
you’re over the hill…’ inscriptions. This new mug was huge, but I filled it and drank it
twice a day as I had with my old mug.” Unknowingly, this woman had nearly doubled her
caffeine intake and was suffering the consequences.
Well, it works the other way, too. Most of us just want to have a mug of some good-tasting,
hot beverage, and the size of the mug doesn’t matter all that much. So downsize your mug
(avoid refills) and that will help reduce your caffeine intake.
C. Make your coffee weaker. Whether you brew your coffee or use instant, you can
gradually decrease the amount you use.
D. Add more milk. If you already take milk with your coffee, simply add more. If this is not
your habit, give it a try. Adding low-fat milk reduces the amount of coffee in the cup and
therefore decreases your caffeine intake. Plus the milk provides a valuable source of
calcium and protein.
Chapter 1
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Chapter 2
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Chapter 3
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45 D. M. Hilker, K. Chan, R. Chen et al., “Antithiamine Effects of Tea,” Nutrition Reports
International, 1971;4:223–27. (back to text)
46V. Tanphaichitr and B. Wood, “Thiamin,” in Present Knowledge in Nutrition, fifth edition
(Washington D.C.: Nutrition Foundation, 1984), pp. 273–84. (back to text)
47S. L. Vimokesant, S. Kunjara et al. “Beri-beri Caused by Antithiamin Factors in Food and Its
Prevention,” Annals of the New York Academy of Sciences, 1982;378:123–36. (back to text)
48L. Massey and T. Berg, “The Effect of Dietary Caffeine on Urinary Excretion of Calcium,
Magnesium, Phosphorus, Sodium, Potassium, Chloride and Zinc in Healthy Males,” Nutrition
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49Neuhauser-Berthold, S. Beine, C. Verwied et al., “Coffee Consumption and Total Body Water
Homeostasis as Measured by Fluid Balance and Bioelectrical Impedance Analysis,” Annals of
Nutrition and Metabolism, 1997;41(1):29–36. (back to text)
50P. Hollingberry and L. Massey, “Effects of Dietary Caffeine and Sucrose on Urinary Calcium
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51
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Minerals in Adult Women,” Life Sciences, 1990;47(6):557–64. (back to text)
52 K. Van Dyck, S. Tas, H. Robberecht et al., “The Influence of Different Food Components on the
In Vitro Availability of Iron, Zinc and Calcium from a Composed Meal,” International Journal of
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53 G. Wyshak, R. E. Frisch, T. E. Albright et al., “Non-alcoholic Carbonated Beverage Consumption
among Women Former Collegiate Athletes,” Journal of Orthopedic Research, 1989:7:91–99. (back
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54G. Wyshak and R. E. Frisch, “Carbonated Beverages, Dietary Calcium, the Dietary
Calcium/Phosphorus Ratio, and Bone Fractures in Girls and Boys,” Journal of Adolescent Health,
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55N. Kojima, D. Wallace and G. W. Bates, “The Effect of Chemical Agents, Beverages, and
Spinach on the In Vitro Solubilization of Iron from Cooked Pinto Beans,” American Journal of
Clinical Nutrition, 1981;34:1392–l401. (back to text)
56T. A. Morck, S. R. Lynch, and J. D. Cook, “Inhibition of Food Iron Absorption by Coffee,”
American Journal of Clinical Nutrition, 1983;37:416–20. (back to text)
57 G. B. Gabrielli and G. De Sandre, “Excessive Tea Consumption Can Inhibit the Efficacy of Oral
Iron Treatment in Iron-Deficiency Anemia,” Haematologica, November 1995;80(66):518–20. (back
to text)
58A. C. Bancu, M. Gherman et al., “Regulation of Human Natural Cytotoxicity by IgG. II: Cyclic
AMP as a Mediator of Monomeric IgG-induced Inhibition of Natural Killer Cell Activity,” Cellular
Immunology, 1988:114(2):246. (back to text)
59P. T. Paradowski and K. Zeman, “Pentoxifylline,” Postepy Higieny Imedycyny Doswiadczalnej,
1995;49(2):201–20. (back to text)
60G. Gatti, R. Cavallo, M. L. Sartori et al. “Inhibition by Cortisol of Human Natural Killer (NK)
Cell Activity,” Journal of Steroid Biochemistry, January 1987;26(1):49–58. (back to text)
61H. N. Baybutt and F. Holsboer, “Inhibition of Macrophage Differentiation and Function by
Cortisol,” Endocrinology, July 1990;127(1):476–80. (back to text)
62O. Khorram, L. Vu, and S. S. Yen, “Activation of Immune Function by Dehy-droepiandrosterone
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63J. A. McLachlan, C. D. Serkin, and O. Bakouche, “Dehydroepiandrosterone Modulation of
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64 R. J. Reiter, D. X. Tan, B. Poeggeler et al., “Melatonin as a Free Radical Scavenger: Implications
for Aging and Age-Related Diseases,” Annals of the New York Academy of Sciences, 1994;719:1–
12. (back to text)
65 G. J. Maestroni and A. Conti, “Immuno-derived Opiods as Mediators of the Immuno-enhancing
and Anti-stress Action of Melatonin,” Ada Neurologica (Napoli), August 1991;13(4):356–60. (back
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66P. Monteleone, A. Fuschino, G. Nolfe et al., “Tempotal Relationship between Melatonin and
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67G. Heuther, “Melatonin Synthesis in the Gastrointestinal Tract and the Impact of Nutritional
Factors on Circulating Melatonin,” Annals of the New York Academy of Sciences, 1994;719:146–58.
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68K. P. Wright, Jr., P. Badia, B. L. Myers et al., “Caffeine and Light Effects on Nighttime Melatonin
and Temperature Levels in Sleep-deprived Humans,” Brain Research, January 30, 1997;747(1):78–
84. (back to text)
69
S. M. Armstrong and J. R. Redman, “Melatonin: A Chronobiotic with Anti-aging Properties?”
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70W. Pierpaoli and V. Lesnikov, “The Pineal Aging Clock,” Annals of the New York Academy of
Sciences, 1994;719:461–71. (back to text)
71J. E. Blalock, E. M. Smith, and W. J. Meyer, 3rd., “The Pituitary-adrenocortical Axis and the
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T. L. Pruett and E B. Cerra, “The Physiologic and Metabolic Responses to Stress and Sepsis,”
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Chapter 4
1 W. R. Lovallo, M. Al’Absi, K. Blick et al., “Stress-like Adrenocorticotropin Responses to Caffeine
in Young Healthy Men,” Pharmacology; Biochemistry and Behavior, November 1996;55(3):365–
69. (back to text)
2I. Iancu, O. T. Dolberg, and J. Zohar, “Is Caffeine Involved in the Pathogenesis of Combat-stress
Reaction?” Military Medicine, April 1996;161(4):230–32. (back to text)
3P. Cotton, “Neurophysiology and Philosophy,” Journal of the American Medical Association,
1993;269(12):1485–86. (back to text)
4D. J. Roca, G. D. Schiller, and D. H. Farb, “Chronic Caffeine or Theophylline Exposure Reduces
Gamma-aminobutyric Acid/Benzodiazepine Receptor Site Interactions,” Molecular Pharmacology,
May 1988;33(5):481–85. (back to text)
5L. N. Robins et al., “Lifetime Prevalence of Specific Psychiatric Disorders in Three Sites,”
Archives of General Psychiatry, 1984;41:949–58. (back to text)
6O. G. Cameron and R. M. Nesse, “Systemic Hormonal and Physiological Correlations in Anxiety
Disorders,” Psychoneuroendocrinology, 1988;13(4):287–307. (back to text)
7F. A. Wiesel, “Positron Emission Tomography in Psychiatry,” Psychiatric Developments, 1989,
Spring;7(1):19–47. (back to text)
8 T. Kuboki and H. Suematsu, “Panic Disorder,” Nippon Rinsho, November 1992:50(11):2773–82.
(back to text)
9H. M. van Praag, “Central Monoamine Metabolism in Depression II: Catecholamines and Related
Compounds,” Comprehensive Psychiatry, 1980;21(1):44–54. (back to text)
10J. M. Gorman and M. R. Liebowitz, “Panic and Anxiety Disorders,” in R. Michels et al. (eds.),
Psychiatry, vol. 1 (Philadelphia: J. B. Lippincott, 1985), pp. 1–13. (back to text)
11R. J. Matthew and W. H. Wilson, “Behavioral and Cerebrovascular Effects of Caffeine in Patients
with Anxiety Disorders,” Acta Psychiatrica Scandinavica, July 1990;82(1):17–22. (back to text)
12M. C. McManamy and P. G. Schube, “Caffeine Intoxication,” New England Journal of Medicine,
1936;215:616–20. (back to text)
13P. P. Roy-Byrne and T. W. Uhde, “Exogenous Factors in Panic Disorder: Clinical and Research
Implications,” Journal of Clinical Psychiatry, February 1988;49(2):56–61. (back to text)
14A. Breier, D. S. Charney, and G. R. Heninger, “Agoraphobia with Panic Attacks: Development,
Diagnostic Stability, and Course of Illness,” Archives of General Psychiatry, November
1986;43(11):1029–36. (back to text)
15M. A. Lee, P. Flegel, J. F. Greden et al., “Anxiogenic Effects of Caffeine on Panic and Depressed
Patients,” American Journal of Psychiatry, May 1988;145(5):632–35. (back to text)
16 J. P. Boulanger et al., “Increased Sensitivity to Caffeine in Patients with Panic Disorder,” Archives
of General Psychiatry, 1984;41:1067–71. (back to text)
17D. S. Charney, G. R. Heninger, and P. I. Jatlow, “Increased Anxiogenic Effects of Caffeine in
Panic Disorders,” Archives of General Psychiatry, March 1985;42(3):233–43. (back to text)
18 D. V. Sheehan, J. C. Ballenger, and G. Jacobsen, “Treatment of Endogenous Anxiety with Phobic,
Hysterical and Hypochondriacal Symptoms,” Archives of General Psychiatry, 1980;37:51–59. (back
to text)
19 J. D. Lane, R. A. Adcock, R. B. Williams et al., “Caffeine Effects on Cardiovascular and
Neuroendocrine Responses to Acute Psychosocial Stress and Their Relationship to Level of
Habitual Caffeine Consumption,” Psychosomatic Medicine, May-June 1990;52(3):320–36. (back to
text)
20D. C. Mackay and J. W. Rollins, “Caffeine and Caffeinism,” Journal of the Royal Navy Medical
Service, 1989;75(2):65–67. (back to text)
21J. R. Hughes, S. T. Higgins, W. K. Bickel et al., “Caffeine Self-Administration, Withdrawal, and
Adverse Effects among Coffee Drinkers,” Archives of General Psychiatry, July 1991;48(7):611–17.
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22J. D. Lane, “Effects of Brief Caffeinated-beverage Deprivation on Mood, Symptoms, and
Psychomotor Performance,” Pharmacology, Biochemistry and Behavior, September
1997;58(1):203–08. (back to text)
23K. Silverman, S. M. Evans, E. C. Strain et al., “Withdrawal Syndrome after the Double-blind
Cessation of Caffeine Consumption,” New England Journal of Medicine, October 15,
1992;327(16):1109–14. (back to text)
24 “Pharmacology Update,” Internal Medicine Alert, 1992;14(1):7. (back to text)
25M. Weissman, “Epidemiology of Depression: Frequency, Risk Groups, and Risk Factors,” in
Perspectives on Depressive Disorders: A Review of Recent Research (Washington, D.C.: National
Institute of Mental Health, 1986). (back to text)
26D. A. Regier, R. M. A. Hirschfeld, and F. K. Goodwin, “The NIMH Depression Awareness,
Recognition and Treatment (D/ART) Program: Structure, Aims and Scientific Basis,” American
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27“Caffeine Can Increase Brain Serotonin Levels,” Nutrition Reviews, October 1988;46(10):366–
67. (back to text)
28K. Silverman, S. M. Evans, E. C. Strain et al., “Withdrawal Syndrome after the Double-blind
Cessation of Caffeine Consumption,” New England Journal of Medicine, October 15, 1992;327(16):
1109–14. (back to text)
29R. Caccioatore, A. Helbling, C. Jost et al., “Episodic Headache, Diminished Performance and
Depressive Mood” (in German), Schweizerische Rundschau for Medizin Praxis, May 28,
1996;85(22):727–29. (back to text)
30L. Tondor, N. Rudhause et al., “Course of Seasonal Bipolar Disorder Influenced by Caffeine,”
Journal of Affective Disorders, 1991;22:249–51. (back to text)
31W. H. Frishman, “Beta-adrenergic Blockers,” Medical Clinics of North America, 1988;72:37.
