--> By Gloria Dulan-Wilson
This is another in a series of health tips that I do from time to time - particularly when I lose a friend or a loved one - such as Theresa Freeman, and my Aunt Vivian who died within one day of each other - or because I've come across some important information that I know that we don't know about yet in the Black community.
It's vital that we stay as healthy as we possibly can. And I'm not saying it's easy. I've had and am having my challenges too. But prayer alone is not going to do the trick. I've got some dear ones in my family I've already sent this to. I'll share part of the cover letter I sent with you without revealing who it was addressed to. Needless to say we can't allow them or us to be prey to doctors who only know how to push pill. We have to do our homework and make sure we know as much as possible about what it is they're giving us, the benefits and the side effects as well.
And any bozo doctor who tells you that vitamins are bad for you - including nursing mothers - kick him or her to curb quickly. I have six friends with high blood pressure who were put on cumodin and warfarin - both are rat poisons - and these same doctors warned them against vitamins!! Really!
This is a compilation of information from Life Extension Magazine. Of course I also mention my favorite Dr. Scott Greenberg - but he has his plate pretty full these days. Just make sure your physician is a holistic doctor who knows about food and nutrition as well as pharmaceuticals.
Hope this helps you all!
This is a follow up to the information I gave you over the phone - in addition to the vitamin D3, which is the minimal amount for helping your High Blood pressure. There are several other supplements that you need to be taking, and some things that are recommended that you eliminate from your diet as well.Life Extension has been around for forty years now, and is the foremost authority of healthy living because they don't just study Western medicine, but what other countries and cultures are doing effectively to stay healthy and to cure diseases.We DULANS are a strong people - so I know you can absorb this and begin to make sure that your doctors make the changes or make them yourself. You don't need to be on long term meds that don't promote health. Besides, OBAMACARE STATES CATEGORICALLY that if the procedure hasn't healed the problem withing a proscribed period of time, either the doctor is not doing it right, or the procedure is no good, or the medicine is ineffective. You have a right to demand to be healthy.stay blessed &HEALTHY &ECLECTICALLY BLACKGLORIAOH YES, YOU MIGHT WANT TO START SUBSCRIBING TO LIFE EXTENSION MAGAZINE - AND ALSO PIPE SOME SOOTHING, MEDITATING MUSIC INTO YOUR ROOMS AT HOME - IF YOU DON'T HAVE ANY, I'LL SEND YOU SOME LINKS. LUV4U -
- Reduce Blood Pressure—Naturally
What Americans Can Learn from Traditional Cultures about Managing HypertensionBy William Davis, MD
High blood pressure is a pervasive and devastating health threat to the aging population. If you’re an American adult, the chances you suffer from it are 1 in 3. If you’re over 60, that number rises to 1 in 2.1
There’s also a good chance you don’t know you have it. Approximately 30% of aging individuals remain unaware they suffer from hypertension.2 It is often called the “silent killer” for this reason—chronic high blood pressure is a reliable risk factor for heart attacks, heart failure, strokes, aneurysms, and kidney failure.3 Even modest increases in blood pressure can have serious consequences: every 20/10 mmHg increment over 115/75 mmHg doubles your risk of cardiovascular disease.4
In conventional medicine, the most your doctor might do to help you correct hypertension is tell you to lose weight, cut your salt intake, and follow a diet program like DASH (Dietary Approaches to Stop Hypertension). Prescription drugs typically follow. A DASH approach of avoiding salty and fried foods, and eating more nuts, vegetables, and fruits can indeed reduce blood pressure modestly (5.5 mmHg systolic, 3.0 mmHg diastolic, compared to a control diet similar to a standard American diet).5
What your doctor won’t tell you is that while hypertension tends to rise with age in our culture, it is not necessarily an inherent part of the aging process. On the contrary: our knowledge of the relationship between diet and health in other cultures offers compelling evidence that high blood pressure can often be controlled without drugs.
This article describes how my patients have been able to attain optimal blood pressure with a few simple changes in how they eat, how they live, and the nutrients they ingest.
An “Inevitable” Health Problem?Why are traditional cultures spared from high blood pressure while modern Americans suffer from epidemic high blood pressure—almost inevitably?
The current guidelines for hypertension management are detailed in the Seventh Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC 7), last updated in 2003. In JNC 7, normal blood pressure is defined as less than 120/80 mmHg; pre-hypertension is classified as between 120-139/80-89 mmHg. High blood pressure is classified as stage I (140-159/90-99 mmHg) or stage II (greater than 160/100 mmHg).4
Yet the Yanomamo and Xingu Indians of Brazil, rural Kenyans and natives of Papua, New Guinea, have blood pressures that typically average 103/63 mmHg!1 Even with aging, members of these cultures fail to develop the “expected” age-related increase in blood pressure that we are so accustomed to seeing.
Early studies exploring the reasons why traditional peoples have lower blood pressure focused principally on sodium/salt intake. But factors beyond salt have emerged, including higher potassium intake, less alcohol intake, and especially lower body weight.2,3 We can also safely extrapolate that people like the Yanomamo don’t eat chips, crackers, fruit drinks, or the thousands of other processed foods that we consume in excess. Are there lessons to be learned from traditional cultures that might help us avoid the otherwise inevitable high blood pressure that we experience in the modern world?
Four Nutritional Approaches
Nutrition plays a critical role in determining blood pressure. In traditional societies, the inclusion of abundant plant-sourced foods and wild game, along with exclusion of processed foods and food additives like high-fructose corn syrup, confer extraordinary lifelong protection from hypertension. This diet is a far cry from the misguided low-fat notions that are partly responsible for the American obesity and diabetes crisis. While the low-fat theme dominated American nutritional advice in the past, focusing only on restricting the quantity of fat intake may be detrimental. Rather, it may be more important to focus on the types of fats in the diet. For instance, it is crucial to replace saturated and hydrogenated fats with unsaturated and omega-3 fats in order to help reduce heart disease risk.15
Over the past 50 years, the American food industry has created a destructive and extraordinarily far-reaching array of industrial foods. The average American diet of processed carbohydrates like breakfast cereals and breads (all low-fat!), trans/hydrogenated fatty acids, high-fructose corn syrup, and overly-sugared foods is a guaranteed path towards high blood pressure, not to mention cholesterol distortions, increased inflammatory responses, and obesity.16,17
While the DASH diet achieves a reduction of several mmHg in blood pressure,5 you can take the diet several steps further for greater benefit. One potent means of reducing blood pressure is to mimic the lifestyle of traditional cultures and eliminate modern industrial foods that contribute to hypertension, while increasing the foods that reduce blood pressure. Since hunting wild game or foraging for cassava root and wild berries is not an option for most people, the goal is to simulate a modern version of a “traditional” lifestyle.
