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Dietary Supplements Under Attack
Life Extension Magazine (Life Extension Foundation) ^ | April 2009 | By William Faloon

Posted on 04/05/2009 9:16:13 AM PDT by aMorePerfectUnion

Near the end of 2008, the media ran headline news stories claiming that vitamins C, D, and E do not prevent heart attack, stroke, or breast cancer. Within five days, we posted a rebuttal on the home page of our website.

When these biased stories are launched, the media never gives us prior notice to prepare a response. That means the public only hears conventional medicine’s distorted side of the story.

What follows is a slightly modified version of how we responded to these unfounded attacks:

In the early 1990s, several large population studies showed significant reductions in cardiovascular disease in those who consumed vitamin C or vitamin E.1-6

The most widely reported study emanated from UCLA, where it was announced that men who took 800 mg a day of vitamin C lived six years longer than those who consumed the recommended daily allowance of 60 mg a day. The study, which evaluated 11,348 participants over a 10-year period of time, showed that higher vitamin C intake reduced cardiovascular disease mortality by 42%.7

These kinds of findings did not go unnoticed by the federal government, who subsequently invested hundreds of millions of dollars in an attempt to ascertain if relatively modest vitamin doses could prevent common age-related diseases.

In a recent study used by the media to attack dietary supplements, four groups of male doctors were given various combinations of vitamin C and/or vitamin E or placebo. After eight years, there was no reported difference in heart attack or stroke incidence among the groups.8 This led the media to state that consumers should not buy these supplements.

As you will read, there were so many flaws in this study that the findings are rendered meaningless. Regrettably, consumers who trust their lives to the mainstream media may fall victim to this latest charade to discredit validated methods to reduce cardiovascular disease risk.

Do You Take Your Vitamins Every Other Day?

In the study involving four groups of male doctors, subjects in the vitamin E groups were told to take one 400 IU capsule of synthetic alpha tocopherol every other day.8 This design flaw raises several issues that are rather obvious to serious supplement takers.

Do You Take Your Vitamins Every Other Day?

First of all, we don’t take our vitamins every other day. Free radicals are constantly being generated in our bodies, and supplement users today seek to take their antioxidants with most meals, as oxidative damage is generally the greatest after eating.9,10

It is ludicrous to think that these study subjects would reduce their vascular risk by taking a modest dose, every other day, of a form of vitamin E with inferior antioxidant capacity.

If one were to rely only on synthetic alpha tocopherol, the minimum daily dose needed has been shown to exceed 800 IU,11,12 far greater than the 400 IU ingested every other day by the subjects in this poorly designed study.

Serious supplement users normally take 400 IU every day of natural vitamin E along with a plethora of complementary nutrients. We would not expect 400 IU of synthetic vitamin E taken every other day to produce much of an effect. Yet that is the dose given to these study subjects with the expectation that this would produce a reduction in cardiovascular disease. This is not the only flaw of this study.

Natural Versus Synthetic Vitamin E

There was a longstanding debate as to whether natural or synthetic vitamin E is better. For most vitamins, there is no difference between natural and synthetic. In fact, for most vitamins, the only forms available are synthetic. With vitamin E, however, the natural form has proven to be far superior.4,13-16

Natural vitamin E is distributed through the body much better than the synthetic form.12,17-21 The reason is that specific carrier proteins in the liver selectively bind to natural vitamin E and transport it through the blood to our cells. These carrier proteins only recognize a portion of synthetic vitamin E and ignore the remainder.22-25

Japanese researchers gave natural or synthetic vitamin E to young women to measure how much vitamin E actually made it into their blood. It took only 100 mg (149 IU) of natural vitamin E to produce blood levels that required 300 mg (448 IU) of synthetic vitamin E to achieve.12

How to Check Vitamin E Labels

When checking vitamin labels, natural vitamin E is usually stated as the “d” form or RRR- [for example d-alpha tocopheryl acetate or RRR-alpha-tocopheryl acetate, d-alpha tocopherol, and d-alpha tocopheryl succinate]. Synthetic vitamin E will have an “l” after the “d” or all-rac- [for example, dl-alpha tocopheryl acetate or all-rac-alpha-tocopheryl acetate, dl-alpha tocopheryl succinate, and dl-alpha tocopherol]. Remember – “dl” or “all rac-” signifies synthetic vitamin E, whereas “d” or “RRR-” signifies natural vitamin E. If you are getting 400 IU of natural d-alpha tocopherol (d-alpha tocopheryl succinate or acetate), it is equal to about 800 IU of synthetic dl-tocopherol (dl-alpha tocopheryl succinate or acetate).

Most studies show that synthetic vitamin E is only half as active in the body as the natural form.17 As it relates to the flawed study claiming that vitamin E does not prevent heart attack, the 400 IU of synthetic alpha tocopherol given every other day equates to only 100 IU a day of the natural form.

We would not expect 100 IU of natural vitamin E a day by itself to reduce vascular disease risk. As you will continue to read, however, there are many other flaws in this study that render its conclusions useless.

Vitamin C Potencies Too Low

If all you are going to take to protect against free radical damage is vitamin E and/or vitamin C, then you will need far greater potencies than were given to the study subjects in this flawed study.