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32 Physicians’ Desk Reference, 44th edition, 1990. (back to text)
33 Pharmacotherapy, 1987;7:1–15. (back to text)
34M. A. Lee, P. Flegel, J. F. Greden et al., “Anxiogenic Effects of Caffeine on Panic and Depressed
Patients,” American Journal of Psychiatry, May 1988;145(5):632–35. (back to text)
35 T. Kuboki and H. Suematsu, “Panic Disorder,” Nippon Rinsho, May 1994;52(5):1334–38. (back
to text)
36J. F. Mortola, J. H. Liu, J. C. Gillin et al., “Pulsatile Rhythms of Adrenocorticotropin (ACTH) and
Cortisol in Women with Endogenous Depression: Evidence for Increased AOTH Pulse Frequency,”
Journal of Clinical Endocrinology and Metabolism, November 1987;65(5):962–68. (back to text)
37M. Vollrath, W. Wicki, and J. Angst, “The Zurich Study VIII: Insomnia: Association with
Depression, Anxiety, Somatic Syndromes, and Course of Insomnia,” European Archives of
Psychiatry and Neurological Sciences, 1989;239(2):113–24. (back to text)
38D. J. Haleem, A. Yasmeen, M. A. Haleem et al., “24 hour Withdrawal Following Repeated
Administration of Caffeine Attenuates Brain Serotonin but Not Tryptophan in Rat Brain:
Implications for Caffeine-Induced Depression,” Life Sciences, September 29, 1995;57(19):PL285–
92. (back to text)
39T. C. Neylan, “Treatment of Sleep Disturbances in Depressed Patients,” Journal of Clinical
Psychiatry, 1995;56 supplement 2:56–61. (back to text)
40Anon. “The Impact of Stress on the Recurrence of Bipolar Episodes,” Family Practice
Recertification, 1992;14(2):412. (back to text)
41P J. O’Connor, W. P. Morgan, J. S. Raglin et al., “Mood State and Salivary Cortisol Levels
Following Overtraining in Female Swimmers,” Psychoneuroendocrinology, 1989;14(4):303–10.
(back to text)
42E. Leibenluft, P. L. Fiero, J. J. Bartko et al., “Depressive Symptoms and the Self-reported Use of
Alcohol, Caffeine, and Carbohydrates in Normal Volunteers and Four Groups of Psychiatric
Outpatients,” American Journal of Psychiatry, February 1993; 150(2) :294–301. (back to text)
43T. C. Neylan, “Treatment of Sleep Disturbances in Depressed Patients,” American Journal of
Clinical Psychiatry, 1995;56 supplement 2:56–61. (back to text)
44E. Susman, “Prozac May Rob You of a Good Night’s Sleep,” Medical Tribune News Service;
September 16, 1997. (back to text)
45J. D. Morrison, “Fatigue as a Presenting Complaint in Family Practice,” Journal of Family
Practice, 1980;10:795. (back to text)
46S. Findlay, “New Hope for Tired People,” U.S. News & World Report, October 31, 1988:71–73.
(back to text)
47W. S. Terry and B. Phifer, “Caffeine and Memory Performance on the AVLT,” Journal of Clinical
Psychology, November 1986;42(6):860–3. (back to text)
48R. Gilliland and D. Andress, “Ad Lib Caffeine Consumption, Symptoms of Caffeinism, and
Academic Performance,” American Journal of Clinical Psychiatry, April 1981;138(4):512–14.
(back to text)
49J. R. Bradley and A. Petree, “Caffeine Consumption, Expectancies of Caffeine-enhanced
Performance, and Caffeinism Symptoms among University Students,” Journal of Drug Education,
1990;20(4):319–28. (back to text)
50C. H. Ashton and F. Kamali, “Personality, Lifestyles, Alcohol and Drug Consumption in a
Sample of British Medical Students,” Medical Education, May 1995;29(3):187–92. (back to text)
51G. A. Pincomb, W. R. Lovallo, R. B. Passey et al., “Caffeine Enhances the Physiological
Response to Occupational Stress in Medical Students,” Health Psychology, 1987;6(2): 101–12.
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52R. T. Cox, and R. J. Walker, “An Analysis of the Adenosine Receptors Responsible for
Modulation of an Excitatory Acetylcholine Response on an Identified Helix Neuron,” Comparative
Biochemistry and Physiology, C: Comparative Pharmacology and Toxicology, 1987;88(1):121–30.
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53O. Nikodijevic, K. A. Jacobson, and J. W. Daly, “Locomotor Activity in Mice During Chronic
Treatment with Caffeine and Withdrawal,” Pharmacology, Biochemistry and Behavior, January
1993;44(1):199–216. (back to text)
54L. Linde, “An Auditory Attention Task: A Note on the Processing of Verbal Information,”
Perceptual and Motor Skills, April 1994;78(2):563–70. (back to text)
55O. G. Cameron, J. G. Modell, and M. Hariharan, “Caffeine and Human Cerebral Blood Flow: A
Positron Emission Tomography Study,” Life Sciences, 1990;47(13):1141–46. (back to text)
56R. J. Matthew and W. H. Wilson, “Substance Abuse and Cerebral Blood Flow,” American
Journal of Psychiatry, March 1991;148(3):292–305. (back to text)
57A. Nehlig, J. L. Daval, and G. Debry, “Caffeine and the Central Nervous System: Mechanisms of
Action, Biochemical, Metabolic and Psychostimulant Effects,” Brain Research Reviews, May–
August 1992;17(2):139–70. (back to text)
58J. C. Galduroz and E. A. Carlini, “The Effects of Long-term Administration of Guarana on the
Cognition of Normal, Elderly Volunteers,” Revista Paulista de Medicina, January–February 1996;
114(1): 1073–78. (back to text)
59J. C. Galduroz and E. de A. Carlini, “Acute Effects of the Paulinia cupana, ‘Guarana,’ on the
Cognition of Normal Volunteers,” Revista Paulista de Medicina, July–September 1994;112(3):607–
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60O. M. Wolkowitz, V. I. Reus, E. Roberts et al., “Dehydroepiandrosterone (DHEA) Treatment of
Depression,” Biological Psychiatry, 1997:41:311–18. (back to text)
61D. M. Diamond, B. J. Branch, M. Fleshner et al., “Effects of Dehydroepiandrosterone Sulfate and
Stress on Hippocampal Electrophysiological Plasticity,” Annals of the New York Academy of
Science, 1995;774:304–07. (back to text)
62 J. Ferri, “Under Pressure,” Tampa Tribune-Times, April 27, 1997; p. 1. (back to text)
63S. L. Dubovsky, “Generalized Anxiety Disorder: New Concepts and Psychopharmacologic
Therapies,” Journal of Clinical Psychiatry, January 1990;51 supplement:3–10. (back to text)
64A. Koczapski, J. Paredes, C. Kogan et al., “Effects of Caffeine on Behavior of Schizophrenic
Inpatiems,” Schizophrenia Bulletin, 1989:15(2)339–4. (back to text)
65T. J. Crowley, D. Chesluk, S. Dilts et al., “Drug and Alcohol Abuse among Psychiatric
Admissions—Multidrug Clinical-toxicologic Study,” Archives of General Psychiatry, 1974;30:13–
20. (back to text)
66 M. Rihs, C. Muller, and P. Baumann, “Caffeine Consumption in Hospitalized Psychiatric
Patients,” European Archives of Psychiatry and Clinical Neuroscience, 1996;246(2):83–92. (back to
text)
67D. C. Mackay and J. W. Rollins, “Caffeine and Caffeinism,” Journal of the Royal Naval Medical
Service, Summer 1989:75(2):65–67. (back to text)
68
A. Kruger, “Chronic Psychiatric Patients’ Use of Caffeine: Pharmacological Effects and
Mechanisms,” Psychological Reports, June 1996;78(pt 1):915–23. (back to text)
69P. B. Lucas, D. Pickar, J. Kelsoe et al., “Effects of the Acute Administration of Caffeine in
Patients with Schizophrenia,” Biological Psychiatry, July 1, 1990;28(1):35–40. (back to text)
70G. F. Searle, “The Effect of Dietary Caffeine Manipulation on Blood Caffeine, Sleep and
Disturbed Behaviour,” Journal of ‘Intellectual Disability Research, August 1994;38(pt 4):383–91.
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71J. F. Greden, “Anxiety or Caffeinism: A Diagnostic Dilemma,” American Journal of Psychiatry,
1974; 131:1089. (back to text)
72K. Nishihara and K. Mori, “The Differences of Self-ratings of Sleep Quality Associated with
Epinephrine and Wake Time During 4-Hour Sleep,” Psychiatry and Clinical Neuroscience, October
1996;50(5):277–83. (back to text)
73M. H. Bonnet and D. L. Arand, “The Consequences of a Week of Insomnia,” Sleep, July
1996;19(6):453–61. (back to text)
74B. V. Reifler, “Depression, Anxiety, and Sleep Disturbances,” International Psychogeriatrics,
1996;8 supplement 3:415–18. (back to text)
75T. Q. Miller, T. W. Smith, C. W. Turner et al., “A Meta-analytic Review of Research on Hostility
and Physical Health,” Psychological Bulletin, March 1996;119(2):322–48. (back to text)
76M. Wald, “Violent Aggressive Motorists Account for 28,000 Deaths,” New York Times News
Service, July 1997. (back to text)
77 D. K. Dekker, M. J. Paley, S. M. Popkin et al., “Locomotive Engineers and Their Spouses: Coffee
Consumption, Mood, and Sleep Reports,” Ergonomics, January–March 1993;36(1–3)233–38. (back
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78G. V. Hughes and F. J. Boland, “The Effects of Caffeine and Nicotine Consumption on Mood and
Somatic Variables in a Penitentiary Inmate Population,” Addictive Behaviors, September–October
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79K. Raikkonen, A. Hautanen, and L. Keltikangas-Jarvinen, “Feelings of Exhaustion, Emotional
Distress, and Pituitary and Adrenocortical Hormones in Borderline Hypertension,” Journal of
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80P. Jin, “Changes in Heart Rate, Noradrenaline, Cortisol and Mood during Tai Chi,” Journal of
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81A. McGrady, M. Woerner, G. A. Bernal et al., “Effect of Biofeedback-assisted Relaxation on
Blood Pressure and Cortisol Levels in Normotensives and Hypertensives,” Journal of Behavioral
Medicine, June 1987;10(3):301–10. (back to text)
82G. A. Smith, “Caffeine Reduction as an Adjunct to Anxiety Management,” British Journal of
Clinical Psychology, 1988;27:265–66. (back to text)
Chapter 5
1 American Medical News, January 27, 1992, p. 20. (back to text)
2W. R. Lovallo, G. A. Pincomb, B. H. Sung et al., “Hypertension Risk and Caffeine’s Effect on
Cardiovascular Activity during Mental Stress in Young Men,” Health Psychology, 1991;10(4):236–
43. (back to text)
3J. M. MacDougall, L. Musante, S. Castillo et al., “Smoking, Caffeine, and Stress: Effects on Blood
Pressure and Heart Rate in Male and Female College Students,” Health Psychology, 1988;7(5):46l–
78. (back to text)
4J. P. Henry and J. C. Cassel, “Psychosocial Factors in Essential Hypertension: Recent
Epidemiological and Animal Experimental Evidence,” American Journal of Epidemiology,
1969;90:171–200. (back to text)
5 G. A. Pincomb, W. R. Lovallo, R. B. Passey et al., “Effect of Behavior State on Caffeine’s Ability
to Alter Blood Pressure,” American Journal of Cardiology, April 1, 1988;61(10):798–802. (back to
text)
6W. R. Lovallo, M. al’Absi, G. A. Pincomb et al., “Caffeine and Behavioral Stress Effects on Blood
Pressure in Borderline Hypertensive Caucasian Men,” Health Psychology, January 1996;15(1):11–
17. (back to text)
7P. J. Green and J. Suls, “The Effects of Caffeine on Ambulatory Blood Pressure, Heart Rate, and
Mood in Coffee Drinkers,” Journal of Behavioral Medicine, April 1996;19(2):111–28. (back to text)
8 J. Ratliff-Crain, M. K. O’Keeffe, and A. Baum, “Cardiovascular Reactivity, Mood, and Task
Performance in Deprived and Nondeprived Coffeedrinkers,” Health Psychology, 1989;8(4):427–47.