Such important dietary changes include:
Elimination of wheat and cornstarchThis strategy, as unexpected as it might be to many people, is probably the most potent strategy we have employed in our heart disease prevention and reversal clinic. It is not uncommon in our clinic to see blood pressure reductions of 20-40 mmHg, along with reduction or elimination of the “need” for blood pressure-reducing medication, not to mention dramatic weight loss, correction of cholesterol distortions (reduction in triglycerides, increased HDL, decreased LDL), and reduced inflammation.
Wheat is a particular problem in the American diet. A large number of Americans suffer from undiagnosed allergy or sensitivity to wheat. An additional, smaller number suffer from a devastating condition called celiac disease. People with celiac disease experience severe intestinal inflammation and destruction when exposed to gluten (a protein found in wheat and other grains such as rye and barley). Celiac survivors (“survivors” because celiac disease is a potentially fatal illness) who recover from this devastating intestinal illness by eliminating gluten tend to achieve a healthier body mass index than the wheat-consuming public. One study showed that patients with celiac disease who avoid gluten were more slender, since they take in 13-14% fewer calories than the general public (consistent with removal of the appetite-stimulating effect of wheat products).18 Another study found that wheat avoidance helped patients with celiac disease achieve a healthier weight—those who were underweight gained weight, while those who were overweight lost weight.19 Celiac patients who avoid gluten also benefit from higher HDL and ApoA1 levels.20
In our experience, elimination or dramatic reduction of wheat (white and whole grain breads, pasta, breakfast cereals, bagels, muffins, pretzels, crackers, pancakes, waffles) and cornstarch (cornmeal, tacos, tortillas, wraps, chips, breakfast cereals, gravies), as well as obvious sugary foods like candies, fruit juices, and fruit drinks, can serve as a powerful cornerstone of a blood pressure-reducing program if an individual has celiac disease or is allergic to wheat.
Many people are reluctant to follow a wheat-free program, since wheat is so commonplace in the American diet. I often advise skeptical patients to try a 4-week long “experiment”: eliminate wheat, as well as cornstarch and sugars, and see what happens. With rare exceptions, the effects are nothing short of extraordinary.
What You Need to Know: Reduce Blood Pressure
- It is estimated that 1 in 3 American adults and half of those over 60 years old suffer from hypertension. It is a reliable risk factor for heart attacks, heart failure, strokes, aneurysms, and kidney failure.
- While traditional cultures rarely suffer the health dangers of high blood pressure (hypertension), the condition has become increasingly widespread in modern society.
- Every 20/10 mmHg increase in blood pressure over the level 115/75 mmHg doubles cardiovascular risk.
- Doctors typically first recommend implementing the low-sodium DASH diet to combat hypertension.
- First-line prescription treatment for hypertension consists of thiazide diuretics, which can adversely alter lipid profiles and increase the risk of metabolic syndrome.
- Clinical experience suggests that dietary modifications, including eliminating dietary wheat and unhealthy oils, may promote healthy blood pressure.
- Certain foods and nutrients may help promote healthy blood pressure. These include nuts, vitamin D, magnesium, coenzyme Q10, French maritime pine bark extract, anthocyanins, magnesium, omega-3 fats, resveratrol, acetyl-L-carnitine, and melatonin.
Elimination of “trans” and hydrogenated fatsThe proliferation of “trans” or hydrogenated fats was among the many nutritional mistakes made in the misguided low-fat era. Hydrogenated vegetable shortening, followed by margarines and countless processed foods, increased Americans’ intake of “trans” fats dramatically.21 It increased the risk of heart attack, cancer, diabetes, and high blood pressure with it.22,23 Elimination of “trans” fats is therefore a crucial step in gaining control over blood pressure.
Eliminate “trans” fats simply by examining the label: if it lists hydrogenated or partially hydrogenated oils, don’t buy it. Even better, buy foods that don’t require a label, like cucumbers and tomatoes.
Elimination of oxidized oils
Oxidation of oils by heating leads to blood pressure-increasing effects, not to mention oxidative changes in cholesterol particles and cancer induction.24-26 Polyunsaturated oils, like corn and safflower, are the most susceptible to oxidative degradation and should therefore be minimized.26,27 Any heating, especially deep-frying, will oxidize oils. Oils are best consumed unheated, especially polyphenol- and tocotrienol-rich olive and flaxseed oil, since these nutrients are degraded by heat.27,28
Weighing your diet heavily in favor of blood pressure-reducing foodsWeighing your diet in favor of real foods rich in flavonoids and polyphenols, non-wheat fibers, and healthy oils is important for gaining control over blood pressure. It is just as important to choose foods that don’t overstimulate insulin release: processed foods like wheat products, cornstarch-containing products, and sugars.
Chief among foods that help reduce blood pressure are: raw nuts (almonds, walnuts, pecans, Brazil nuts, hazelnuts, pistachios; raw is crucial, since most roasted nuts have been roasted in blood pressure-increasing hydrogenated oils) and seeds (pumpkin, sunflower); vegetables; berries (blueberries, strawberries, cranberries, cherries, blackberries, elderberries); and healthy oils (olive, flaxseed, avocado, coconut).29
Supplements for Optimal Blood Pressure ManagementBeyond changing your diet to minimize exposure to foods that increase blood pressure and emphasizing foods that reduce blood pressure, a number of nutritional supplements have been confidently demonstrated to reduce blood pressure. Several supplements, including vitamin D, magnesium, omega-3 fatty acids from fish oil, and anthocyanins, correct inadequate intakes of these nutrients that commonly occur with modern lifestyles. Restoring them allows us to mimic the nutrient intakes of traditional cultures. Other supplements exert unique blood pressure-reducing effects independent of correcting nutritional deficiencies.