Vitamin C Potencies Too Low

Published studies that document vascular benefits in response to vitamin C typically use doses of 1,000-6,000 mg each day.26-31 The authors of the flawed study alluded8 to this when they stated:

“In a pooled analysis of nine cohorts, vitamin C supplement use exceeding 700 mg/day was significantly associated with a 25% reduction in coronary heart disease risk.”8,32

Since the doctors who designed this flawed study knew that vitamin C intakes exceeding 700 mg a day significantly reduce heart attack rates,32 we cannot figure out why they limited their subject’s daily dose to only 500 mg.8

Two-time Nobel Prize laureate Linus Pauling and his associates advocated daily doses of vitamin C ranging from 10,000 to 20,000 mg to protect against heart attack. Linus Pauling’s theory was that atherosclerosis is primarily caused by insufficient vitamin C intake.33 Dr. Pauling compared the high amount of vitamin C naturally synthesized in the bodies of animals that don’t typically die of heart attacks.34 A 150-pound goat, for example will maintain an ascorbate blood concentration equivalent to ingesting 13,000 mg of vitamin C.34

Unlike most animals, humans lack an internal enzyme needed to manufacture vitamin C in their body. If humans don’t obtain enough vitamin C from external sources, they die acutely from scurvy, or according to Linus Pauling…slowly suffer atherosclerotic occlusion. Dr. Pauling crusaded to educate humans about the need to take mega-doses of vitamin C.

Dr. Pauling and his associates published papers stating that when vitamin C levels are insufficient, the body uses cholesterol to repair the inner lining of arteries. Dr. Pauling believed that cholesterol’s involvement in atherosclerosis was a direct result of insufficient vitamin C.34-36

Life Extension has long recommended that its members take at least 2,000 mg a day of vitamin C, along with potent plant extracts to enhance the biological benefits of ascorbate inside the body. The 500 mg daily dose of vitamin C given to the subjects of this flawed study8 was clearly inadequate. This did not stop the headline-hungry media and many conventional doctors from recommending that aging humans avoid these supplements altogether.

Alpha Tocopherol Users Need CoQ10

A number of studies document the ability of ubiquinol CoQ10 to protect against LDL oxidation better than alpha tocopherol (and other lipid-soluble antioxidants).79-83

Some of these studies show that alpha tocopherol vitamin E can turn into an LDL pro-oxidant unless ubiquinol is also present.84,85 These studies help explain the inability of the alpha form of vitamin E by itself to significantly reduce heart attack rates in certain populations.

The good news is that most members have been taking CoQ10 supplements since around 1983 (when Life Extension introduced it to the American public) and have thus protected their alpha tocopherol from converting into a pro-oxidant.

The subjects given synthetic alpha tocopherol in this flawed study were not given CoQ10 supplements, which further explains why there were no reductions in heart attack and stroke risk.

As we noted already, the dose of vitamin E used in this study was also too low to expect a reduction in vascular disease events. While alpha tocopherol vitamin E is a classic antioxidant, its free radical-quenching efficacy pales in comparison to polyphenol extracts37 from green tea, pomegranate, grape seed, and blueberry.

Based on the superior anti-oxidant properties of plant extracts such as pomegranate, health-conscious people today are able to obtain greater protection against free radicals and enhance the efficacy of the vitamin C without necessarily having to take the mega-doses recommended by Linus Pauling. On the flip side, to attack the value of vitamin C based on a group of doctors who took only 500 mg a day does not make sense, since this amount does not correspond to the doses that scientific studies show are needed to prevent heart attack.

Alpha Tocopherol Displaces Gamma Tocopherol

An increasing number of scientists are questioning the wisdom of administering alpha tocopherol vitamin E by itself.38-42 The reason is that alpha tocopherol displaces critically important gamma tocopherol in the body.43 The authors of the flawed study admitted that the failure to include gamma tocopherol may have been a reason that no effect was seen in the alpha tocopherol groups.8 Here is a quote directly from the flawed study:

“Moreover, PHS II and other prevention trials have used alpha-tocopherol, whereas the gamma-tocopherol isomer also may have a role in cardiovascular disease prevention because it has greater efficacy than alpha-tocopherol to inhibit lipid peroxidation and it may be suppressed in the presence of alpha-tocopherol.”8

The above admission understates the critical importance that gamma tocopherol plays in maintaining arterial health. While alpha tocopherol helps protect against lipid peroxidation, gamma tocopherol is required to neutralize the dangerous peroxynitrite free radical.44

Peroxynitrite damages arteries because:

1. Peroxynitrite promotes the degradation of alpha tocopherol, thereby depleting the body of the vitamin E needed to protect the lipid (fat) part of LDL against oxidation.45 LDL is composed of both lipid and protein parts (moieties), and oxidation associated with both moieties has been implicated in atherosclerosis.46,47 In a fascinating paradox, when alpha tocopherol is given without gamma tocopherol, the result is that alpha tocopherol itself can be neutralized in the body by the peroxynitrite free radical. This in turn promotes oxidation of the lipid moiety of LDL, a major step on the path towards atherosclerosis.