(back to text)
9P. Smits, T. Thein, and A. van’t Laar, “Coffee and the Human Cardiovascular System,”
Netherlands Journal of Medicine, 1987;31(7):36. (back to text)
10C. R. Lake, G. Zaloga, J. Bray et al., “Transient Hypertension after Two Phenylpropanolamine
Diet Aids and the Effects of Caffeine: A Placebo-controlled Follow-up Study,” American Journal of
‘Medicine, April 1989;86(4):427–32. (back to text)
11 S. S. Chua and S. I. Benrimoj, “Non-prescription Sympathomimetic Agents and Hypertension,”
Medical Toxicology and Adverse Drug Experience, September–October 1988;3(5):387–417. (back
to text)
12S. C. Dilsaver, N. A. Votolato, and N. E. Alessi, “Complications of Phenyl-propanolamine,”
American Family Physician, April 1989;39(4):201–06. (back to text)
13 M. A. Sloan, S. J. Kittner, D. Rigamonti et al., “Occurrence of Stroke Associated with Use/Abuse
of Drugs,” Neurology, September 1991;41(9):1358–64. (back to text)
14C. R. Lake, D. B. Rosenberg, S. Gallant et al., “Phenylpropanolamine Increases Plasma Caffeine
Levels,” Clinical Pharmacology and Therapeutics, June 1990;47(6):675–85. (back to text)
15C. R. Lake, “Manic Psychosis after Coffee and Phenylpropanolamine,” Biological Psychiatry,
August 15, 1991;30(4):401–04. (back to text)
16E. Casiglia, S. Bongiovi, C. D. Paleari et al., “Haemodynamic Effects of Coffee and Caffeine in
Normal Volunteers: A Placebo-controlled Clinical Study,” Journal of Internal Medicine, June
1991;229(6):501–04. (back to text)
17B. H. Sung, W. R. Lovallo, G. A. Pincomb et al., “Effects of Caffeine on Blood Pressure
Response during Exercise in Normotensive Healthy Young Men,” American Journal of Cardiology,
April 1, 1990;65(13):909–13. (back to text)
18G. A. Pincomb, M. F. Wilson, B. H. Sung et al., “Effects of Caffeine on Pressor Regulation
during Rest and Exercise in Men at Risk for Hypertension,” American Heart Journal, October
1991;122(pt 1):1107–15. (back to text)
19K. J. Wise, E. A. Bergman, D. J. Sherrard et al., “Interactions between Dietary Calcium and
Caffeine Consumption on Calcium Metabolism in Hypertensive Humans,” American Journal of
Hypertension, March 1996;9(3):223–29. (back to text)
20 J. D. Kark, Y. Friedlander, N. A. Kaufmann et al., “Coffee, Tea and Plasma Cholesterol: The
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149J. Haase, P. Halama, and R. Horr, “Effectiveness of Brief Infusions with Ginkgo biloba Special
Extract in Dementia of the Vascular and Alzheimer Type,” Zeitschrift fur Gtmntogie und Geriatrie,
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150M. Fennelly, D. C. Galletly, and G. I. Purdei, “Is Caffeine Withdrawal the Mechanism of
Postoperative Headache?” Anesthesia and Analgesia, April 1991;72(4):449–53. (back to text)
151J. G. Weber, J. T Klindworth, J. J. Arnold et al., “Prophylactic Intravenous Administration of
Caffeine and Recovery after Ambulatory Surgical Procedures,” Mayo Clinic Proceedings, July
1997;72(7):621–26. (back to text)
152Neuhauser-Berthold, S. Beine, S. C. Verwied et al., “Coffee Consumption and Total Body Water
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153
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154“Effect of Environmental Temperature on the Toxicity of Caffeine and Dextroam-phetamine in
Mice,” Journal of Pharmacology and Experimental Therapeutics, January 1970;171(1):153–58.
(back to text)
155P. J. Muller and J. Vernikos-Danellis, “Alteration in Drug Toxicity by Environmental Variables,”
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156
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157Y. Ohsaki, S. Ishida, T. Fujikane et al., “Combination Effect of Caffeine and Cisplatin on a
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158 J. A. Carrillo and J. Benitz, “CYP1A2 Activity, Gender and Smoking as Variables Influencing
the Toxicity of Caffeine,” British Journal of Clinical Pharmacology, June 1996;41(6):605–08. (back
to text)
159H. Shear, S. P. Spielberg, D. M. Grant et al., “Differences in Metabolism of Sulfonamides
Predisposing to Idiosyncratic Toxicity,” Annals of Internal Medicine, August 1986;105(2):179–84.
(back to text)
160M. Rieder, N. H. Shear, A. Kanee et al., “Prominence of Slow Acetylator Phenotype among
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161J. E. Trosko and H. Y. Chu, “Inhibition of Repair of UV-damaged DNAby Caffeine and
Mutation Induction in Chinese Hamster Cells,” Chemico-Biological Interactions, 1973:6:317–32.
(back to text)
162 A. Antoccia, R. Ricordy, P. Maraschio et al., “Chromosomal Sensitivity to Clasto-genic Agents
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163P. J. Donovan and J. A. DiPaolo, “Caffeine Enhancement of Chemical Carcinogen-induced
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164L. L. Anderson, C. C. Lau, E. J. Gtacely et al., “Enhancement of 1311-mediated Cytotoxicity by
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165C. Petit, “Wake Up and Smell Health Benefits of Fresh Coffee,” San Francisco Chronicle, April
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166
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Hydroxyl Radicals,” Food and Chemical Toxicology, January 1991;29(l):1–6 (back to text)
167T. P. Devasagayam, J. P. Kamat, H. Mohan et al., “Caffeine as an Antioxidant: Inhibition of
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168K. P. Wright, Jr., P. Badia, B. L. Myers et al., “Caffeine and Light Effects on Nighttime
Melatonin and Temperature Levels in Sleep-deprived Humans,” Brain Research, January 30,
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169 P. C. Konturek, S. J. Konturek, T. Brzozowski et al., “Gastroprotective Activity of Melatonin and
Its Precursor, L-tryptophan, against Stress-induced and Ischaemia-induced Lesions Is Mediated by
Scavenge of Oxygen Radicals,” Scandinavian Journal of Gastroenterology, May 1997;32(5):433–
38. (back to text)
170W. U. Mullet, T. Bauch, A. Wojcik et al., “Comet Assay Studies Indicate that Caffeine-mediated
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171
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172V. V. Frolkis, “Stress-age Syndrome,” Mechanisms of Ageing and Development, June
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173S. Hoyer, “Age-related Changes in Cerebral Oxidative Metabolism: Implications for Drug
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174R. M. Sapolsky, “Why Stress Is Bad for Your Brain,” Science, August 9, 1996;273(5276):749–
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175G. Gatti, R. Cavallo, M. L. Sartori et al., “Inhibition by Cortisol of Human Natural Killer (NK)
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176J. E. Blalock et al., “The Pituitary-adtenocortical Axis and the Immune System,” Clinical
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177H. J. Naurath, E. Joosten, R. Riezler et al., “Effects of Vitamin B12, Folate, and Vitamin B6
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178
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179G. Schmid-Ott, R. Jacobs, B. Jager et al., “Stress-induced Endocrine and Immuno-logical
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180D. Christensen, “Diabetes at All-time High in U.S.,” Medical Tribune News Service, October 30,
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181L. Vergauwen, P. Hespel, and E. A. Richter, “Adenosine Receptors Mediate Synergistic
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182M. Sachs and H. Forster, “Effect of Caffeine on Various Metabolic Parameters In Vivo,”
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183 J. Portugal-Alvarez, A. Zamarron, J. Yanguela et al., “Lipolysis Induced by Coffee and Tobacco:
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184 O. Vaccaro, D. Ingrosso, A. Rivellese et al., “Moderate Hyperhomocysteinaemia and
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185S. Neugenbauer, T. Baba, K. Kurokawa et al., “Defective Homocysteine Metabolism as a Risk
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186 C. Lehman, J. Rodin, B. S. McEwen et al., “Impact of Environmental Stress on the Expression
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187K. Raikkonen, L. Keltikangas-Jarvinen, H. Aldercreutz et al., “Psychosocial Stress and the
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188J. Tuomilehto, E. Tuomilehto-Wolf, R. LaPorte et al., “Coffee Consumption as Trigger for
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189D. Kerr, R. S. Sherwin, F. Pavalkis et al., “Effect of Caffeine on the Recognition of and
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190 P. McAdam, “Caffeine May Trigger Hypoglycemia,” Medical Tribune, 1993; 34(21):21. (back to
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191 Ibid. (back to text)
192
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193 J. B. Corcuff, P. Lafranque, P. Henry et al., “Isolated Cortiocotroph Insufficiency Associated to
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194D. Buchwald, J. Umali, M. Stene, “Insulin-like Growth Factor-I (Somatomedin C) Levels in
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195 R. G. Lahita, “The Connective Tissue Diseases and the Overall Influence of Gender,”
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to text)
196R. F. van Vollenhoven, L. M. Morabito, E. G. Engleman et al., “Treatment of Systemic Lupus
Erythematosus with Dehydroepiandrosterone: 50 Patients Treated up to 12 Months,” Journal of
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197 M. Kodama, T. Kodama, and M. Murakami, “The Value of the Dehydroepiandrosterone-annexed
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198 S. J. Pollard, S. L. Spector, S. W. Yancey et al., “Salmeterol versus Theophylline in the
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199
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200J. T. Barr, G. E. Schumacher, D. B. Luks et al., “MildTheophylline-related Adverse Reactions
and Serum Theophylline Concentration,” American Journal of Hospital Pharmacy, November 1,
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201B. C. Bandyopadhyay and M. K. Poddar, “Theophylline-induced Changes in Mammalian
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202H. Segawa and Y. Iikura, “Clinical Effects of Theophylline in the Therapy of Intractable
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203
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204L A. Coskey, J. Bitting, and M. D. Roth, “Inhibition of Natural Killer Cell Activity by
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205T. Caballero, C. Garcia-Ara, C. Pascual et al., “Urticaria Induced by Caffeine,” Journal of
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206L. J. Crofford, S. R. Pillemer, K. T. Kalogeras et al., “Hypothalamic-Pituitary-Adrenal Axis
Perturbations in Patients with Fibromyalgia,” Arthritis and Rheumatism, November
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207 E. N. Griep, J. W. Boersma, and E. R. de Kloet, “Altered Reactivity of the Hypothalamic-
Pituitary-Adrenal Axis in the Primary Fibromyalgia Syndrome,” Journal of Rheumatology, March
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208L. J. Crofford, N. C. Engleberg, and M. A. Demitrack, “Neurohormonal Perturbations in
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209J. C. van Denderen, J. W. Boersma, P. Zeinstra et al., “Physiological Effects of Exhaustive
Physical Exercise in Primary Fibromyalgia Syndrome (PFS): Is PFS a Disorder of Neuroendocrine
Reactivity?” Scandinavian Journal of Rheumatology, 1992;21(1):35–37. (back to text)
210M. Kennedy and D. T. Felson, “A Prospective Long-term Study of Fibromyalgia Syndrome,”
Arthritis and Rheumatism, April 1996;39(4):682–85. (back to text)
211“Fibromyalgia,” in S. Margolis and H. Moses (eds.), The Johns Hopkins Medical Handbook
(New York: Random House), pp. 371–75. (back to text)
212J. Bearn, T. Allain, P. Coskeran et al., “Neuroendocrine Responses to D-fenfluramine and
Insulin-induced Hypoglycemia in Chronic Fatigue Syndrome,” Biological Psychiatry, February 15,
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213P. Strickland, R. Morriss, A. Wearden et al., “A Comparison of Salivary Cortisol in Chronic
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214 L. V. Scott and T. G. Dinan, “Urinary Free Cortisol Excretion in Chronic Fatigue Syndrome,
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215W. M. Jefferies, “Mild Adrenocortical Deficiency, Chronic Allergies, Autoimmune Disorders
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216 M. Krisiloff, “Solving Urinary Problems,” Let’s Live, October 1997;100. (back to text)
217 M. Krisiloff; personal communication. (back to text)
218
T. D. Moon, L. Hagen, and D. M. Heisey, “Urinary Symptomatology in Younger Men,” Urology,
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219P. C. Albertsen, “Urologic ‘Nuisances’: How to Work Up and Relieve Men’s Symptoms,”
Geriatrics, February 1997;52(2):46–50. (back to text)
220M. L. Slattery and D. W. West, “Smoking, Alcohol, Coffee, Tea, Caffeine, and Theobromine:
Risk of Prostate Cancer in Utah (United States),” Cancer Causes and Control November
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221S. Tas, R. Lauwerys, and D. Lison, “Occupational Hazards for the Male Reproductive System,”
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222M. Cetinkaya, J. von Duszeln, W. Thiemann et al., “Organochlorine Pesticide Residues in Raw
and Roasted Coffee and Their Degradation during the Roasting Process,” Zeitschrift fur
Lebensmittel Untersuchung und Forschung, July 1984;179(1):5–8. (back to text)
223L. Friedman, M. A. Weinberger, T. M. Farber et al., “Testicular Atrophy and Impaired
Spermatogenesis in Rats Fed High Levels of the Methylxanthines Caffeine, Theobromine, or
Theophylline,” Journal of Environmental Pathology and Toxicology, January 1979:2(3) :687–706.