Vitamin DBlood pressure reduction is one of the many extraordinary health benefits of vitamin D.
People deficient in vitamin D are more likely to have high blood pressure.48,49 Vitamin D supplementation, alone or with calcium, can reduce blood pressure in people with hypertension.50,51 Vitamin D likely exerts this effect in part by suppressing the expression of the blood pressure hormone renin, similar to the effect of prescription angiotensin-converting enzyme (ACE) inhibitors.52
In our clinic, we dose vitamin D by checking blood levels of 25-hydroxyvitamin D and maintaining this measure between 60-70 ng/mL; the average dose requirement to do so is 6,000 units per day—far more than the now woefully outdated Recommended Adequate Intake for adults over age 50 of 400 IU/day. Because individual requirements vary widely, however, it is advisable to have blood levels checked on occasion to ensure the desired level has been achieved, neither too high nor too low.
Coenzyme Q10Among antioxidants, coenzyme Q10 (CoQ10) stands out for its ability to promote healthy blood pressure levels.
Pooled data from 12 studies (362 participants) revealed an impressive drop of 16.6 mg Hg in systolic pressure, and an 8.2 mm drop in diastolic pressure with CoQ10 doses ranging from 30-360 mg per day.53
Recent reports suggest that reducing blood pressure may not be enough to eliminate risk for cardiovascular complications like death and heart attack. Reduction of abnormal heart muscle thickening, or “hypertrophy” (measured by ultrasound), may also be a necessary component of treatment.54 CoQ10 has been shown to reduce abnormal hypertrophy resulting from high blood pressure.55,56 All of this is accomplished with virtually no side effects, given the fact that CoQ10 occurs naturally in the human body.
Thiazide Diuretics: A First-line Mistake
Thiazide diuretics, such as hydrochlorothiazide and chlorthalidone, are first-line drugs usually prescribed to treat hypertension, as advised by the JNC 7.4 They are inexpensive, have proven efficacy for reducing blood pressure, and physicians are well-acquainted with their use. But are they safe?
First of all, we all recognize the health benefits of good hydration, including restoring energy and cognitive performance, and prevention of blood clotting and kidney stones.6-8
Then why are dehydrating agents like thiazide diuretics prescribed? Diuretics work by reducing the volume of fluid in the body and in blood vessels, thus lowering pressure. (Ask anyone who has taken a diuretic: the loss of fluid (i.e., as urine)can be quite astounding.) But you can’t have both adequate hydration and dehydration—you’ve got to pick one or the other.
Thiazide diuretics have a number of undesirable effects, including:
These are not unexpected side effects that occur in a few; they are expected effects that develop in a substantial proportion.13
- Reduction of protective high-density lipoprotein (HDL)9
- Increased triglycerides10
- Increased total cholesterol9
- Increased insulin resistance and diabetes risk11
- Increased uric acid, which may increase the risk of a gout attack12
In one large study, 7.7% of those taking thiazide-type diuretics developed diabetes over the course of 4 years, compared with only 4.2-4.7% of patients taking other types of prescription diuretics.14
Although thiazides are widely prescribed as the first choice for hypertension, this class of drugs is fraught with a range of significant undesirable side effects.
French Maritime Bark ExtractNumerous studies point to the efficacy of a novel antioxidant compound of proanthocyanidins and bioflavonoids isolated from bark of the French maritime pine that grows along the southern coast of France.
A University of Arizona study documented 50% reduced need for blood pressure medication in diabetic participants taking 125 mg of this compound per day.57 Interestingly, there was a 23.7 mg/dL drop in blood sugar and 0.8% reduction in hemoglobin A1c (a measure of long-term blood sugar control). Another study demonstrated reduced need for calcium blocker medication in participants given 100 mg per day.58
French maritime bark extract exerts its antihypertensive effects by blocking the angiotensin-converting enzyme (ACE)—similar to the mechanism of the prescription ACE inhibitors enalapril and lisinopril—enhancing endothelial (vessel lining) responsiveness, and blocking the effects of adrenaline (epinephrine).59
AnthocyaninsAnthocyanins are a class of plant flavonoids that confer the red, purple, and blue color to cranberries, blueberries, eggplant, grapes, red wine, pomegranate, and other similarly colored fruits and vegetables. Anthocyanins are proving to be powerful standouts for health effects among the many thousands of flavonoids and polyphenols identified to date.
A Finnish study of 72 middle-aged subjects examined the effects of consuming two servings of berries daily (alternating schedule of 100 g whole bilberries and a 50 g crushed lingonberry nectar; or black currant or strawberry purée and cold-pressed chokeberry and raspberry juice) compared to a non-berry containing calorie-matched control. Anthocyanins represented the dominant flavonoid at 275 mg of the total polyphenols of 837 mg per day. The berry group experienced a reduction in systolic blood pressure of 7.3 mmHg, along with 5.2% increase in HDL.60 A study of 50 mL (almost 2 oz) of anthocyanin-rich pomegranate juice reduced blood pressure by about 12%, in addition to reducing carotid intima-media thickness.61
Like French maritime bark extract and vitamin D, anthocyanins are natural inhibitors of the angiotensin-converting enzyme that increases blood pressure.62 The production of the natural and powerful artery-relaxing agent, nitric oxide, is also increased by anthocyanins.63
Some of the richest sources of anthocyanins are elderberries, chokeberries, and bilberries, which are difficult to find in the US, but may be obtained as nutritional supplements and extracts.