2. Peroxynitrite promotes LDL protein oxidation.48-51 While alpha tocopherol inhibits LDL lipid peroxidation, gamma tocopherol is needed to protect against oxidation of the protein moiety of LDL.42,52,53

In the absence of gamma tocopherol, which can occur when alpha tocopherol is given without gamma tocopherol, both LDL lipid and protein oxidation is increased, which reveals the egregious mistake of trying to prevent vascular disease by administering only alpha tocopherol. Health-conscious individuals should be assured that other nutrients such as lipoic acid and polyphenol plant extracts also block protein and lipid LDL oxidation.9,54-62

Some studies suggest that only gamma tocopherol prevents heart attacks.6 As it relates to atherosclerosis, gamma tocopherol blood concentrations have been reported to be significantly lower in coronary heart disease patients than in healthy control subjects. While alpha and gamma tocopherols each perform life-sustaining functions, only gamma tocopherol increases endothelial nitric oxide protein expression.52,53,63 As I will describe next, a deficit of nitric oxide in the endothelium is a primary cause of arterial disease.

Vitamin E Basics

Alpha tocopherol and gamma tocopherol are the two major forms of vitamin E in human plasma. The dietary intake of gamma toco-pherol is generally two- to four-fold higher than that of alpha tocopherol. Alpha tocopherol plasma levels, however, are about four-fold higher than those of gamma tocopherol.64 One reason is that there is a preferential cellular uptake of gamma tocopherol over alpha tocopherol, meaning that more gamma tocopherol is removed from the blood and assimilated into cells.65

Scientific studies consistently show that gamma tocopherol plays a significant role in modulating intracellular antioxidant defense mechanisms.39,42,66 Interestingly, the presence of gamma tocopherol dramatically increases the cellular accumulation of alpha tocopherol.67

 

A Hidden Cause of Heart Attack and Stroke

Even when all conventional risk factors are controlled, the progressive decline of nitric oxide in the arterial wall (the endothelium) too often leads to coronary heart attack and stroke.68-75

A Hidden Cause of Heart Attack and Stroke

Seven years ago, Life Extension researchers identified a critical compound (tetrahydrobiopterin) that is an essential cofactor for the enzyme that synthesizes nitric oxide in the endothelium.76 We spent several hundred thousand dollars trying to develop an affordable way to manufacture this compound as it offered tremendous promise for eradicating atherosclerosis.

We failed to find an affordable way to make tetrahydrobiopterin. The good news is that nutrients that suppress peroxynitrite (like gamma tocopherol and pomegranate) increase endothelial nitric oxide by blocking the oxidation of tetrahydrobiopterin.77,78

Indeed, clinical studies show that supplemental gamma tocopherol enhances platelet endothelial nitric oxide synthase activity.52,53 Furthermore, a diet high in gamma tocopherol-rich walnuts improves endothelium-dependent vasodilation in those with high cholesterol.63

By administering only alpha tocopherol as was done in the flawed study, one would expect gamma tocopherol to be suppressed, peroxynitrite levels to increase, and precious tetrahydrobiopterin to be oxidized, thus depriving the endothelium of the nitric oxide it needs to protect against heart attack and stroke. Is it any wonder that this study failed to show vascular disease reduction in those given only alpha (but not gamma) tocopherol?

Failing to Account For All Vascular Risk Factors

Numerous independent risk factors are associated with the development of atherosclerosis and subsequent heart attack and stroke risk. A major flaw in this study was expecting low-dose vitamin C and/or E to somehow overcome all of these underlying causes of artery disease.

We know it is impossible for vitamins C and E to overcome these many risk factors, but this did not stop the media from recommending that Americans discard their supplements.

The following represents a succinct list of documented vascular disease risk factors:

  1. Low testosterone (in men)
  2. Excess fibrinogen
  3. Low HDL
  4. Excess LDL and total cholesterol
  5. Excess glucose
  6. Excess C-reactive protein
  7. Excess homocysteine
  8. Hypertension
  9. Low blood EPA/DHA
  10. Excess triglycerides
  11. Excess insulin
  12. Excess estrogen (in men)
  13. Oxidized LDL
  14. Excess platelet activity
  15. Nitric oxide deficit (endothelial dysfunction)
  16. Insufficient vitamin D
  17. Insufficient vitamin K2

The basis for doing this study, as outlined by the study’s authors, was to use vitamins C and/or E to:

  1. Trap organic free radicals… deactivate excited oxygen molecules… inhibit LDL oxidation
  2. Modify vascular reactivity… prevent tissue damage
  3. Modify platelet activity and thus reduce thrombotic potential.

As one can clearly see on the previous page, there are 17 documented cardiovascular risk factors. Yet only three of these risk factors are what formed the basis for conducting this low-dose vitamin C and/or E clinical trial. The three most important risk factors the authors of the flawed study expected to favorably influence with vitamins C and E were:

  1. LDL oxidation
  2. Platelet activity and thrombotic potential
  3. Vascular reactivity (another term for endothelial dysfunction).
Failing to Account For All Vascular Risk Factors

For every one mechanism the study’s authors proposed might enable low-dose vitamin C and/or synthetic vitamin E to work, there are five additional risk factors that would not be corrected. For instance, vitamins C and E in these low doses are not going to reduce C-reactive protein,86 homocysteine, fibrinogen, or glucose.87 Vitamins C and E in any dose are not going to increase testosterone, decrease estrogen, or provide cardioprotective EPA/DHA and vitamin D.

On the contrary, as we have already shown, by giving only alpha but not gamma tocopherol, one might expect increased LDL oxidation and impaired endothelial function. That’s because alpha tocopherol displaces gamma tocopherol in the body. Gamma tocopherol suppresses the peroxynitrite radical that oxidizes both LDL protein and the tetrahydrobiopterin that is needed to produce endothelial nitric oxide.