(back to text)
224A. R. Ezzat and Z. M. el-Gohary, “Hormonal and Histological Effects of Chronic Caffeine
Administration on the Pituitary-gonadal and Pituitary-adrenocortical Axes in Male Rabbits,”
Functional and Developmental Morphology, 1994;4(1):45–50. (back to text)
225G. Potashnik and A. Porath, “Dibromochloropropane (DBCP):A 17-year Reassessment of
Testicular Function and Reproductive Performance,” Journal of Occupational and Environmental
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226 Ibid. (back to text)
227D. S. Weathersbee, R. L. Ax, and J. R. Lodge, “Caffeine-mediated Changes of Sex Ratio in
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228
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Quality,” Journal of ‘Andrology, March 1997;18(2):194–202. (back to text)
229
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Human Reproduction, June 1996;11(6):1244–46. (back to text)
230
M. J. De Souza, J. C. Arce, L. S. Pescatello et al., “Gonadal Hormones and Semen Quality in
Male Runners: A Volume Threshold Effect of Endurance Training,” International Journal of Sports
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231
H. Kentenich, H. Schmiady, E. Radke et al., “The Male IVF Patient—Psychosomatic
Considerations,” Human Reproduction, June 1992;7 supplement 1:13–18. (back to text)
232P. T. Giblin, M. L. Poland, K. S. Moghissi et al., “Effects of Stress and Characteristic
Adaptability on Semen Quality in Healthy Men,” Fertility and Sterility, January 1988;49(1):127–32.
(back to text)
233K. K. Harrison, V. J. Callan, and J. R. Hennessey, “Stress and Semen Quality in an In Vitro
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234
K. D. Israel et al., “Serum Uric Acid in Carbohydrate Sensitive Adults,” Annals of Nutrition and
Metabolism, 1983;32:1078–81. (back to text)
235M. M. Callahan, R. S. Robertson, M. J. Arnaud et al., “Human Metabolism of [1-methyl-l4C]
and [2-14C] Caffeine after Oral Administration,” Drug Metabolism and Disposition, July
1982;10(4):417–23. (back to text)
236D. M. Grant, B. K. Tang, M. E. Campbell et al., “Effect of Allopurinol on Caffeine Disposition
in Man,” British Journal of Clinical Pharmacology, April 1986;21(4):454–58. (back to text)
237N. R. Scott, D. Stambuk, J. Chakraborty et al., “Caffeine Clearance and Biotransformation in
Patients with Chronic Liver Disease,” Clinical Science, April 1988;74(4):377–84. (back to text)
238R. H. Davis, “Does Caffeine Ingestion Affect Intraocular Pressure?” Ophthalmology, November
1989;96(11):1680–81. (back to text)
239 E. J. Higginbotham, H. A. Kilimanjaro, J. T Wilensky et al., “The Effect of Caffeine on
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240
B. Hinzpeter and M. Diestelhorst, “1, 3, 7-trimethylxanthine: Effects on Orcadian Aqueous
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241G. Duncan, R. A. Riach, M. R. Williams et al., “Calcium Mobilisation Modulates Growth of
Lens Cells,” Cell Calcium, January 1996;19(1):83–89. (back to text)
242K. Lofti and J. E. Grunwald, “The Effect of Caffeine on the Human Macular Circulation,”
Investigative Ophthalmology and Visual Science, November 1991; 32(12):3028–32. (back to text)
243 Guide to Macular Degeneration, [Link] (back to
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244J. Evans and R. Wormald, “Is the Incidence of Registrable Age-related Macular Degeneration
Increasing?” British Journal of Ophthalmology, January 1996;80(1):9–14. (back to text)
Chapter 6
1M. J. Arnaud, “Metabolism of Caffeine and Other Components of Coffee,” in S. Garattini (ed.),
Caffeine, Coffee & Health, (New York: Raven Press, 1993), pp. 43–95. (back to text)
2D. W. Yesair, “Human Disposition and Some Biochemical Aspects of Methylxan-thines,” in G. A.
Spiller, The Methylxanthine Beverages and Foods: Chemistry, Consumption and Health Effects
(New York: Liss, 1984). (back to text)
3L. Linde, “Mental Effects of Caffeine in Fatigued and Non-fatigued Female and Male Subjects,”
Ergonomics, May 1995;38(5):864–85. (back to text)
4 J. Ferri, “Under Pressure,” Tampa Tribune-Times, April 27, 1997, 1. (back to text)
5T. E. Seeman, B. S. McEwen, B. H. Singer et al., “Increase in Urinary Cortisol Excretion and
Memory Declines: MacArthur Studies of Successful Aging,” Journal of Clinical Endocrinology and
Metabolism, 1997;82:2458–65. (back to text)
6 J. Ferri, “Under Pressure.” (back to text)
7 A. Gramenzi and A. Gentile et al., “Association between Certain Foods and Risk of Acute
Myocardial Infarction in Women,” British Medical Journal, March 24, 1990;300(6727):771–73.
(back to text)
8 R. B. Williams, J. C. Barefoot, J. A. Blumenthal et al., “Psychosocial Correlates of Job Strain in a
Sample of Working Women,” Archives of General Psychiatry, June 1997;54(6):543–48. (back to
text)
9 M. B. Schenker, M. Eaton, R. Green et al., “Self-reported Stress and Reproductive Health of
Female Lawyers,” Journal of Occupational and Environmental Medicine, June 1997;39(6):556–68.
(back to text)
10M. E. Tucker, “Despite H. pylori, Stress Still a Factor in Ulcers,” Family Practice News,
1994;24(12):17. (back to text)
11
E. A. Bergman, L. K. Massey, K. J. Wise et al., “Effects of Dietary Caffeine on Renal Handling of
Minerals in Adult Women,” Life Sciences, 1990;47(6):557–64. (back to text)
12P. T. Packard and R. R. Recker, “CafFeine Does not Affect the Rate of Gain in Spine Bone in
Young Women,” Osteoporosis International, 1996;6(2):149–52. (back to text)
13
D. C. Bauet, W. S. Browner, J. A. Cauley et al., “Factors Associated with Appendicular Bone
Mass in Older Women: The Study of Osteoporotic Fractures Research Group,” Annals of ‘Internal
Medicine, May 1, 1993;118(9):657–65. (back to text)
14R. P. Heaney and R. R. Recker, “Effects of Nitrogen, Phosphorus, and Caffeine on Calcium
Balance in Women,” Journal of Laboratory and Clinical Medicine, January 1982;99(1):46–55.
(back to text)
15C. Krahe, R. Friedman, J. L. Gross, “Risk Factors for Decreased Bone Density in Pre-menopausal
Women,” Brazilian Journal of Medical and Biological Research, September 1997;30(9):106l–66.
(back to text)
16
S. S. Harris and B. Dawson-Hughes, “Caffeine and Bone Loss in Healthy Post-menopausal
Women,” American Journal of Clinical Nutrition, October 1994;60(4):573–78. (back to text)
17L. K. Massey, E. A. Bergman, K. J. Wise et al., “Interactions between Dietary Caffeine and
Calcium on Calcium and Bone Metabolism in Older Women,” Journal of the American College of
Nutrition, December 1994;13(6):592–96. (back to text)
18 D. P. Kiel, D. T. Felson, M. T. Hannan et al., “Caffeine and the Risk of Hip Fracture: The
Framingham Study,” American Journal of Epidemiology, October 1990;132(4):675–84. (back to
text)
19M. Hernandez-Avila, G. A. Colditz, M. J. Stampfei et al., “Caffeine, Moderate Alcohol Intake,
and Risk of Fractures of the Hip and Forearm in Middle-aged Women,” American Journal of
Clinical Nutrition, July 1991;54(1):157–63. (back to text)
20D. Michelson, C. Stratakis, L. Hill et al., “Bone Mineral Density in Women with Depression,”
New England Journal of Medicine, 1996;335:1176–81. (back to text)
21J. E. White, “Osteoporosis: Strategies for Prevention,” Nurse Practitioner, September
1986;11(9):36–46. (back to text)
22
C L. Deal, “Osteoporosis, Prevention, Diagnosis, and Management,” American Journal of
Medicine, January 27, 1997;102(1A):35S–39S. (back to text)
23 J. J. Anderson, P. Rondano, and A. Holmes, “Roles of Diet and Physical Activity in the
Prevention of Osteoporosis,” Scandinavian Journal of Rheumatology, 1996,103:65–74. (back to
text)
24
M. P. Faine, “Dietary Factors Related to Preservation of Oral and Skeletal Bone Mass in
Women,” Journal of Prosthetic Dentistry, January 1995;73(1):65–72. (back to text)
25V. W. Bunker, “The Role of Nutrition in Osteoporosis,” British Journal ofBiomedical Science,
September 1994;51(3):228–40. (back to text)
26W. G. Thompson, “Coffee: Brew or Bane?” American Journal of the Medical Sciences, July
1994;308(1):49–57. (back to text)
27T. Gillespy, 3d, and M. P. Gillespy, “Osteoporosis,” Radiology Clinics of North America, January
1991;29(1):77–84. (back to text)
28T. A. Morck, S. R. Lynch, and J. D. Cook, “Inhibition of Food Iron Absorption by Coffee,”
American Journal of Clinical Nutrition, 1983;37(3):416–20. (back to text)
29 L. Hallberg, “Iron,” in Present Knowledge in Nutrition, 5th ed. (Washington D.C.: The
Nutritional Foundation, 1984), pp. 459–78. Also E. M. Haymes, “Nutritional Concerns: Need for
Iron,” Medicine and Science in Sports and Exercise, 1987; supplement 19:S197–S200. (back to text)
30 G. B. Gabrielli and G. De Sandre, “ExcessiveTea Consumption Can Inhibit the Efficacy of Oral
Iron Treatment in Iron-deficiency Anemia,” Haematologica, November-December 1995;80(6):518–
20. (back to text)
31J. D. Cook, C. A. Finch, and N. J. Smith, “Evaluation of the Iron Status of a Population,” Blood,
1976;48:449–55. (back to text)
32T. H. Bothwell, R. W. Charlton et al., Iron Metabolism in Man (Oxford, England: Blackwell
Scientific Publications, 1979). (back to text)
33 I. G. Ances, J. Granados, and M. Baltazar, “Serum Ferritin as an Early Determinant of Decreased
Iron Stores in Pregnant Women,” Southern Medical Journal, May 1979;72(5):591–92. (back to text)
34 E: Kaneshige, “Serum Ferritin as an Assessment of Iron Stores and Other Hematologic
Parameters during Pregnancy,” Obstetrics and Gynecology, February 1981;57(2):238–42. (back to
text)
35J. Buolakka, “Serum Ferritin in the Evaluation of Iron Status in Young Healthy Women,” Acta
Obstetrica et Gynecologica Scandinavica, 1980; supplement 95:35–41. (back to text)
36G. H. Guyatt, C. Patterson, M. Ali et al., “Diagnosis of Iron-deficiency Anemia in the Elderly,”
American Journal of Medicine, March 1990;88(3):205–09. (back to text)
37G. H. Guyatt, A. D. Oxman, M. Ali et al., “Laboratory Diagnosis of Iron-deficiency Anemia: An
Overview,” Journal of General Internal Medicine, March–April 1992;7(2):145–53. (back to text)
38 J. Puolakka, O. Janne, A. Pakarinen et al., “Serum Ferritin in the Diagnosis of Anemia during
Pregnancy,” Acta Obstetrica et Gynecologica Scandinavica, 1980; supplement 95:57–63. (back to
text)
39S. Kiechl, J. Willeit, G. Egger et al., “Body Iron Stores and the Risk of Carotid Atherosclerosis:
Prospective Results from the Bruneck Study,” Circulation, November 18, 1997;96(10):3300–07.