An Everyday Dietary Danger
What food can cause devastating inflammatory intestinal destruction that, if unrecognized, can lead to disability and death?18
Increase blood sugar higher and faster than table sugar?30
Trigger autoimmune inflammation in the thyroid?31
Create intestinal bloating, cramps, and alternating diarrhea and constipation, often labeled irritable bowel syndrome?32
Weaken the muscle controlling food exit from the esophagus to the stomach, resulting in reflux esophagitis (heartburn)?33
Worsen schizophrenia in susceptible individuals?34
Contribute to behavioral outbursts in children with autism?35,36
Increase the risk of or worsen various inflammatory diseases such as rheumatoid arthritis, ulcerative colitis, dermatitis herpetiformis, systemic lupus, pancreatitis, and increase measures of inflammation? 37-42
Cause unexplained anemia, mood swings, fatigue, fibromyalgia, eczema, and osteoporosis?38,43-45
That food is wheat. Yes, the ubiquitous grain we are urged to eat more and more by the USDA, the American Heart Association, the American Dietetic Association, and the American Diabetes Association. Wheat is among the most destructive ingredients in the modern diet, worse than sugar, worse than high-fructose corn syrup, worse than any fat. What other common food can result in such an extensive list of diseases, even death?
Few foods occupy the exalted position that wheat has gained, earning over 20,000 research publications in the medical literature over the past 30 years, many studies detailing the destructive and sometimes fatal nature of this common dietary product. Celiac disease alone affects more than 2 million Americans.46 The medical literature is filled with case reports of deaths from this disease,47 often after years of struggle with incapacitating intestinal dysfunction and encephalopathy (brain inflammation).
What happens when you remove wheat from the diet? Experience at our clinic has shown that the majority of people quickly shed 20-30 lbs in the first few weeks, selectively lost from the abdomen (what I call “wheat belly”); blood sugar plummets; triglycerides drop up to several hundred milligrams, HDL increases, LDL drops (yes, wheat elimination is a means of achieving marked reduction in LDL, especially the small, heart disease-causing variety); and C-reactive protein plummets. In addition, intestinal complaints like pain, gas, and bloating improve or disappear; gastroesophageal reflux often disappears; rashes improve; inflammatory conditions like rheumatoid arthritis improve; diabetes (adult or type 2) is more easily controlled; and behavioral disorders and mood improve.
In people who have celiac disease, the meticulous avoidance of wheat gluten and gluten from other sources, including rye, spelt, and barley, will be necessary. But there are millions of Americans who are suffering wheat-intolerance in some form, from skin rashes to arthritis to depression, who are wheat-sensitive but remain unaware.
Beware of the food industry’s efforts to capitalize on wheat intolerance with products known as “gluten free.” These are generally foods that don’t trigger the inflammatory response of wheat, but still cause high blood sugar, weight gain, and other abnormalities.
MagnesiumIn addition to magnesium’s capacity to help manage asthma attacks, migraine headaches, eclampsia and pre-eclampsia of pregnancy, heart rhythm disorders, and preserve kidney function,64,65 magnesium supplementation has been conclusively shown to reduce blood pressure.66 Magnesium deficiency contributes an even larger blood pressure-increasing effect in the setting of a modern American diet deficient in magnesium and rich in fructose—a situation that increases inflammation and the potential for metabolic syndrome.67
In one recent study, magnesium supplementation reduced systolic blood pressure by 5.6 mmHg and diastolic blood pressure by 2.8 mmHg.68 People with heart disease may derive even greater effects. A study of 50 participants with advanced heart disease demonstrated a 9.0 mmHg drop in systolic pressure with 500 mg elemental magnesium supplementation, despite serum magnesium levels in the normal range.69
The blood pressure-reducing effects of magnesium supplementation may be especially marked in those with low serum magnesium levels. A study of supplementation in diabetic participants starting with low serum magnesium levels demonstrated an astounding 20.4 mmHg drop in systolic blood pressure and an 8.7 mmHg drop in diastolic pressure with 450 mg of elemental magnesium daily.70
Omega-3 Fatty AcidsIn addition to the triglyceride- and cardiovascular event-reducing effects of omega-3 fatty acids from fish oil, these fascinating oils also modestly reduce blood pressure. Daily intake of 1,000-3,000 mg of the omega-3 fatty acids EPA and DHA reduces systolic blood pressure by about 2.1 mmHg and diastolic pressure by about 1.6 mmHg.71 These blood pressure-reducing effects are accomplished via blocking the angiotensin system, promoting arterial relaxation (normalization of endothelial dysfunction), reduced production of inflammatory mediators, and reduced production of artery constricting factors.72
ResveratrolRed wine in modest quantities has been demonstrated to reduce risk for cardiovascular disease.73 Much attention has focused on the polyphenol resveratrol, originating from red wine and grapes as a principal source of benefits, including potential life-extending effects due to activation of the sirtuin genes.74
Resveratrol has been shown to inhibit the angiotensin-converting enzyme as a means to modestly reduce blood pressure,75 and also restores production of the natural artery-dilating agent, nitric oxide.76,77
Acetyl-L-carnitineIn a preliminary study, this amino acid reduced systolic blood pressure 9 mmHg in subjects taking 1,000 mg twice per day.78 In addition, acetyl-L-carnitine improved insulin responses and reduced blood sugar.
MelatoninBecause nocturnal hypertension has been associated with increased risk for cardiovascular events,79 the effect of melatonin on nighttime hypertension has been studied.
In addition to its sleep-enhancing effects, melatonin taken at or before bedtime reduces blood pressure during sleep. One study examined the effects of nightly dosing of 2.5 mg in 16 men; melatonin reduced systolic and diastolic blood pressure during sleep by 6 and 4 mmHg, respectively.80 Another study of 38 men demonstrated that 2 mg of a controlled-release melatonin preparation reduced systolic pressure by 6 mmHg and diastolic pressure by 3 mmHg during sleep.81
SummaryThe virtual absence of hypertension in traditional cultures suggests that high blood pressure is, for most of us, a situation we create with modern diet and lifestyle. Reverting back to basic foods, especially reducing or eliminating wheat grains, cornstarch, and sugars, can reduce blood pressure substantially. Select nutrients, many of which restore nutrients that were more readily obtained by traditional eating habits but are lacking in the modern day diet, can also reduce blood pressure. While not everyone starting such a program during adulthood can hope to entirely avoid hypertension, these steps might help minimize the potential of developing this dangerous condition.
If you have any questions on the scientific content of this article, please call a Life Extension® Health Advisor at 1-866-864-3027.