As far as platelet activity and thrombotic potential (abnormal clotting inside a blood vessel) are concerned, gamma tocopherol is significantly more potent than alpha tocopherol in inhibiting platelet aggregation that can lead to a heart attack or stroke.52,53 By displacing gamma tocopherol, the alpha tocopherol used alone in this study may have increased abnormal platelet aggregation risk.

From everything we know today, this study was designed to fail. Not only did it not correct for the major causes of vascular disease, but it may have exacerbated some of the more dangerous ones.

None of What I Wrote So Far May Really Matter

You have just learned why low-dose vitamin C and/or E supplementation would not be expected to reduce heart attack and stroke risk.

I have saved the biggest shocker for last. It turns out that a significant number of the study subjects (who were all medical doctors) who were supposed to take the vitamin C and/or E supplements did not take their pills. Yet when the calculations for heart attack or stroke incidence were made, those who took as little as 66% of their low-dose vitamin C and/or E supplements were counted as having taken the entire dose.

At the end of the study, 28% of the study subjects admitted they had not even taken 66% of their low-dose vitamin C and/or E supplements.

Even more troubling is the method used to track who was really taking their supplements. Participants were asked to remember and track supplement usage for over eight years’ time without any verification of actual pill counts, compliance by plasma antioxidant analysis, or in vivo surrogate markers of oxidative stress. Relying upon participants’ memory and recollection over a lengthy time period of many years is a rather pathetic way of ensuring adherence, and renders the authors’ so-called “sensitivity analysis” meaningless.

The lack of adherence, i.e., the fact that a significant percentage of the study participants were not even taking their vitamins, may be the most significant flaw to this study. No one in the mainstream media bothered to report this, or any of the other flaws that jumped out at us.

Instead, the media’s message was don’t waste your money on vitamin C or E pills. Many supplement users who are taking the right form and dose of their vitamin C and E nutrients may believe the media’s biased reporting.

Shocking Deficiencies of Vitamin E

The media used this horrific-ally flawed study as a basis to steer Americans away from vitamin C and E supplements. It’s as if all of the previous positive published studies disappeared overnight.

What was omitted is the fact that 92% of American men and 98% of American women do not consume the recommended dietary allowance of vitamin E in their diet. The federal government says Americans need 15 milligrams per day of vitamin E, yet even this minute amount is not found in the diets of the vast majority of people.88

This means that most Americans require a vitamin E supplement to avoid a chronic deficiency, but this important fact was conveniently left out of the news stories.

Conventional medicine says that severe vitamin E deficiency results mainly in neuro-logical symptoms such as impaired balance and coordination and muscle weakness. These neurological symptoms do not develop for 10-20 years, as it takes time for free radicals to inflict nerve damage in the absence of sufficient vitamin E. The reality is that chronic vitamin E deficiency adversely impacts virtually every cell of the body.89-94

Does Drug Money Influence How Medical Journals Report on Dietary Supplements?

A group of statistical researchers investigated the relationship between pharmaceutical advertising and articles regarding dietary supplements in medical journals.99 The analysis revealed that:

  1. Journals with the most pharmaceutical ads published significantly fewer major articles about dietary supplements per issue than journals with the fewest pharmaceutical ads (P < 0.001).
  2. The percentage of major articles concluding that dietary supplements were unsafe was 4% in journals with the fewest pharmaceutical ads and 67% among those with the most pharmaceutical ads (P < 0.005).
  3. The percentage of articles concluding that dietary supplements were ineffective was almost twice as high (50%) among journals with more pharmaceutical ads than among those with fewer pharmaceutical ads (27%).

The researchers concluded that increased pharmaceutical advertising is associated with the publication of fewer articles about dietary supplements and more articles with conclusions that dietary supplements are unsafe.99

A major reason why many conventional doctors are biased against dietary supplements is that the journals they read seldom publish the favorable studies. Dietary supplements compete directly against prescription drugs in many disease categories. When dietary supplements are properly used to prevent disease, demand for expensive pharmaceutical agents is diminished. It is thus in the financial interest of pharmaceutical companies to encourage negative studies to be published in influential medical journals.

It seems more than a coincidence that mainstream medical journals publish negative editorials against dietary supplements at times of the year that garner the most media coverage. Life Extension has long argued that the billions of advertising dollars spent by pharmaceutical companies influences media bias against dietary supplements. This latest study reveals that drug money may also be corrupting medical journals that have a significant impact on professional and public opinion.

A Media Coup for Pharmaceutical Companies

The optimal moment of the year to get your message to the masses is the second week of November. This is a time in between holidays, when winter is setting in, and few people are on vacation. The television networks consider this their most important “sweeps week” as it provides the most accurate measurement of their ratings.

Media Also Attacks Vitamin D

The timing of the release of this horrendously flawed vitamin C and E study could not have been more perfect for pharmaceutical interests. It came out less than one week after the November elections, when the media was primed to sensationalize any story that would attract viewers for their all important “sweeps week.”

On the very same day the media launched its attack on vitamins C and E, the same news sources reported that very high doses of the statin drug Crestor® reduced heart attack rates by 54% in healthy people who had high C-reactive protein levels.95 Just think, uneducated consumers read on the same day that vitamins C and E are worthless and an expensive statin drug performs miracles.