(back to text)
40 A. B. Bruner, “Randomized Study of Cognitive Effects of Iron Supplementation in Non-anemic
Iron-deficient Adolescent Girls,” Lancet, 1996;348 (October 12), 992–96. (back to text)
41
A. M. Rossignol, “Caffeine-containing Beverages and Premenstrual Syndrome in Young
Women,” American Journal of Public Health, November 1985;75(11):1335–37. (back to text)
42A. M. Rossignol and H. Bonnlander, “Caffeine-containing Beverages, Total Fluid Consumption,
and Premenstrual Syndrome,” American Journal of Public Health, September 1990;80(9):1106–10.
(back to text)
43A. M. Rossignol, H. Bonnlander, L. Song et al., “Do Women with Premenstrual Symptoms Self-
medicate with Caffeine?” Epidemiology, November 1991;2(6):403–08. (back to text)
44J. F. Mortola, L. Girton, and S. S. Yen, “Depressive Episodes in Premenstrual Syndrome,”
American Journal of Obstetrics and Gynecology, December 1989;161(pt 1): 1682–87. (back to text)
45A. M. Rossignol, J. Y. Zhang, Y. Z. Chen et al., “Tea and Premenstrual Syndrome in the People’s
Republic of China,” American Journal of Public Health, January 1989;79(1):67–69. (back to text)
46S. London, W. Willett, C. Longcope et al., “Alcohol and Other Dietary Factors in Relation to
Serum Hormone Concentrations in Women at Climacteric,” American Journal of Clinical Nutrition,
January 1991;53(1):166–71. (back to text)
47R. L. Ferrini and E. Barrett-Connor, “Caffeine Intake and Endogenous Sex Steroid Levels in
Postmenopausal Women: The Rancho Bernardo Study,” American Journal of Epidemiology,
October 1, 1996;144(7):642–44. (back to text)
48G. Del Rio, R. Menozzi, G. Zizzo et al., “Increased Cardiovascular Response to Caffeine in
Perimenopausal Women Before and During Estrogen Therapy,” European Journal of
Endocrinology, November 1996;135(5)598–603. (back to text)
49M. A. Lucerno and W. W. McCloskey, “Alternatives to Estrogen for the Treatment of Hot
Flashes,” Annals ofPharmacotherapy, July 1997;31(7–8):915–17. (back to text)
50G. L. Clementz and J. W. Dailey, “Psychotropic Effects of Caffeine,” American Family
Physician, May 1988;37(5):167–72. (back to text)
51A. Breier, D. S. Charney, and G. R. Heninger, “Agoraphobia with Panic Attacks: Development,
Diagnostic Stability, and Course of Illness,” Archives of General Psychiatry, November
1986;43(11):1029–36. (back to text)
52F. W. Foote and F. W. Stewart, “Comparative Studies of Cancerous versus Non-cancerous
Breasts,” Annals of Surgery, 1945;121:197–222. (back to text)
53P. G. Brooks, S. Gart, A. J. Heldfond et al., “Measuring the Effect of Caffeine Restriction on
Fibrocystic Breast Disease: The Role of Graphic Stress Telethermometry as an Objective Monitor of
Disease,” Journal of Reproductive Medicine, June 1981;26(6):279–82. (back to text)
54M. C. Hindi-Alexander, M. A. Zielezny, N. Montes et al., “Theophylline and Fibrocystic Breast
Disease,” Journal of Allergy and Clinical Immunology, June 1985;75(6):709–15. (back to text)
55J. P. Minton and H. Abou-Issa, “Nonendocrine Theories of the Etiology of Benign Breast
Disease,” World Journal of Surgery, November 1989;13(6):680–84. (back to text)
56J. P. Minton, M. K. Foecking et al., “Response of Fibrocystic Disease to Caffeine Withdrawal and
Correlation of Cystic Nudeotides with Breast Disease,” American Journal of Obstetrics and
Gynecology, 1979;135:157–58. (back to text)
57L. C. Russell, “Caffeine Restriction as Initial Treatment for Breast Pain,” February
1989;14(2):36–37. (back to text)
58B. Bullough, M. Hindi-Alexander, and S. Fetouh, “Methylxanthines and Fibrocystic Breast
Disease: A Study of Correlations,” Nurse Practitioner, March 1990;15(3):36–38. (back to text)
59P. Modica, “The Coffee Craze and Your Health,” Medical Tribune News Service, June 25, 1997.
(back to text)
60S. J. London, J. L. Connolly, S. J. Schnitt et al., “A Prospective Study of Benign Breast Disease
and the Risk of Breast Cancer,” Journal of the American Medical Association, 1992;267(7):941–44.
(back to text)
61C. W. Welsch, “Caffeine and the Development of the Normal and Neoplastic Mammary Gland,”
Proceedings of the Society for Experimental and Biological Medicine, October 1994;207(1):1–12.
(back to text)
62T. E. Rohan and A. J. McMichael, “Methylxanthines and Breast Cancer,” International Journal of
Cancer, March 15, 1988;41(3):390–93. (back to text)
63C. K. Stanton and R. H. Gray, “Effects of Caffeine Consumption on Delayed Conception,”
American Journal of Epidemiology, December 15, 1995;142(12):1322–29. (back to text)
64A. Wilcox, C. Weinberg, and D. Baird, “CafFeinated Beverages and Decreased Fertility,” Lancet,
December 24–31, 1988;2(8626–8627):l453–56. (back to text)
65F. Bolumar, J. Olsen, M. Rebagliato et al., “Caffeine Intake and Delayed Conception: A European
Multicenter Study on Infertility and Subfecundity: European Study Group on Infertility
Subfecundity,” American Journal of Epidemiology, February 15, 1997;l45(4):324–34. (back to text)
66B. Watkinson and P. A. Fried, “Maternal Caffeine Use before, during and after Pregnancy and
Effects upon Offspring,” Neurobehavioral Toxicology Teratology, January-February 1985;7(1):9–
17. (back to text)
67P. S. Weathersbee, L. K. Olson, and T. R. Lodge, “Caffeine and Pregnancy. A Retrospective
Survey,” Postgraduate Medicine, 1977;62:64–69. (back to text)
68 E Dlugosz, K. Belanger, K. Hellenbrand ec al., “Maternal Caffeine Consumption and
Spontaneous Abortion: A Prospective Cohort Study,” Epidemiology, May 1996;7(3):250–55. (back
to text)
69C. Infante-Rivard, A. Fernandez, R. Gauthier et al., “Fetal Loss Associated with Caffeine Intake
before and during Pregnancy,” Journal of the American Medical Association,
1993;270(24):294CM3. (back to text)
70W. Srisuphan and M. B. Bracken, “Caffeine Consumption during Pregnancy and Association with
Late Spontaneous Abortion,” American Journal of Obstetrics and Gyne-cology, January
1986;154(l):14–20. (back to text)
71R. M. Gilbert, “Caffeine as a Drug of Abuse,” in R. J. Gibbins et al. (eds.), Research Advances in
Alcohol and Drug Problems, vol. 3 (New York: John Wiley & Sons), pp. 49–176. (back to text)
72U.S. Department of Health and Human Services Public Health Service, Food and Drug
Administration, Caffeine and Pregnancy (FDA) 81–1081. (back to text)
73A. Nehlig and G. Debry, “Effects of Coffee and Caffeine on Fertility, Reproduction, Lactation,
and Development: Review of Human and Animal Data,” Journal de Gyne-cologie, Obstetrique et
Biologie de la Reproduction, 1994;23(3):241–56. (back to text)
74W. J. Hueston, G. M. Eilers, D. E. King et al., “Common Questions Patients Ask during
Pregnancy,” American Family Physician, May 1, 1995;51 (6): 1465–70. (back to text)
75 T. R. Martin and M. B. Bracken, “The Association between Low Birth Weight and Caffeine
Consumption during Pregnancy,” American Journal of Epidemiology 1987:126:813–21. (back to
text)
76L. Fenster, B. Eskenazi, G. C. Windham et al., “Caffeine Consumption during Pregnancy and
Fetal Growth,” American Journal of ‘Public Health, 1991;81:458–61. (back to text)
77I. Fortier, S. Marcoux, and L. Beaulac-Baillargeon, “Relation of Caffeine Intake during
Pregnancy to Intrauterine Growth Retardation and Preterm Birth,” American Journal of
Epidemiology, 1993:137:931–40. (back to text)
78H. Vlajinao, R. R. Petrovic, J. M. Marinkovic et al., “Effect of Caffeine Intake during Pregnancy
on Birth Weight,” American Journal of Epidemiology, 1997:145:335–38. (back to text)
79H. Tanaka, K. Nakazawa, and M. Arima, “Effects of Maternal Caffeine Ingestion on the Perinatal
Cerebrum,” Biology of the Neonate, 1987;51(6):332–39. (back to text)
80R. Matsuoka, H. Uno, H. Tanaka et al., “Caffeine Induces Cardiac and Other Malformations in
the Rat,” American Journal of Medical Genetics, supplement, 1987:3:433–43. (back to text)
81M. J. Rossowska, W. Carvajal, F. Joseph, Jr., et al., “Postnatal Caffeine Effects on Copper, Zinc,
and Iron Concentrations in Mammary Gland, Milk, and Plasma of lactating Dams and Their
Offspring,” Annals of Nutrition and Metabolism, 1997;41(l):60–65. (back to text)
82A. Nehlig and G. Debry, “Potential Teratogenic and Neurodevelopmental Consequences of
Coffee and Caffeine Exposure: A Review of Human and Animal Data,” Neurotoxicology and
Teratology, November-December 1994;16(6):531–43. (back to text)
83J. D. McGowan, R. E. Altman, and W. P. Kanto, Jr., “Neonatal Withdrawal Symptoms after
Chronic Maternal Ingestion of Caffeine,” Southern Medical Journal, September 1988;81(9):1092–
94. (back to text)
84 J. T. Sullivan, “Caffeine Poisoning in an Infant,” Journal of Pediatrics, 1977:90:1022–23. (back
to text)
85 Caffeine May Contribute to Infant Deaths,” Los Angeles Times, January 28, 1998; A–10. (back to
text)
86L. J. Benincosa, K. Sagawa, L. K. Massey et al., “Effects of Acute Caffeine Ingestion and
Menopause on Sulfate Homeostasis in Women,” Life Science, September 8, 1995;57(16):l497–1505.