Dr. William Davis campaigns for the cause of heart disease reversal. He practices cardiology in Milwaukee, Wisconsin and is author of the book, Track Your Plaque (iUniverse, Inc., 2004). Dr. Davis can be contacted through www.trackyourplaque.com.
Editor’s NoteIn this article, Dr. Davis has provided us with an abundance of natural methods to lower blood pressure.
As Dr. Davis noted in the introduction, even modest blood pressure readings above 115/75 sharply increase cardiovascular disease risk. Yet conventional doctors are allowing their aging patient’s blood pressure to reach dangerous levels of 140/90 before initiating anti-hypertensive therapy.
In fact, the home page of a pharmaceutical company’s web site (www.diovan.com) defines high blood pressure as 140/90 or higher.
This drug company is acting against its own economic interest by limiting the number of people who are candidates for its anti-hypertensive drug, while disseminating erroneous lethal information to the public.
We urge most Life Extension members to maintain their blood pressure at 115/75 (or lower) using natural methods first. If blood pressure remains stubbornly high, we suggest a safe and effective class of anti-hypertensive drugs be used called angiotensin II receptor antagonists. One of these drugs we have recommended for over a decade is called Cozaar® and it should be taken twice a day to maintain 24-hour control over blood pressure. Another drug in this class called Benicar® claims 24-hour blood pressure control with once a day dosing.
You should not trust any medication to provide 24-hour blood pressure control. If you are prescribed Benicar® or any other anti-hypertensive, use an at-home blood pressure monitoring device to make sure the drug is providing all-day control of blood pressure at the optimal range of 115/75 or lower. A major error in using anti-hypertensive drugs is that they wear off later in the day allowing blood pressure to spike to dangerously high levels.
You can obtain reliable at-home blood pressure monitors at your local pharmacy, or you can order one by phone by calling 1-800-544-4440.
Epidemic Deficiency of Vitamin E
By William Faloon
If people had to rely on the news media for accurate health information, they might be influenced into making some very poor decisions.
by William Faloon
For instance, new studies about vitamin E are published every week. The findings from virtually all of these studies, however, remain buried in scientific journals—that is, unless there is an unfavorable outcome. Since vitamin E is a popular supplement, the media turns negative results into headline news stories, thus leading Americans to believe that they do not need supplemental vitamin E.
Life Extension has analyzed the negative studies about vitamin E and exposed the many flaws in them. The major problem with these studies is that older test subjects (who are in poor health to begin with) are given alpha-tocopherol by itself. It is hard to imagine that alpha-tocopherol in isolation could reverse a lifetime of free-radical tissue damage, yet these are the kinds of studies the media has used to vilify vitamin E.1-9
Largest Study on Vitamin E OverlookedOn November 10, 2006, the largest study in medical history was published using blood levels of alpha-tocopherol as the marker of vitamin E status in male smokers.10 The purpose of this study was to correlate baseline vitamin E levels with specific causes of death and overall mortality over a 19-year period. There were 29,000 subjects initially enrolled and 13,000 deaths available for analysis.
The study results showed a significant reduction in overall mortality in those with the highest blood levels of alpha-tocopherol. When looking at specific diseases, men with the highest blood levels of alpha-tocopherol showed the following reductions in causes of death over the 19-year study period:
Despite the enormous size of this study, and the fact that it was published in a major scientific journal, the media all but ignored these remarkable findings.
Disease Mortality Reduction Prostate cancer 32% Ischemic stroke 37% Hemorrhagic stroke 35% Lung cancer 21% Respiratory illness 42%
How Vitamin E Protected These Men Against DiseaseWhen discussing the biological mechanisms by which alpha-tocopherol reduced mortality across this wide spectrum of diseases, the scientists who conducted this study stated:
“As a primary fat-soluble antioxidant that protects lipids from peroxidation, alpha-tocopherol is able to scavenge mutagenic free radicals and inhibit the oxidation of LDL cholesterol, and these abilities have important implications for the prevention of carcinogenesis and atherosclerosis. . . alpha-tocopherol also has several important functions that are independent of its antioxidant activity, including modulation of gene expression, enhancements of immune responses, and suppression of tumor angiogenesis.”10
In describing why the study findings were so positive, the scientists noted that unlike in certain previous studies, test subjects with the higher alpha-tocopherol levels also displayed more beneficial gamma-tocopherol in their blood. The scientists elaborated that when alpha-tocopherol (vitamin E) is taken alone, it can deplete the body of gamma-tocopherol and antagonize the effects of vitamin K.10-15
A large body of published research documents the critical importance of gamma-tocopherol, especially when high doses of alpha-tocopherol are also taken.16-31 Researchers are finally recognizing what Life Extension members learned long ago—that is, the critical importance of following a program that includes both alpha- and gamma-tocopherol, along with vitamin K.
“Gamma-tocopherol is a powerful scavenger of reactive nitrogen oxide species and an inhibitor of the cyclooygenase-2 enzyme.”10
—American Journal of Clinical Nutrition - November 10, 2006, page 1206
In their concluding remarks, the scientists who conducted this most recent study stated:
“Our findings support a more robust role for circulating alpha-tocopherol in overall, cancer, and cardiovascular mortality than was suggested by previous studies.” 10
Shocking Deficiencies of Vitamin EThe editorial that accompanied this study revealed that 93% of American men and 96% of American women do not consume the recommended dietary allowance of vitamin E. Based on these startling statistics, the editorial questioned why doctors ever advocated that vitamin E supplements should be avoided!32,33
The editorial went on state the importance of establishing the amount of vitamin E necessary to “reduce the risk of chronic diseases,” rather than the minimal amount needed to “prevent a deficiency symptom.”
By analyzing fine details of the study, the editorial clearly demonstrated that the amount of vitamin E needed to achieve the optimal results shown in this study could be achieved “only with supplements.”
As was so adroitly pointed out by the editors, the federal government says Americans need only 12 milligrams a day of vitamin E, yet even this minute amount is not found in the diets of 93% of men and 96% of women in the United States,32 ergo the need for most Americans to take supplemental vitamin E.