Financial analysts predict a windfall for the makers of Crestor® based on this widely distributed report. In retrospect, conducting a study only on people with high C-reactive protein (but not particularly high LDL) was a brilliant marketing strategy. It had a high probability of a successful outcome, and if the study failed, Crestor® was never approved to lower C-reactive protein or be used in this population group, so the pharmaceutical company had nothing to lose.

We at Life Extension have long warned about the vascular dangers of elevated C-reactive protein and even recommended statin drugs if natural approaches fail to reduce C-reactive protein. We don’t believe most people have to purchase expensive brand name drugs like Crestor®, as generic simvastatin (name brand Zocor®) or pravastatin (name brand Pravachol®) can provide similar benefit at a fraction of the price.

Media Also Attacks Vitamin D

Not content to bash only vitamins C and E, the media the very next day in November 2008 ran a headline story stating that “Supplements don’t reduce breast cancer risk.” This story was based on a study of women who received only 400 IU a day of supplemental vitamin D.96

Don’t Be a Victim of This Flawed Propaganda

As has been reported for years in this and other health publications, 400 IU a day of vitamin D is clearly inadequate.97 To reduce breast cancer risk by around 50%, a daily dose of 1,000 IU and higher is required. The major flaw in this study is that participants in the active and placebo group were allowed to take vitamin D outside the study, which rendered the findings meaningless even if the proper dose had been given.

The fact that the media made this study headline news is regrettable because only about 20% of the study population achieved a 25-hydroxyvitamin D blood result at the minimum level required to prevent breast cancer (approximately 30 ng/mL or higher). In other words, most participants in the active or placebo group failed to achieve even the minimal blood concentrations of vitamin D that other studies document are needed to protect against breast cancer.98 So all this study did was help confirm what vitamin D experts have been saying for over five years now, i.e., a minimum of 800 IU to 1,000 IU of vitamin D a day is required… not the 400 IU used in this study.

Don’t Be a Victim of This Flawed Propaganda

It 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.

As a member of the Life Extension Foundation, you gain access to scientific information that is interpreted in the context of what health-conscious people are really doing to protect themselves against age-related diseases. You also learn how this information is distorted by the government, drug companies, and the media to discourage the public from following healthier lifestyles.

References

1. Gey KF, Puska P, Jordan P, Moser UK. Inverse correlation between plasma vitamin E and mortality from ischemic heart disease in cross-cultural epidemiology. Am J Clin Nutr. 1991 Jan;53(1 Suppl):326S-34S.

2. Gey KF, Moser UK, Jordan P, et al. Increased risk of cardiovascular disease at suboptimal plasma concentrations of essential antioxidants: an epidemiological update with special attention to carotene and vitamin C. Am J Clin Nutr. 1993 May;57(5 Suppl):787S-97S.

3. Knekt P, Reunanen A, Jarvinen R, et al. Antioxidant vitamin intake and coronary mortality in a longitudinal population study. Am J Epidemiol. 1994 Jun 15;139(12):1180-9.

4. Losonczy KG, Harris TB, Havlik RJ. Vitamin E and vitamin C supplement use and risk of all-cause and coronary heart disease mortality in older persons: the Established Populations for Epidemio-logic Studies of the Elderly. Am J Clin Nutr. 1996 Aug;64(2):190-6.

5. Nyyssonen K, Parviainen MT, Salonen R, Tuomilehto J, Salonen JT. Vitamin C deficiency and risk of myocardial infarction: prospective population study of men from eastern Finland. BMJ. 1997 Mar 1;314(7081):634-8.

6. Kushi LH, Folsom AR, Prineas RJ, et al. Dietary antioxidant vitamins and death from coronary heart disease in postmenopausal women. N Engl J Med. 1996 May 2;334(18):1156-62.

7. Enstrom JE, Kanim LE, Klein MA. Vitamin C intake and mortality among a sample of the United States population. Epidemiology. 1992 May;3(3):194-202.

8. Sesso HD, Buring JE, Christen WG, et al. Vitamins E and C in the prevention of cardiovascular disease in men: the Physicians’ Health Study II randomized controlled trial. JAMA. 2008 Nov 12;300(18):2123-33.

9. Gorelik S, Lapidot T, Shaham I, et al. Lipid peroxidation and coupled vitamin oxidation in simulated and human gastric fluid inhibited by dietary polyphenols: health implications. J Agric Food Chem. 2005 May 4;53(9):3397-402.

10. Kanner J, Lapidot T. The stomach as a bioreactor: dietary lipid peroxidation in the gastric fluid and the effects of plant-derived antioxidants. Free Radic Biol Med. 2001 Dec 1;31(11):1388-95.

11. Devaraj S, Tang R, Adams-Huet B, et al. Effect of high-dose alpha-tocopherol supplementation on biomarkers of oxidative stress and inflammation and carotid atherosclerosis in patients with coronary artery disease. Am J Clin Nutr. 2007 Nov;86(5):1392-8.

12. Kiyose C, Muramatsu R, Kameyama Y, Ueda T, Igarashi O. Biodiscrimination of alpha-tocopherol stereoisomers in humans after oral administration. Am J Clin Nutr. 1997 Mar;65(3):785-9.

13. Wilburn EE, Mahan DC, Hill DA, Shipp TE, Yang H. An evaluation of natural (RRR-alpha-tocopheryl acetate) and synthetic (all-rac-alpha-tocopheryl acetate) vitamin E fortification in the diet or drinking water of weanling pigs. J Anim Sci. 2008 Mar;86(3):584-91.