(back to text)
Chapter 7
1P. J. Rogers, N. J. Richardson, and N. A. Elliman, “Overnight Caffeine Abstinence and Negative
Reinforcement of Preference for Caffeine-Containing Drinks,” Psychopharmacology (Berlin),
August 1995;120(4):457–62. (back to text)
2B. G. Phillips-Bute and J. D. Lane, “Caffeine Withdrawal Symptoms Following Brief Caffeine
Deprivation,” Physiology and Behavior, December 31, 1997;63(1):35–39. (back to text)
3J. M. Peters, “Factors Affecting Caffeine Toxicity: A Review of the Literature,” Journal of
Clinical Pharmacology, 1967:7:131–41. (back to text)
4 R. M. Gilbert, “Caffeine as a Drug of Abuse,” in R. J. Gibbins et al. (eds.), Research Advances in
Alcohol and Drug Problems, vol. 3 (New York: John Wiley & Sons, 1976), pp. 49–176. (back to
text)
5N. J. Birkett and A. G. Logan, “Caffeine-containing Beverages and the Prevalence of
Hypertension,” Journal of Hypertension, 1988;6 (supplement 4):S620–S622. (back to text)
6 F. A. Holloway, R. C. Michaelis, and P. L. Huerta, “Caffeine-phenylethylamine Combinations
Mimic the Amphetamine Discriminative Cue,” Life Science, February 25, 1985;36(8):723–30. (back
to text)
7 S. M. Mueller, J. Muller, and S. M. Asdell, “Cerebral Hemorrhage Associated with
Phenylpropanolamine in Combination with Caffeine,” Stroke, January 1984; 15(1):119–23. (back to
text)
8R. C. Michaelis, F. A. Holloway, D. C. Bird et al., “Interactions between Stimulants: Effects on
DRL Performance and Lethality in Rats,” Pharmacology, Biochemistry and Behavior, 1987;27:299–
306. (back to text)
9 D. Delibovi, “Is Coffee Fattening?” Lear’s, July 1991;13(2):36. (back to text)
10 B. Livermore, “Caffeine Boosts Eating Disorders,” Health, June 1991;16. (back to text)
11T. W. Castonguay, “Glucorcorticoids as Modulators in the Control of Feeding,” Brain Research
Bulletin, September-October 1991;27(3–4):423–28. (back to text)
12FDA Issues Public Warning Against Ma Huang Product,” Food Labeling News, 1995;3(22):15
(back to text)
13General Accounting Office (GAO), “Better Regulation of Pesticide Exports and Pesticide
Residues in Imported Food is Essential.” CED-79–43, Washington, D.C., 1979, .pg11. (back to text)
14S. A. Hearne, Harvest of Unknowns: Pesticide Contamination in Imported Foods, Natural
Resources Defense Council, New York, 1984, Appendix V. (back to text)
15 Ibid. (back to text)
16 Ibid. (back to text)
17A. H. el Sebae, “Special Problems Experienced with Pesticide Use in Developing Countries,”
Regulatory Toxicobgy and Pharmacology, June 1993;17(3):287–91. (back to text)
18J. G. Machado-Neto, T. Matuo, and Y. K. Matuo, “Semiquantitative Evaluation of Dermal
Exposure to Granulated Insecticides in Coffee (Coffea arabica L.) Crop and Efficiency of Individual
Protective Equipment,” Bulletin on Environmental Contamination and Toxicology, December
1996;57(6):946–51. (back to text)
19D. B. Rama and K. Jaga, “Pesticide Exposure and Cholinesterase Levels among Farm Workers in
the Republic of South Africa,” Science of the Total Environment, July 29, 1992;122(3):315–19
(back to text)
20 L. Tangley, Science, November 22, 1996. (back to text)
21G. Monbiot, “Land Ownership and the Flight to Amazonia,” in M. Colchester and L. Lohmann
(eds.), The Struggle for Land and the Fate of the Forests (London: Zed Books, 1995), pp. 139–63.
(back to text)
Chapter 8
1C. Gerrans, “Soft Drinks Tend to Boost Dietary Aluminum Intake,” Medical Tribune,
1992;33(4):17. (back to text)
2I. Marci and M. Giannoni, “Effect of Some Low pH Soft Drinks on Enamel,” Pre-venzione
eAssistenza Dentale, November—December 1988;l4(6):10–14. (back to text)
3A. I. Ismail, B. A. Burt, and S. A. Eklund, “The Cariogenicity of Soft Drinks in the United
States,” Journal of the American Dental Association, August 1984;109(2):241–45. (back to text)
4M. McKinney, “People with Braces Advised to Cut Soda Consumption,” Medical Tribune News
Service, October 14, 1997. (back to text)
5S. Stellman and L. Garfinkel, “Short Report: Artificial Sweetener Use and Weight Changes among
Women,” Preventive Medicine, 1986;15:195–202. (back to text)
6 A. Liguori, J. R. Hughes, and A. H. Oliveto, “Caffeine Self-administration in Humans: Efficacy of
Cola Vehicle,” Experimental and Clinical Psychopharmacology, August 1997;5(3):286–94. (back to
text)
7 E. C. Strain, G. K. Mumford, K. Silverman et al., “Caffeine Dependence Syndrome; Evidence
from Case Histories and Experimental Evaluations,” Journal of the American Medical Association,
1994;272:1043–48. (back to text)
8R. H. Adamson and H. R. Roberts, “Caffeine Dependence Syndrome,” (Letter), Journal of the
American Medical Association, 1995;273(18):1418. (back to text)
9Council on Scientific Affairs, “Caffeine Labeling,” Journal of the American Medical Association,
1984;252(6):803–06. (back to text)
10P. M. Guenther, “Beverages in the Diets of American Teenagers,” Journal of the American
Dietetic Association, 1986;86:493. (back to text)
11D. M. Graham, “Caffeine: Its Identity, Dietary Sources, Intake, and Biological Effects,”
Sourcebook on Food and Nutrition (Chicago: Marquis Academic Media, 1980). (back to text)
12 C. Kawai, A. Wakabayashi, T. Matsumura et al., “Reappearance of Beriberi Heart Disease in
Japan: A Study of 23 Cases,” American Journal of Medicine, September 1980;69(3):383–86. (back
to text)
13 A. C. Looker, P. R. Dallman, M. D. Carroll et al., “Prevalence of Iron Deficiency in the United
States,” Journal of the American Medical Association, March 26, 1997;277(12):973—76. (back to
text)
14
M. M. Garriga and D. D. Metcalfe, “Aspaitame Intolerance,” Annals of Allergy, December 1988
—61 (pt 2):63–69. (back to text)
15B. J. Kaplan, J. McNicol, R. A. Conte et al., “Dietary Replacement in Preschool-aged
Hyperactive Boys,” Pediatrics, January 1989;823(1):7–17. (back to text)
16M. Maes, M. Vandewoude, C. Schotte et al., “The Decreased Availability of L-tryp-tophan in
Depressed Females: Clinical and Biological Correlates,” Progress in Neuro-Psy-chopharmacology
and Biological Psychiatry, 1990;14(6):903–19. (back to text)
17J. Tynjala, L. Kannas, and E. Levalahti, “Perceived Tiredness among Adolescents and Its
Association with Sleep Habits and Use of Psychoactive Substances,” Journal of Sleep Research,
September 1997;6(3):189–98. (back to text)
18W. S. Terry and B. Phifer, “Caffeine and Memory Performance on the AVLT,” Journal of Clinical
Psychology, November 1986;42(6):860–63. (back to text)
19 A. B. Bruner, “Randomized Study of Cognitive Effects of Iron Supplementation in Non-anemic
Iron-deficient Adolescent Girls,” Lancet, 1996;348 (October 12), 992–96. (back to text)
20 You Are What You Drink, Too,” Los Angeles Times, December 22, 1996, p. E-2. (back to text)
21Dietary Goals for the United States, Select Committee on Nutrition and Human Needs, United
States Senate. U.S. Government Printing Office, February V977, pp. 46–47. (back to text)
22 1996 Statistical Abstract of the United States. (back to text)
23M. L. Arbeit, T. A. Nicklas, G. C. Frank et al., “Caffeine Intakes of Children from a Biracial
Populacion: The Bogalusa Heart Study,” Journal ofthe American Dietetic Association, April
1988;88(4):466–71. (back to text)
24G. A. Bernstein, N. Walters, R. Crosby et al., “Caffeine Withdrawal and the Effect on Normal
Children,” in Scientific Proceedings 43rd Annual meeting of the American Academy of Child and
Adolescent Psychiatry, Philadelphia, Penn., 1997. (back to text)
25H. L. Abrams, Jr., “Caffeine: A Paradigm of Subliminal Cultural Drug Habituation,” Journal of
Applied Nutrition, 1976;28:33–40. (back to text)
26L. L. Palmer, “Early Childhood Caffeine and Sugar Habituation,” Journal of Orthomolecular
Psychiatry, 1977;6:248–50. (back to text)
27G. Wyshak and R. E. Frisch, “Carbonated Beverages, Dietary Calcium, the Dietary
Calcium/phosphorus Ratio, and Bone Fractures in Girls and Boys,” Journal of Adolescent Health,
May 1994;15(3):210–15. (back to text)
28H. H. Draper and R. R. Bell, “Nutrition and Osteoporosis,” in H. H. Draper, (ed.), Advances in
Nutrition Research, vol 2. (New York: Plenum Press, 1977). (back to text)
29L. K. Massey and M. M. Strang, “Soft Drink Consumption, Phosphorus Intake, and
Osteoporosis,” Journal of the American Dietetic Association, 1982;80:581–83. (back to text)
30 K. G. Dewey, M. E. Romero-Abal, J. Quan de Serrano et al., “A Randomized Intervention Study
of the Effects of Discontinuing Coffee Intake on Growth and Morbidity of Iron-deficient
Guatemalan Toddlers,” Journal of Nutrition, February 1997;127(2):306–13. (back to text)
31B. Bates, “The Scoop on Soda Pop: Carbonated Beverages No Threat to Bones,” Family Practice
News, April 1996; 1:49. (back to text)
32 American Family Physician, 1994;50(4):830. (back to text)
33 D. G. Simons-Morton, S. A. Hunsberger, L. Van Horn et al., “Nutrient Intake and Blood Pressure
in the Dietary Intervention Study in Children,” Hypertension, April 1997;29(4):930–36. (back to
text)
34H. Baker, O. Frank, S. Feingold et al., “Vitamins, Total Cholesterol, and Triglycerides in 642
New York City School Children,” American Journal of Clinical Nutrition, 1987;20(8):850–57.
(back to text)
35P. M. Guenther, “Beverages in the Diets of American Teenagers,” Journal of the American
Dietetic Association, 1986;86:493. (back to text)
36C. L. Hays, “Be True to Your Cola, Rah, Rah: Battle for Soft Drink Loyalties Moves to Public
Schools,” The New York Times, March 10, 1998, p. C1-4. (back to text)
37 Ibid. (back to text)
38 Ibid. (back to text)
39 “Sweet Deals for Women’s Sports,” Working Woman, vol. 20, issue 2, February 1995;14. (back to
text)
40 S. Elliott, “Boys and Girls Clubs in Project with Coke,” The New York Times, December 6, 1996,
p. D4. (back to text)
41D. Barboza, “More Hip, Higher Hop: Caffeinated Drinks Catering to Excitable Boys and Girls,”
The New York Times, Friday August 22, 1997, pp. C1’C5. (back to text)
42 Ibid. (back to text)
Chapter 9
1B. D. Page and C. F. Charbonneau, “Headspace Gas Chromatographic Determination of
Methylene Chloride in Decaffeinated Tea and Coffee, with Electrolytic Conductivity Detection,”
Journal of the Association of Official Analytical Chemists, July 1984;67(4):757–61. (back to text)
2E. Lynge, A. Anttila, and K. Hemminki, “Organic Solvents and Cancer,” Cancer Causes and
Control, May 1997;8(3):406–19. (back to text)
3R. G. Liteplo, G. W. Long, and M. E. Meek, “Relevance of Carcinogenicity Bioassays in Mice in
Assessing Potential Health Risks Associated with Exposute to Methylene Chloride,” Human and
Experimental Toxicology, February 1998;17(2):84–87. (back to text)
4 H. R. Superko, W. Bortz, Jr., P. T. Williams et al., “Caffeinated and Decaffeinated Coffee Effects
on Plasma Lipoprotein Cholesterol, Apolipoproteins, and Lipase Activity: A Controlled,
Randomized Trial,” American Journal of Clinical Nutrition, September 1991;54(3):599–605. (back
to text)
5H. N. Graham, “Tea: The Plant and Its Manufacture: Chemistry and Consumption of the
Beverage,” in G. A. Spiller (ed.), The Methrylxanthine Beverages and Foods: Chemistry,
Consumption and Health Effects (New York: Alan R. Liss, 1984), pp. 29–74. (back to text)
6C. Rice-Evans, “Plant Polyphenols: Free Radical Scavengers or Chain-breaking Antioxidants?”