“It is striking that the authors report that the men in the highest quintile of baseline serum concentrations of alpha-tocopherol had significantly lower risks of total and cause-specific mortality, including cardiovascular disease and cancer, than did the men in the lowest quintile of baseline serum concentrations of alpha-tocopherol.” 32
—Editorial - American Journal of Clinical Nutrition - November 10, 2006, page 959
Don’t Be a Victim of Drug Company PropagandaIt is in the economic interests of drug companies to steer Americans away from healthier lifestyles and dietary supplements. As more Americans fall ill to degenerative disease, drug company profits increase exponentially.
Enormous amounts of pharmaceutical dollars are spent influencing Congress, the FDA, and other federal agencies. The result is the promulgation of policies that cause Americans to be deprived of effective, low-cost means of protecting themselves against age-related disease.
The fact that the diets of more than 90% of Americans supply less than the 12 milligrams a day of vitamin E the government proclaims to be adequate is a startling revelation. It documents an epidemic deficiency of vitamin E among Americans who do not take supplements. Despite these grim statistics, the medical establishment continues to question the value of supplemental vitamin E.
As a member of the Life Extension Foundation, you gain access to scientific knowledge that could protect you against a host of common diseases—information that is too often distorted by the government and ignored by the mainstream media.
For longer life,
References .. References 1. Carvalho JJ, Baruzzi RG, Howard PF, et al. Blood pressure in four remote populations in the INTERSALT Study. Hypertension. 1989 Sep;14(3):238-46.
2. Ahmed MI, Pisoni R, Calhoun DA. Current options for the treatment of resistant hypertension. Expert Rev Cardiovasc Ther. 2009 Nov;7(11):1385-93.
3. Geleijnse JM, Witteman JC, Bak AA, den Breeijen JH, Grobbee DE. Reduction in blood pressure with a low sodium, high potassium, high magnesium salt in older subjects with mild to moderate hypertension. BMJ. 1994 Aug 13;309(6952):436-40.
4. The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. JAMA. 2003 May 21;289(1):2560-75.
5. Appel L J, Moore T J, Obarzanek E, et al. A clinical trial of the effects of dietary patterns on blood pressure. DASH Collaborative Research Group. N Engl J Med. 1997 Apr 17;336(16):1117–24.
6. Szinnai G, Schachinger H, Arnaud MJ, Linder L, Keller U Effect of water deprivation on cognitive-motor performance in healthy men and women. Am J Physiol Regul Integ Comp Physiol. 2005 Jul;289(1):R275-80.
7. Colussi G, De Ferrari ME, Brunati C, Civati G. Medical prevention and treatment of urinary stones. J Nephrol. 2000 Nov-Dec;13 Suppl 3:S65-70.
8. Pastorova VE, Esartiia DT. Status of the coagulant and anticoagulant systems of the blood in experimental acute intestinal dehydration of the body. Biull Eksp Biol Med. 1981 Sep;92(9):287-9.
9. Bagdade JD, Buchanan WF, Pollare T, Lithell H. Effects of hydrochlorothiazide and captopril on lipoprotein lipid composition in patients with essential hypertension. Eur J Clin Pharmacol. 1996;49(5):355-9.
10. Nandeesha H, Pavithran P, Madanmohan T. Effect of antihypertensive therapy on serum lipids in newly diagnosed essential hypertensive men. Angiology. 2009 Apr-May;60(2):217-20.
11. Haffner SM. The prediabetic problem: development of non-insulin-dependent diabetes mellitus and related abnormalities. J Diabetes Complications. 1997 Mar-Apr;11(2):69-76.
12. Reungjui S, Pratipanawatr T, Johnson RJ, Nakagawa T. Do thiazides worsen metabolic syndrome and renal disease? The pivotal roles for hyperuricemia and hypokalemia. Curr Opin Nephrol Hypertens. 2008 Sep;17(5):470-6.
13. Zillich AJ, Garg J, Basu S, et al. Thiazide diuretics, potassium, and the development of diabetes: a quantitative review. Hypertension. 2006 Aug;48(2):219-24.
14. Black HR, Davis B, Barzilay J, et al. Metabolic and clinical outcomes in nondiabetic individuals with the metabolic syndrome assigned to chlorthalidone, amlodipine, or lisinopril as initial treatment for hypertension: a report from the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT). Diabetes Care. 2008 Feb;31(2):353-60.
15. Hu FB, Manson JE, Willett WC. Types of dietary fat and risk of coronary heart disease: a critical review. J Am Coll Nutr. 2001 Feb;20(1):5-19.
16. Elliott SS, Keim NL, Stern JS, Teff K, Havel PJ. Fructose, weight gain, and the insulin resistance syndrome. Am J Clin Nutr. 2002 Nov;76(5):911-22.
17. Matía Martín P, Lecumberri Pascual E, Calle Pascual AL. Nutrition and metabolic syndrome. Rev Esp Salud Publica. 2007 Sep-Oct;81(5):489-505.
18. Bardella MT, Fredella C, Prampolini, L et al. Body composition and dietary intakes in adult celiac disease patients consuming a strict gluten-free diet. Am J Clin Nutr. 2000 Oct;72(4):937-39.
19. Cheng J, Brar PS, Lee AR, Green PH. Body mass index in celiac disease: beneficial effect of a gluten-free diet. J Clin Gastroenterol 2009 Sep 23.
20. Capristo E, Malandrino N, Farnetti S, et al. Increased serum high-density lipoprotein-cholesterol concentration in celiac disease after gluten-free diet treatment correlates with body fat stores. J Clin Gastroenterol. 2009 Nov-Dec;43(10):946-9.
21. Rizek RL, Friend B, Page L. Fat in today’s food supplylevel of use and sources. J Am Oil Chem Soc. 1974;51:244-50.
22. Astrup A, Dyerberg J, Selleck M, Stender S. Nutrition transition and its relationship to the development of obesity and related chronic diseases. Obes Rev. 2008 Mar;9 Suppl 1:48-52.
23. Chavarro JE, Stampfer MJ, Campos H, Kurth T, Willett WC, Ma J. A prospective study of trans-fatty acid levels in blood and risk of prostate cancer. Cancer Epidemiol Biomarkers Prev. 2008 Jan;17(1):95-101.