14. Hayton SM, Kriss A, Wade A, Muller DP. The effects of different levels of all-rac- and RRR-alpha-tocopheryl acetate (vitamin E) on visual function in rats. Clin Neurophysiol. 2003 Nov;114(11):2124-31.

15. Hoppe PP, Krennrich G. Bioavailability and potency of natural-source and all-racemic alpha-tocopherol in the human: a dispute. Eur J Nutr. 2000 Oct;39(5):183-93.

16. Lodge JK. Vitamin E bioavailability in humans. J Plant Physiol. 2005 Jul;162(7):790-6.

17. Burton GW, Traber MG, Acuff RV, et al. Human plasma and tissue alpha-tocopherol concentrations in response to supplementation with deuterated natural and synthetic vitamin E. Am J Clin Nutr. 1998 Apr;67(4):669-84.

18. Traber MG. Utilization of vitamin E. Biofactors. 1999;10(2-3):115-20.

19. Blatt DH, Leonard SW, Traber MG. Vitamin E kinetics and the function of tocopherol regulatory proteins. Nutrition. 2001 Oct;17(10):799-805.

20. Rigotti A. Absorption, transport, and tissue delivery of vitamin E. Mol Aspects Med. 2007 Oct;28(5-6):423-36.

21. Blatt DH, Pryor WA, Mata JE, Rodriguez-Proteau R. Re-evaluation of the relative potency of synthetic and natural alpha-tocopherol: experimental and clinical observations. J Nutr Biochem. 2004 Jul;15(7):380-95.

22. Mustacich DJ, Bruno RS, Traber MG. Vitamin E. Vitam Horm. 2007;76:1-21.

23. Manor D, Morley S. The alpha-tocopherol transfer protein. Vitam Horm. 2007;76:45-65.

24. Morley S, Cecchini M, Zhang W, et al. Mechanisms of ligand transfer by the hepatic tocopherol transfer protein. J Biol Chem. 2008 Jun 27;283(26):17797-804.

25. Traber MG. Vitamin E regulatory mechanisms. Annu Rev Nutr. 2007;27:347-62.

26. Nappo F, De RN, Marfella R, et al. Impairment of endothelial functions by acute hyperhomocysteinemia and reversal by antioxidant vitamins. JAMA. 1999 Jun 9;281(22):2113-8.

27. Valkonen MM, Kuusi T. Vitamin C prevents the acute atherogenic effects of passive smoking. Free Radic Biol Med. 2000 Feb 1;28(3):428-36.

28. Jeserich M, Schindler T, Olschewski M, et al. Vitamin C improves endothelial function of epicardial coronary arteries in patients with hypercholesterolaemia or essential hypertension--assessed by cold pressor testing. Eur Heart J. 1999 Nov;20(22):1676-80.

29. Wilkinson IB, Megson IL, MacCallum H, et al. Oral vitamin C reduces arterial stiffness and platelet aggregation in humans. J Cardiovasc Pharmacol. 1999 Nov;34(5):690-3.

30. Jablonski KL, Seals DR, Eskurza I, Monahan KD, Donato AJ. High-dose ascorbic acid infusion abolishes chronic vasoconstriction and restores resting leg blood flow in healthy older men. J Appl Physiol. 2007 Nov;103(5):1715-21.

31. Hernandez-Guerra M, Garcia-Pagan JC, Turnes J, et al. Ascorbic acid improves the intrahepatic endothelial dysfunction of patients with cirrhosis and portal hypertension. Hepatology. 2006 Mar;43(3):485-91.

32. Knekt P, Ritz J, Pereira MA, et al. Antioxidant vitamins and coronary heart disease risk: a pooled analysis of 9 cohorts. Am J Clin Nutr. 2004 Dec;80(6):1508-20.

33. Rath M, Pauling L. Immunological evidence for the accumulation of lipoprotein(a) in the atherosclerotic lesion of the hypoascorbemic guinea pig. Proc Natl Acad Sci USA. 1990 Dec;87(23):9388-90.

34. Pauling L. Are recommended daily allowances for vitamin C adequate? Proc Natl Acad Sci USA. 1974 Nov;71(11):4442-6.

35. Krumdieck C, Butterworth CE, Jr. Ascorbate--cholesterol--lecithin interactions: factors of potential importance in the pathogenesis of atherosclerosis. Am J Clin Nutr. 1974 Aug;27(8):866-76.

36. Ginter E. Cholesterol: vitamin C controls its transformation to bile acids. Science. 1973 Feb 16;179(74):702-4.

37. Ferroni F, Maccaglia A, Pietraforte D, Turco L, Minetti M. Phenolic antioxidants and the protection of low density lipoprotein from peroxynitrite-mediated oxidations at physiologic CO2. J Agric Food Chem. 2004 May 19;52(10):2866-74

38. Helzlsouer KJ, Huang HY, Alberg AJ, et al. Association between alpha-tocopherol, gamma-tocopherol, selenium, and subsequent prostate cancer. J Natl Cancer Inst. 2000 Dec 20;92(24):2018-23.

39. Christen S, Woodall AA, Shigenaga MK, et al. gamma-tocopherol traps mutagenic electrophiles such as NO(X) and complements alpha-tocopherol: physiological implications. Proc Natl Acad Sci USA. 1997 Apr 1;94(7):3217-22.