Biochemical Society Symposia, 1995:61:103–16. (back to text)
7K. Okushio, N. Matsumotot, T. Kohri et al., “Absorption of Tea Catechins into Rat Portal Vein,”
Biological and Pharmaceutical Bulletin, February 1996;19(2):326–29. (back to text)
8Y. Yoshiki, T. Kahara, K. Okuba et al., “Mechanism of Catechin Chemiluminescence in the
Presence of Active Oxygen,” Journal of Bioluminescence and Chemiluminescence, May–June
1996;11(3):131–36. (back to text)
9G. C. Yen and H. Y. Chen, “Relationship between Antimutagenic Activity and Major Components
of Various Teas,” Mutagenesis, January 1996;11(1):37–41. (back to text)
10A. Constable, N. Varga, J. Richoz et al., “Antimutagenicity and Catechin Content of Soluable
Instant Teas,” Mutagenesis, March 1996;11(2):189–94. (back to text)
11K. Goto, S. Kanaya, andY. Hara, Proceedings of the International Symposium on Tea Science,
314 (Shizuoka, Japan); August 1991. (back to text)
12 Y. Hara, T. Matsuzaki, andT. Suzuki, Nippon Nogeikagaku Kaishi, 61;803(1987). (back to text)
13Y. Sagesaka-Mitane, M. Miwa, and S. Okada, “Platelet Aggregation Inhibitors in Hot Water
Extract of Green Tea,” Chemical and Pharmaceutical Bulletin, (Tokyo) March 1990;38(3):790–93.
(back to text)
14H. L. Gensler, B. N. Timmerman, S. Valcic et al., “Prevention of Photocarcinogenesis by Topical
Administration of Pure Epigallocatechin Gallate Isolated from Green Tea,” Nutrition and Cancer,
1996;26(3):325–35. (back to text)
15P. Simon, P. Charbonneau, B. Vaucel et al., “Iron-deficiency Anemia during Excessive
Consumption of Tea,” Nouvelle Presse Medkale, January 10, 1981;10(1):44. (back to text)
16S. Vimkesant, S. Nakornchai, K. Rungruangsak et al., “Food Habits Causing Thiamine
Deficiency in Humans,” Journal of Nutrition Science and Vitaminology, August 1976;22
supplement: 1–2. (back to text)
17R. S. Wang and C. Kies, “Niacin, Thiamin, Iron and Protein Status of Humans as Affected by the
Consumption of Tea (Camellia sinensis) Infusions,” Plant Foods and Human Nutrition, October
1991;41(4):337–53. (back to text)
18K. Imai and K. Nakachi, “Cross Sectional Study of Effect of Drinking Green Tea on
Cardiovascular and Liver Diseases,” British Medical Journal, 1995:310:693–96. (back to text)
19 Evaluation of the Carcinogenic Risk to Humans: Coffee, Tea, Mate, Methlyxanthines, and
Methylglyoxal.” International Agency for Research on Cancer Monograph, 1991; vol. 51. (back to
text)
20 I. Oguni et al., Japanese Journal of Nutrition, 47;31(1989). (back to text)
21Y. T. Gao, J. K. McLaughlin, W. J. Blot et al., “Reduced Risk of Esophageal Cancer Associated
with Green Tea Consumption,” Journal of the National Cancer Institute, June 1, 1994;86(11):855–
58. (back to text)
22E. Giovannucci, A. Ascherio, E. B. Rimm et al., “Intake of Carotenoids and Retinol in Relation to
Risk of Prostate Cancer,” Journal ofthe National Cancer Institute, December 6, 1995;87(23):1767–
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23L. Kohlmeier, K. G. Weterings, S. Steck et al., “Tea and Cancer Prevention: An Evaluation of the
Epidemiologic Literature,” Nutrition andCancer, 1997;27(1):1–13. (back to text)
24B. D. Page and C. F. Charbonneau, “Headspace Gas Chromatographic Determination of
Methylene Chloride in Decaffeinated Tea and Coffee with Electrolytic Conductivity Detection,”
Journal of the Association of Official Analytical Chemists, July 1984;67(4):757–6l. (back to text)
25“EIeutherococcus: Strategy of the Use and New Data,” Research Institute of Biological Testing of
Chemical Compounds. Academy of Medical-Sciences, Moscow, 1987. (back to text)
26H. J. Meyer, “Pharmacology of Kava,” in Ethnopharmacologic Search for Psychoactive Drugs,
D. H. Efron et al. (eds.), Public Health Service Publication no. 1645. Washington, D.C.: U.S.
Government Printing Office, 1967, 133–40. (back to text)
27 A. von Gadow, E. Joubert, and C. F. Hansmann, “Comparison of the Antioxidant Activity of
Rooibos Tea with Green, Oolong and Black Tea,” Food Chemistry, 1997;vol. 60:(1)73–77. (back to
text)
28 C. Rabe, J. A. Steenkamp, E. Joubert et al., “Phenolic Metabolites from Rooibos Tea (Aspalathus
linearis)” Phytochemistry, 1994; vol. 35:(6):1559–65. (back to text)
29 E. Joubert and D. Ferrera, “Antioxidants of Rooibos Tea—A Possible Explanation for Its Health
Promoting Properties?” South African Journal of Food Science and Nutrition, 1996:8:79–83. (back
to text)
30S. Stellman and L. Garfinkel, “Short Report: Artificial Sweetener Use and Weight Changes
among Women,” Prevention Medicine, 1986:15:195–202. (back to text)
Chapter 10
1H. Jaggy and E. Koch, “Chemistry and Biology of Alkylphenols From Ginkgo biloba L.”
Pharmazie, Octobet 1997;52(10):735–38. (back to text)
2J. Haase, P. Halama, and R. Horr, “Effectiveness of Brief Infusions with Ginkgo biloba Special
Extract EGb 761 in Dementia of the Vascular and Alzheimer Type,” Zeitschrift fur Gerontologie
and Geriatrie, July 1996;29:(4):302–09. (back to text)
3M. V. R. Apparao, K. Srinivasan, and R. T. L. Koteswara, “The Effect of Centella asiatica on the
General Mental Ability of Mentally Retarded Children,” Indian Journal of Psychiatry, 1977:19:54–
59. (back to text)
4K. Nalini et al., “Effect of Centella asiatica Fresh Leaf Aqueous Extract on Learning and Memory
and Biogenic Amine Turnover in Albino Rats,” Phytotherapia, 1992;63(3):232–37. (back to text)
5 “Caffeine Can Increase Brain Serotonin Levels,” Nutrition Reviews, October 1988;46(10):366–67.
(back to text)
6S. Foster, “Milk Thistle, Silybum marianum,” Botanical series no. 305, American Botanical
Council, Austin, Texas, 1991. (back to text)
7G. Palasciano et al., “The Effect of Silymarin on Plasma Levels of Malon-dialdehyde in Patients
Receiving Long Term Treatment with Psychotropic Drugs,” Current Therapeutic Research, May
1994;55(5):537–45. (back to text)
8 G. P. Littatru, S. Lippa, A. Oradei et al., “Coenzyme Q10: Blood Levels and Metabolic Demand,”
International Journal of Tissue Reactions, 1990;12(3):145–48. (back to text)
9 S. Fujimoto, N. Kurihara, K. Hirata et al., “Effects of Coenzyme Q10 Administration on
Pulmonary Function and Exercise Performance in Patients with Chronic Lung Diseases,” Clinical
Investigation, 1993;71(8 supplement):S162–S166. (back to text)
10 W. J. Koroshetz, B. G. Jenkins, B. R. Rosen et al., “Energy Metabolism Defects in Huntingtons
Disease and Effects of Coenzyme Q10,” Annals of Neurology, February 1997;41(2):160–65. (back
to text)
11R. Lodi, R. Rinaldi, A. Gaddi et al., “Brain and Skeletal Muscle Bioenergetic Failure in Familial
Hypobetalipoproteinaemia,” Journal of Neurology, Neurosurgery and Psychiatry, June
1997;62(6):574–80. (back to text)
12M. Mizuno, B. Quistorff, H. Theorell et al., “Effects of Oral Supplementation of Coenzyme Q10
on 31P-NMR Detected Skeletal Muscle Energy Metabolism in Middle-aged Post-polio Subjects and
Normal Volunteers,” Molecular Aspects of Medicine, 1997;18 supplement:S291–S298. (back to text)
13 M. Kamei and T. Fujita et al., “The Distribution and Content of Ubiquinone in Foods,”
International Journal for Vitamin and Nutrition Research, 1986;56:57. (back to text)
14G. Lenaz, R. Fato, G. Castelluccio et al., “An Updating of the Biochemical Function of
Coenzyme Q in Mitochondria,” Molecular Aspects of Medicine, 1994,15 supplement:S29–S36.
(back to text)
15D. A. Porter, D. L. Costill, J. J. Zachwieja et al., “The Effect of Oral Coenzyme Q10 on the
Exercise Tolerance of Middle-aged, Untrained Men,” International Journal of Sports Medicine,
October 1995;16(7):421–27. (back to text)
16
J. Karlsson, L. Lin, C. Sylven et al., “Muscle Ubiquinone in Healthy Physically Active Males,”
Molecular and Cellular Biochemistry, March 23, 1996;156(2):169–72. (back to text)
17C. Marconi, G. Sassi, and P. Cerretelli, “The Effect of an Alpha-Ketoglutarate-Pyridoxine
Complex on Human Maximal Aerobic and Anaerobic Performance,” European Journal of Applied
Physiology, 1982;49(3):307–17. (back to text)
18A. L. Goldberg and T. W. Chang, “Regulation and Significance of Amino Acid Metabolism in
Skeletal Muscle,” Federation Proceedings, 1978;37:2301–07. (back to text)
19R. P. Shank and D. J. Bennett, “2-Oxoglutarate Transport: A Potential Mechanism for Regulating
Glutamate and Tricarboxylic Acid Cycle Intermediates in Neurons,” Neurochemical Research, April
1993;18(4):401–10. (back to text)
20G. E. Karandashova, E. M. Kruptiskii, V. N. Petrov et al., “Study of Gamma-aminohutyric Acid
(GABA) Concentration in Blood Plasma of Alcoholism Patients,” Voprosy Meditsinskoi Khimii,
March–April 1993;39(2):36–37. (back to text)
21 A. E. Morgan and S. L. Dewey, “Effects of Pharmacologic Increases in Brain GABA Levels on
Cocaine-induced Changes in Extracellular Dopamine,” Synapse, January 1998;28(1):60–65. (back
to text)
22T. Kaneko and N. Mizuno, “Glutamate-synthesizing Enzymes in GABAergic Neurons of the
Neocortex, A Double Immunofluorescence Study in the Rat,” Neuroscience, August
1994;61(4):839–49. (back to text)
23 C. Marconi, “The Effect of an Alpha-Ketoglutarate-Pyridoxine Complex.” (back to text)
24 M. H. Williams, “Vitamin Supplementation and Athletic Performance,” International Journal for
Vitamin and Nutrition Research, 1989;30:163–91. (back to text)
25 B. Chrisley and J. Driskell, “Vitamin B-6 Status of Adults in Virginia,” Nutrition Reports
International, 1979:19:553–60. (back to text)
26H. Gutherie and A Crocetti, “Implications of a Protein-based Standard for Vitamin B-6,”
1983;28:133–38. (back to text)
27A. Stewart, “Clinical and Biochemical Effects of Nutritional Supplementation on the
Premenstrual Syndrome,” Journal of Reproductive Medicine, 1987;32(6):345–41. (back to text)
28R. L. Rizek and K. S. Tippett, “Diets of American Women: 1977 & 1985,” Bulletin of the
Michigan Dental Hygiene Association, 1989;19(2):3–6. (back to text)
29 K. Suboticanec et al., “Effects of Pyridoxine and Riboflavin Supplementation on Physical Fitness
in Young Adolescents,” International Journal for Vitamin and Nutrition Research, 1990;60(10):81–
88. (back to text)
30W. Bunker, M. M. Lawson et al., “The Uptake and Excretion of Chromium by the Elderly,”
American Journal of ‘Clinical Nutrition, 1984;39:799–802. (back to text)
31P. Koivistoinen, “Mineral Element Composition of Finnish Foods,” Ada Agricultura
Scandinavica, 1980; supplement, 22. (back to text)
32 R. A. Anderson and A. S. Kozlovsky, “Chromium Intake, Absorption and Excretion of Subjects
Consuming Self-selected Diets,” American Journal of Clinical Nutrition, 1984;41:1177–83. (back to
text)
33 R. Riales and M. J. Albrink, “Effect of Chromium Chloride Supplementation on Glucose
Toletance and Serum Lipids Including High Density Lipoprotein of Adult men,” American Journal
of Clinical Nutrition, 1981;34:2670–78. (back to text)
34R. A. Anderson, M. M. Polansky et al., “Chromium Supplementation of Human Subjects: Effects
on Glucose, Insulin and Lipid Parameters,” Metabolism, 1983;32:894–99. (back to text)
35R. A. Anderson, M. M. Polansky et al., “Effects of Supplemental Chromium on Patients with
Reactive Hypoglycemia,” Metabolism, 1987;36:351–55. (back to text)
36
W. H. Glinsmann and W. Mertz, “Effect ofTrivalent Chromium on Glucose Tolerance,”
Metabolism: Clinical and Experimental, 1966;15:510. (back to text)
37R. A. Anderson, M. M. Polansky et al., “Effects of Chromium Supplementation on Insulin,
Insulin Binding and C-peptide Values of Hypoglycemic Human Subjects,” American Journal of
Clinical Nutrition, 1985;41:841. (back to text)
38J. Clausen, “Chromium Induced Clinical Improvement in Symptomatic Hypoglycemia,”
Biological Trace Element Research, 1988;17:229–36. (back to text)
39
J. T. Hicks, “Treatment of Fatigue in General Practice: A Double Blind Study,” Clinical
Medicine, 1964;71:85–90. (back to text)
40
D. L. Shaw et al., “Management of Fatigue, A Physiological Approach,” American Journal of
Medical Science, 1962;243:98–109, 758–69. (back to text)
41I. Franz and H. Paradies, “Potassium-magnesium Aspartate as a Positive Homotropic Effector,”
Arzneim Forsch, 1979;29:1676–80. (back to text)
42V. Tyler, The Honest Herbal, 3rd ed. (New York: Pharmaceutical Product Press, 1993), p. 155.