24. Rohr-Udilova NV, Stolze K, Sagmeister S, Nohl H, Schulte-Hermann R, Grasl-Kraupp B. Lipid hydroperoxides from processed dietary oils enhance growth of hepatocarcinoma cells. Mol Nutr Food Res. 2008 Mar;52(3):352-9.
25. Adam SK, Das S, Soelaiman IN, Umar NA, Jaarin K. Consumption of repeatedly heated soy oil increases the serum parameters related to atherosclerosis in ovariectomized rats. Tohoku J Exp Med. 2008 Jul;215(3):219-26.
26. Soriquer F, Rojo-Martínez G, Dobarganes MC, et al. Hypertension is related to the degradation of dietary frying oils. Am J Clin Nutr. 2003 Dec;78(6):1092-97.
27. Bozan B, Temelli F. Chemical composition and oxidative stability of flax, safflower and poppy seed and seed oils. Bioresour Technol. 2008 Sep;99(14):6354-9.
28. Brenes M, García A, Dobarganes MC, Velasco J, Romero C. Influence of thermal treatments simulating cooking processes on the polyphenol content in virgin olive oil. J Agric Food Chem. 2002 Oct 9;50(21):5962-7.
29. Babio N, Bulló M, Salas-Salvadó J. Mediterranean diet and metabolic syndrome: the evidence. Public Health Nutr. 2009 Sep;12(9A):1607-17.
30. Available at: http://lpi.oregonstate.edu/
infocenter/foods/grains/gigl. html. Accessed December 9, 2009.
31. Rousset H. A great imitator for the allergologist: intolerance to gluten. Eur Ann Allergy Clin Immunol. 2004 Mar;36(3):96-100.
32. Verdu EF, Armstrong D, Murray JA, et al. Between celiac disease and irritable bowel syndrome: the “no man’s land” of gluten sensitivity. Am J Gastroenterol. 2009 Jun;104(6):1587-94.
33. Cuomo A, Romano M, Rocco A, et al. Reflux oesophagitis in adult coeliac disease: beneficial effect of a gluten free diet. Gut. 2003 Apr;52(4):514-17.
34. Kalaydjian AE, Eaton W, Cascella N, Fasano A. The gluten connection: the association between schizophrenia and celiac disease. Acta Psychiatr Scand. 2006 Feb;113(2):82-90.
35. Vojdani A, O’Bryan T, Green JA et al. Immune response to dietary proteins, gliadin and cerebellar peptides in children with autism. Nutr Neurosci. 2004 Jun;7(3):151-61.
36. Elder JH, Shankar M, Shuster J, Theriaque D, Burns S, Sherrill L. The gluten-free, casein-free diet in autism: results of a preliminary double blind clinical trial. J Autism Dev Disord. 2006 Apr;36(3):413-20.
37. Collin P, Reunala T, Pukkala E, et al. Coeliac disease--associated disorders and survival. Gut. 1994 Sep;35(9):1215-18.
38. Hernandez L, Green PH. Extraintestinal manifestations of celiac disease. Curr Gastroenterol Rep. 2006 Oct;8(5):383-89.
39. Volta U, De Angelis GL, Granito A, et al. Autoimmune enteropathy and rheumatoid arthritis: a new association in the field of autoimmunity. Dig Liver Dis. 2006 Dec;38(12):926-9.
40. Freeman HJ. Adult celiac disease followed by onset of systemic lupus erythematosus. J Clin Gastroenterol. 2008 Mar;42(3):252-5.
41. Rodrigo L, Alvarez N, Riestra S, et al. Relapsing acute pancreatitis associated with gluten enteropathy. Clinical, laboratory, and evolutive characteristics in thirty-four patients. Rev Esp Enferm Dig. 2008 Dec;100(12):746-51.
42. Festen EA, Szperl AM, Weersma RK, Wijmenga C, Wapenaar MC. Inflammatory bowel disease and celiac disease: overlaps in the pathology and genetics, and their potential drug targets. Endocr Metab Immune Disord Drug Targets. 2009 Jun;9(2):199-218.
43. McGough N, Cummings JH. Coeliac disease: a diverse clinical syndrome caused by intolerance of wheat, barley and rye. Proc Nutr Soc. 2005 Nov;64(4):434-50.
44. Wallace DJ, Hallegua DS. Fibromyalgia: the gastrointestinal link. Curr Pain Headache Rep. 2004 Oct;8(5):364-8.
45. Prigent F, Civatte J. Atopy and associated diseases. Ann Dermatol Venereol. 1982;109(4):341-53.
46. Available at: http://digestive.niddk.nih.
gov/ddiseases/pubs/celiac/. Accessed December 9, 2009.
47. Rubio-Tapia A, Kyle RA, Kaplan EL, et al. Increased prevalence and mortality in undiagnosed celiac disease. Gastroenterology. 2009 Jul;137(1):88-93.
48. Lind L, Hanni A, Lithell H, et al. Vitamin D is related to blood pressure and other cardiovascular risk factors in middle-aged men. Am J Hypertens. 1995 Sep;8(9):894–901.
49. Forman JP, Curhan GC, Taylor EN. Plasma 25-hydroxyvitamin D levels and risk of incident hypertension among young women. Hypertension. 2008 Nov;52(5):828-32.
50. Pfeifer M, Begerow B, Minne HW, et al. Effects of a short-term vitamin D3 and calcium supplementation on blood pressure and parathyroid hormone levels in elderly women. J Clin Endcrinol Metab. 2001;86:1633–37.
51. Witham MD, Nadir MA, Struthers AD. Effect of vitamin D on blood pressure: a systematic review and meta-analysis. J Hypertens. 2009 Oct;27(10):1948-54.
52. Giovannucci E. Vitamin D and cardiovascular disease. Curr Atheroscler Rep. 2009 Nov;11(6):456-61.
53. Rosenfeldt FL, Haas SJ, Krum H, et al. Coenzyme Q10 in the treatment of hypertension: a meta-analysis of the clinical trials. J Hum Hypertens. 2007 Apr;21(4):297-306.