40. Devaraj S, Leonard S, Traber MG, Jialal I. Gamma-tocopherol supplementation alone and in combination with alpha-tocopherol alters biomarkers of oxidative stress and inflammation in subjects with metabolic syndrome. Free Radic Biol Med. 2008 Mar 15;44(6):1203-8.

41. Reiter E, Jiang Q, Christen S. Anti-inflammatory properties of alpha- and gamma-tocopherol. Mol Aspects Med. 2007 Oct;28(5-6):668-91.

42. Jiang Q, Elson-Schwab I, Courtemanche C, Ames BN. gamma-tocopherol and its major metabolite, in contrast to alpha-tocopherol, inhibit cyclooxygenase activity in macrophages and epithelial cells. Proc Natl Acad Sci USA. 2000 Oct 10;97(21):11494-9.

43. Handelman GJ, Machlin LJ, Fitch K, Weiter JJ, Dratz EA. Oral alpha-tocopherol supplements decrease plasma gamma-tocopherol levels in humans. J Nutr. 1985 Jun;115(6):807-13.

44. Wolf G. Gamma-Tocopherol: an efficient protector of lipids against nitric oxide-initiated peroxidative damage. Nutr Rev. 1997 Oct;55(10):376-8.

45. Botti H, Batthyány C, Trostchansky A, Radi R, Freeman BA, Rubbo H. Peroxynitrite-mediated alpha-tocopherol oxidation in low-density lipoprotein: a mechanistic approach. Free Radic Biol Med. 2004 Jan 15;36(2):152-62.

46. Yla-Herttuala S, Palinski W, Rosenfeld ME, et al. Evidence for the presence of oxidatively modified low density lipoprotein in atherosclerotic lesions of rabbit and man. J Clin Invest. 1989 Oct;84(4):1086-95.

47. Steinberg D, Carew TE, Fielding C, et al. Lipoproteins and the pathogenesis of atherosclerosis. Circulation. 1989 Sep;80(3):719-23.

48. Torres-Rasgado E, Fouret G, Carbonneau MA, Leger CL. Peroxynitrite mild nitration of albumin and LDL-albumin complex naturally present in plasma and tyrosine nitration rate-albumin impairs LDL nitration. Free Radic Res. 2007 Mar;41(3):367-75.

49. Uno M, Kitazato KT, Suzue A, Itabe H, Hao L, Nagahiro S. Contribution of an imbalance between oxidant-antioxidant systems to plaque vulnerability in patients with carotid artery stenosis. J Neurosurg. 2005 Sep;103(3):518-25.

50. Botti H, Trostchansky A, Batthyány C, Rubbo H. Reactivity of peroxynitrite and nitric oxide with LDL. IUBMB Life. 2005 Jun;57(6):407-12.

51. Rubbo H, Batthyany C, Radi R. Nitric oxide-oxygen radicals interactions in atherosclerosis. Biol Res. 2000;33(2):167-75.

52. Li D, Saldeen T, Romeo F, Mehta JL. Relative Effects of alpha- and gamma-Tocopherol on Low-Density Lipoprotein Oxidation and Superoxide Dismutase and Nitric Oxide Synthase Activity and Protein Expression in Rats. J Cardiovasc Pharmacol Ther. 1999 Oct;4(4):219-26.

53. Saldeen T, Li D, Mehta JL. Differential effects of alpha- and gamma-tocopherol on low-density lipoprotein oxidation, superoxide activity, platelet aggregation and arterial thrombogenesis. J Am Coll Cardiol. 1999 Oct;34(4):1208-15.

54. Mikunis RI, Serkova VK, Shirkova TA. Lipid metabolism and oxidation-reduction properties of blood in patients with arteriosclerotic myocardiosclerosis during treatment with lipoic acid. Vrach Delo. 1976 Mar;(3):39-42.

55. Nickander KK, McPhee BR, Low PA, Tritschler H. Alpha-lipoic acid: antioxidant potency against lipid peroxidation of neural tissues in vitro and implications for diabetic neuropathy. Free Radic Biol Med. 1996;21(5):631-9.

56. Packer L, Tritschler HJ, Wessel K. Neuroprotection by the metabolic antioxidant alpha-lipoic acid. Free Radic Biol Med. 1997;22(1-2):359-78.

57. Arivazhagan P, Shila S, Kumaran S, Panneerselvam C. Effect of DL-alpha-lipoic acid on the status of lipid peroxidation and antioxidant enzymes in various brain regions of aged rats. Exp Gerontol. 2002 Jun;37(6):803-11.

58. Arivazhagan P, Thilakavathy T, Ramanathan K, Kumaran S, Panneerselvam C. Effect of DL-alpha-lipoic acid on the status of lipid peroxidation and protein oxidation in various brain regions of aged rats. J Nutr Biochem. 2002 Oct;13(10):619-24.

59. Ozgova S, Hermanek J, Gut I. Different antioxidant effects of polyphenols on lipid peroxidation and hydroxyl radicals in the NADPH-, Fe-ascorbate- and Fe-microsomal systems. Biochem Pharmacol. 2003 Oct 1;66(7):1127-37.

60. Thirunavukkarasu V, Anuradha CV. Influence of alpha-lipoic acid on lipid peroxidation and antioxidant defence system in blood of insulin-resistant rats. Diabetes Obes Metab. 2004 May;6(3):200-7.