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43I. Wiklund, J. Karlberg, and B. Lund, “Improved Quality of Life with Ginseng Preparations?
Positive Effects in Healthy Working People,” Lakartidningen, September 6, 1995;92(36):3196–
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44 K. A. Wesnes, R. A. Faleni, N. R. Hefting et al., “The Cognitive, Subjective, and Physical Effects
of a Ginkgo bibbalVunax Ginseng Combination in Healthy Volunteers with Neurasthenic
Complaints,” Psychopharmacology Bulletin, 1997;33(4):677–83. (back to text)
45T. K. Yun and S. Y. Choi, “Preventive Effect of Ginseng Intake Against Various Human Cancers:
A Case-control Study on 1987 Pairs,” Cancer Epidemiology, Biomarkers and Prevention, June
1995;4(4):401–08. (back to text)
46X. Chen, S. Salwinski, and T. J. Lee, “Extracts of Ginkgo biloba and Ginsenosides Exert Cerebral
Vasorelaxation via a Nitric Oxide Pathway,” Clinical and Experimental Pharmacology and
Physiology, December 1997;24(12):958–59. (back to text)
47Eleutherococcus: Strategy of the Use and New Data, Research Institute of Biological Testing of
Chemical Compounds, Academy of Medical Sciences, Moscow, 1987. (back to text)
48Pharmacology and Application of Chinese Materia Medica, Chinese Medicinal Material
Research Center, Chinese University of Hong Kong, 1984. (back to text)
49Y. Y. Cui and M. Z. Wang, “Aspects of Schizandrin Metabolism In Vitro and In Vivo,” European
Journal of Drug Metabolism and Pharmacokinetics, April–June 1993;18(2):155–60. (back to text)
50L. Zhang and X. Niu, “Effects of Schizandrol A on Monoamine Neurotransmicters in the Central
Nervous System,” Acta Academiae Medkinae Sinicae, February 1991;13(1):13–16. (back to text)
51P. Laukkanen, E. Heikkinen, M. Schroll et al., “A Comparative Study of Factors Related to
Carrying Out Physical Activities of Daily Living (PADL) among 75-Year-Old-Men and Women in
Two Nordic Localities,” Aging, August 1997;9(4):258–67. (back to text)
52M. P. van Boxtel, F. G. Paas, P. J. Houx et al., “Aerobic Capacity and Cognitive Performance in a
Cross-sectional Aging Study,” Medicine and Science in Sports and Exercise, October
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53M. S. Albert, K. Jones, G. R. Savage et al., “Predictors of Cognitive Change in Older Persons:
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54R. Manber, R. R. Bootzin, C. Acebo et al., “The Effects of Regularizing Sleep-wake Schedules on
Daytime Sleepiness,” Sleep, June 1996;19(5):432–41. (back to text)
55H. J. Meyer, “Pharmacology of Kava,” in Ethnopharmacologic Search for Psychoactive Drugs,
D. H. Efron et al. (eds.), Public Health Service Publication no. 1645. Washington, D.C.: U.S.
Government Printing Office, 1967:133–40. (back to text)
56E. Lehmann, E. Kiszler, and J. Friedemann, “Efficacy of a Special Kava Extract (Piper
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19. (back to text)
Conclusion
1C. Cohen, W. B. Pickworth, E. B. Bunker et al., “Caffeine Antagonizes EEG Effects of Tobacco
Withdrawal,” Pharmacology, Biochemistry and Behavior, April 1994;47(4):919–36. (back to text)
THEY SAY Caffeine gives you energy…
THEY SAY Caffeine gives you a lift…
THEY SAY Caffeine sharpens your mind…
DON’T BELIEVE THE JAVA JIVE!
Nearly 80 percent of all Americans—even doctors and
journalist—are hooked on caffeine, this country’s #1
addiction. A natural component of coffee, tea, and chocolate—
and added to drugs, soft drinks, candy, and many other
products, this powerful drug can affect brain function,
hormone balance, and sleep patterns, while increasing your
risk of osteoporosis, diabetes, ulcers, PMS, stroke, heart
disease, and certain types of cancer.
Now for the first time, one of the most accomplished
nutritional biochemists and medical writers in his field reveals
the truth about caffeine and helps you kick the habit forever.
DISCOVER:
• A step-by-step, clinically proven program that
reduces your caffeine intake without the headaches,
fatigue, and depression associated with withdrawal
• Effective ways to boost your energy with a group of
newly discovered nutrients, healthy beverages, better
sleep, and high-energy habits
• A fabulous new life of vibrant health, vitality, and
mental clarity.
1 * Although chocolate does not contain a great deal of
caffeine, it contains high amounts of a related compound
known as theobromine. If you add the stimulant effects of both
caffeine and theobromine, chocolate has the stimulating power
of forty milligrams of caffeine per one-ounce piece. (back to
text)
Reducing caffeine intake is suggested for improved health outcomes due to various negative effects on the body. Caffeine is linked with increased blood pressure, reduced bone density, osteoporosis, and anxiety disorders . High caffeine consumption increases calcium loss, which can lead to osteoporosis, particularly in women who consume more than two or three servings of coffee per day . Furthermore, caffeine contributes to stress and tension, which can exacerbate anxiety and panic disorders . A trial period without caffeine can lead to significant health benefits, such as improved calcium levels, reduced anxiety, and generally better physical and emotional health . The Off the Bean program described in Source 5 suggests a gradual withdrawal from caffeine to minimize withdrawal symptoms and maximize health improvements .
Caffeine dependency can lead to both physiological and psychological effects. Physiologically, caffeine affects the heart, causing arrhythmias such as palpitations and ventricular beats, which can be particularly dangerous for individuals with mitral valve prolapse or blocked arteries . It can also act as a mutagen, damaging DNA and hampering DNA repair, thereby contributing to aging and potential cancer risks . Moreover, caffeine can cause a "crash" after its initial stimulating effects wear off, leading to fatigue and adrenal exhaustion . Psychologically, caffeine may exacerbate anxiety, depression, and panic attacks, and chronic use can result in a condition known as caffeinism, characterized by irritability, nervousness, and sleep disturbances . Additionally, caffeine has been linked to decreased mental acuity and memory recall, despite initial perceptions of increased alertness .
Caffeine plays a significant role in stress-related physical health issues by disrupting emotional resilience and amplifying responses to stressors. Caffeine consumption lowers the threshold for stress tolerance, leading to anxiety, irritability, and anger, which can escalate normal stress reactions into significant emotional disturbances . High caffeine intakes are associated with increased levels of stress hormones such as epinephrine and norepinephrine, which elevate heart rate and blood pressure, triggering fight-or-flight responses even in non-threatening situations . Over time, this persistent stimulation contributes to the deterioration of physical health, as these stress hormones can lead to chronic health issues, including hypertension and cardiovascular diseases . Additionally, caffeine withdrawal and its effects on mental health, such as depression and anxiety, further compound stress-related disorders .
The interaction between caffeine, diet, and cancer risk presents an inconclusive and complex picture. For example, while some studies suggest that caffeine may be associated with certain cancer risks, such as prostate cancer among men consuming high levels of theobromine, a compound related to caffeine , other studies do not find a consistent link between caffeine and cancer, including breast cancer . Studies on tea, which contains caffeine, show mixed cancer risk results—some suggest benefits, particularly with green tea consumption, but these benefits don't consistently apply to those who consume alcohol or smoke . Overall, while caffeine is often included in discussions of diet and cancer risk, the current research does not definitively establish caffeine as a significant factor in cancer risk reduction or increase . Thus, a balanced diet rich in antioxidants and a reduction in saturated fats may provide a more reliable approach to reducing cancer risk ."}
Alternatives for caffeine consumption include caffeine-free beverages that can be satisfying and healthful, as suggested by pioneers in caffeine-free drink development like Caroline MacDougall . These alternatives purportedly improve health by contributing to better sleep, reducing the risk of anxiety and panic attacks, and decreasing headaches . Additionally, reducing or eliminating caffeine intake has been associated with improved mood, enhanced energy levels, decreased reliance on other drugs, and overall improved health . These benefits arise from eliminating the cycle of anxiety, depression, and impaired sleep commonly linked to caffeine consumption ."}
Caffeine consumption appears to have a complex relationship with cardiovascular health. While some sources claim that normal levels of caffeine intake (200 to 300 mg per day) do not pose a significant health hazard, the content suggests that caffeine can elevate stress hormones and thus increase cardiovascular stress, potentially leading to increased risk for heart attack and stroke . Habitual caffeine consumption does not seem to provide immunity against these effects; in fact, caffeine can exacerbate cardiovascular issues, especially when combined with stress or in those with pre-existing hypertension . Furthermore, caffeine’s effects do not always habituate, meaning regular users can still experience increased blood pressure from caffeine . Overall, caffeine may contribute to cardiovascular stress and associated risks, suggesting caution in its consumption, particularly in vulnerable populations.
The document suggests that caffeine negatively impacts mental clarity and cognitive function. It creates a roller-coaster effect of mental clarity alternating with confusion, depression, and lethargy, and impairs memory and cognition . Caffeine gives an illusion of heightened alertness by causing chemical stimulation rather than genuinely increasing mental activity, leading ultimately to mood letdowns, depression, and chronic fatigue . Additionally, caffeine causes uncontrolled neuron firing, creating a stressed state that disrupts brain function . Overall, caffeine is portrayed as impairing rather than enhancing cognitive function and mental clarity.
Green tea contains approximately twenty-five milligrams of caffeine per cup, whereas black tea typically has sixty to ninety milligrams per six-ounce cup brewed for five minutes, making black tea higher in caffeine content . Green tea is often considered to have potential health benefits, such as reducing cancer risk, but these claims are stronger compared to black tea, which may be associated with increased cancer risks for certain types . Green tea also has a higher percentage of catechins, powerful antioxidants with various health benefits, whereas black tea has a much lower catechin content . Therefore, while both teas offer benefits from polyphenols, green tea is generally seen as more beneficial due to its lower caffeine content and higher antioxidant levels .
Caffeine withdrawal should be managed by gradually decreasing caffeine intake while incorporating health-promoting habits to mitigate withdrawal effects such as splitting headaches, fatigue, depression, and brain fog . A gradual reduction avoids a sudden increase in brain blood flow, which can cause severe headaches, the most common withdrawal symptom due to blood vessel dilation . Additional support through nutritional and herbal methods can help rebuild mental vitality and restore natural energy production, reducing fatigue and depression . Avoiding abrupt cessation is crucial to prevent the cycle of dependency, as sudden withdrawal from caffeine often exacerbates symptoms like headache and depression, which are widespread among caffeine users . Medication containing caffeine should be avoided as it may relieve withdrawal headaches momentarily but can perpetuate dependency and increase headache frequency over time .