54. Devereux RB, Wachtell K, Gerdts E, et al. Prognostic significance of left ventricular mass change during treatment of hypertension. JAMA. 2004;292:2350-56.
55. Langsjoen PH, Folkers. Isolated diastolic dysfunction of the myocardium and its response to CoQ10 treatment. Clin Investig. 1993;71:S140-44.
56. Langsjoen P, Willis R, Folkers K. Treatment of essential hypertension with coenzyme Q10. Mol Aspects Med. 1994;15:S265-72.
57. Zibadi S, Rohdewald PJ, Park D, Watson RR. Reduction of cardiovascular risk factors in subjects with type 2 diabetes by pycnogenol supplementation. Nutr Res. 2008 May;28(5):315-20.
58. Liu X, Wei J, Tan F, Zhou S, Würthwein G, Rohdewald P. Pycnogenol, French maritime pine bark extract, improves endothelial function of hypertensive patients. Life Sci. 2004 Jan 2;74(7):855-62.
59. Rohdewald P. A review of the French maritime pine bark extract (pycnogenol), a herbal medication with a diverse clinical pharmacology. Int J Clin Pharmacol Ther. 2002 Apr;40(4):158-68.
60. Erlund I Koli R, Alfthan G, et al. Favorable effects of berry consumption on platelet function, blood pressure, and HDL cholesterol. Am J Clin Nutr. 2008;87:323-31.
61. Aviram M, Rosenblat M, Gaitini D, et al. Pomegranate juice consumption for 3 years by patients with carotid artery stenosis reduces common carotid intima-media thickness, blood pressure and LDL oxidation. Clin Nutr. 2004 Jun;23(3):423-33.
62. Ojeda D, Jiménez-Ferrer E, Zamilpa A, et al. Inhibition of angiotensin converting enzyme (ACE) activity by the anthocyanins delphinidin- and cyanidin-3-O-sambubiosides from Hibiscus sabdariffa. J Ethnopharmacol. 2009 Oct 4.
63. Xu JW, Ikeda K, Yamori Y. Upregulation of endothelial nitric oxide synthase by cyanidin-3-glucoside, a typical anthocyanin pigment. Hypertension. 2004 Aug;44(2):217-22.
64. Guerrera MP, Volpe SL, Mao JJ. Therapeutic uses of magnesium.Am Fam Physician. 2009 Jul 15;80(2):157-62.
65. Pham PC, Pham PM, Pham PT, et al. The link between lower serum magnesium and kidney function in patients with diabetes mellitus Type 2 deserves a closer look. Clin Nephrol. 2009 Apr;71(4):375-9.
66. Kawano Y, Matsuoka H, Takishita S, Omae T. Effects of magnesium supplementation in hypertensive patients: assessment by office, home, and ambulatory blood pressures. Hypertension. 1998 Aug;32(2):260-5.
67. Rayssiguier Y, Gueux E, Nowacki W et al. High fructose consumption combined with low dietary magnesium intake may increase the incidence of the metabolic syndrome by inducing inflammation. Magnes Res. 2006 Dec;19(4):237-43.
68. Hatzistavri LS, Sarafidis PA, Georgianos PI, et al. Oral magnesium supplementation reduces ambulatory blood pressure in patients with mild hypertension. Am J Hypertens. 2009 Oct;22(10):1070-5.
69. Baker WL, Kluger J, White CM, et al. Effect of magnesium L-lactate on blood pressure in patients with an implantable cardioverter defibrillator. Ann Pharmacother. 2009 Apr;43(4):569-76.
70. Guerrero-Romero F, Rodríguez-Morán M. The effect of lowering blood pressure by magnesium supplementation in diabetic hypertensive adults with low serum magnesium levels: a randomized, double-blind, placebo-controlled clinical trial. J Hum Hypertens. 2009 Apr;23(4):245-51.
71. Geleijnse JM, Giltay EJ, Grobbee DE, et al. Blood pressure response to fish oil supplementation: metaregression analysis of randomized trials. J Hypertens. 2002 Aug;20(8):1493-9.
72. Cicero AF, Ertek S, Borghi C. Omega-3 polyunsaturated fatty acids: their potential role in blood pressure prevention and management. Curr Vasc Pharmacol. 2009 Jul;7(3):330-7.
73. da Luz PL, Coimbra SR. Wine, alcohol and atherosclerosis: clinical evidences and mechanisms. Braz J Med Biol Res. 2004 Sep;37(9):1275-95.
74. Guarente L. Sirtuins in aging and disease. Cold Spring Harb Symp Quant Biol. 2007;72:483-8.
75. Inanaga K, Ichiki T, Matsuura H et al. Resveratrol attenuates angiotensin II-induced interleukin-6 expression and perivascular fibrosis. Hypertens Res. 2009 Jun;32(6):466-71.
76. Labinskyy N, Csiszar A, Veress G, et al. Vascular dysfunction in aging: potential effects of resveratrol, an anti-inflammatory phytoestrogen. Curr Med Chem. 2006;13(9):989-96.
77. Takahashi S, Uchiyama T, Toda K. Differential effect of resveratrol on nitric oxide production in endothelial f-2 cells. Biol Pharm Bull. 2009 Nov;32(11):1840-3.
78. Ruggenenti P, Cattaneo D, Loriga G, et al. Ameliorating hypertension and insulin resistance in subjects at increased cardiovascular risk: effects of acetyl-L-carnitine therapy. Hypertension. 2009 Sep;54(3):567-74.
79. Brotman DJ, Davidson MB, Boumitri M, Vidt DG. Impaired diurnal blood pressure variation and all-cause mortality. Am J Hypertens. 2008 Jan;21(1):92-7.
80. Scheer FA, Van Montfrans GA, van Someren EJ, et al. Daily nighttime melatonin reduces blood pressure in male patients with essential hypertension. Hypertension. 2004 Feb;43(2):192-7.
81. Grossman E, Laudon M, Yalcin R, et al. Melatonin reduces night blood pressure in patients with nocturnal hypertension. Am J Med. 2006 Oct;119(10):898-902.
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