61. Thirunavukkarasu V, Anitha Nandhini AT, Anuradha CV. Cardiac lipids and antioxidant status in high fructose rats and the effect of alpha-lipoic acid. Nutr Metab Cardiovasc Dis. 2004 Dec;14(6):351-7.

62. Singh I, Turner AH, Sinclair AJ, Li D, Hawley JA. Effects of gamma-tocopherol supplementation on thrombotic risk factors. Asia Pac J Clin Nutr. 2007;16(3):422-8.

63. Ros E, Nunez I, Perez-Heras A, et al. A walnut diet improves endothelial function in hypercholesterolemic subjects: a randomized crossover trial. Circulation. 2004 Apr 6;109(13):1609-14.

64. Dietrich M, Traber MG, Jacques PF, Cross CE, Hu Y, Block G. Does gamma-tocopherol play a role in the primary prevention of heart disease and cancer? A review. J Am Coll Nutr. 2006 Aug;25(4):292-9.

65. McLaughlin PJ, Weihrauch JL. Vitamin E content of foods. J Am Diet Assoc. 1979 Dec;75(6):647-65.

66. Tanaka Y, Wood LA, Cooney RV. Enhancement of intracellular gamma-tocopherol levels in cytokine-stimulated C3H 10T1/2 fibroblasts: relation to NO synthesis, isoprostane formation, and tocopherol oxidation. BMC Chem Biol. 2007;72.

67. Gao R, Stone WL, Huang T, Papas AM, Qui M. The uptake of tocopherols by RAW 264.7 macrophages. Nutr J. 2002 Oct 15;12.

68. Giannotti G, Landmesser U. Endothelial dysfunction as an early sign of atherosclerosis. Herz. 2007 Oct;32(7):568-72.

69. Pesic S, Radenkovic M, Grbovic L. Endothelial dysfunction: mechanisms of development and therapeutic options. Med Pregl. 2006 Jul-Aug;59(7-8):335-41.

70. Halcox JP, Schenke WH, Zalos G, et al. Prognostic value of coronary vascular endothelial dysfunction. Circulation. 2002 Aug 6;106(6):653-8.

71. Targonski PV, Bonetti PO, Pumper GM, et al. Coronary endothelial dysfunction is associated with an increased risk of cerebrovascular events. Circulation. 2003 Jun 10;107(22):2805-9.

72. von Mering GO, Arant CB, Wessel TR, et al. Abnormal coronary vasomotion as a prognostic indicator of cardiovascular events in women: results from the National Heart, Lung, and Blood Institute-Sponsored Women’s Ischemia Syndrome Evaluation (WISE). Circulation. 2004 Feb 17;109(6):722-5.

73. Heitzer T, Schlinzig T, Krohn K, Meinertz T, Munzel T. Endothelial dysfunction, oxidative stress, and risk of cardiovascular events in patients with coronary artery disease. Circulation. 2001 Nov 27;104(22):2673-8.

74. Chan SY, Mancini GB, Kuramoto L, et al. The prognostic importance of endothelial dysfunction and carotid atheroma burden in patients with coronary artery disease. J Am Coll Cardiol. 2003 Sep 17;42(6):1037-43.

75. Brevetti G, Silvestro A, Schiano V, Chiariello M. Endothelial dysfunction and cardiovascular risk prediction in peripheral arterial disease: additive value of flow-mediated dilation to ankle-brachial pressure index. Circulation. 2003 Oct 28;108(17):2093-8.

76. Ali ZA, Bursill CA, Douglas G, et al. CCR2-mediated antiinflammatory effects of endothelial tetrahydrobiopterin inhibit vascular injury-induced accelerated atherosclerosis. Circulation. 2008 Sep 30;118(14 Suppl):S71-7.

77. McCarty MF. Gamma-tocopherol may promote effective no synthase function by protecting tetrahydrobiopterin from peroxynitrite. Med Hypotheses. 2007;69(6):1367-70.

78. de Nigris F, Balestrieri ML, Williams-Ignarro S, et al. The influence of pomegranate fruit extract in comparison to regular pomegranate juice and seed oil on nitric oxide and arterial function in obese Zucker rats. Nitric Oxide. 2007 Aug;17(1):50-4.

79. Stocker R, Bowry VW, Frei B. Ubiquinol-10 protects human low density lipoprotein more efficiently against lipid peroxidation than does alpha-tocopherol. Proc Natl Acad Sci USA. 1991 Mar 1;88(5):1646-50.

80. Frei B, Kim MC, Ames BN. Ubiquinol-10 is an effective lipid-soluble antioxidant at physiological concentrations. Proc Natl Acad Sci USA. 1990 Jun;87(12):4879-83.

81. Thomas SR, Neuzil J, Stocker R. Inhibition of LDL oxidation by ubiquinol-10. A protective mechanism for coenzyme Q in atherogenesis? Mol Aspects Med. 1997;18(Suppl):S85-103.

82. Mohr D, Bowry VW, Stocker R. Dietary supplementation with coenzyme Q10 results in increased levels of ubiquinol-10 within circulating lipoproteins and increased resistance of human low-density lipoprotein to the initiation of lipid peroxidation. Biochim Biophys Acta. 1992 Jun 26;1126(3):247-54.

83. Kontush A, Hubner C, Finckh B, Kohlschutter A, Beisiegel U. Antioxidative activity of ubiquinol-10 at physiologic concentrations in human low density lipoprotein. Biochim Biophys Acta. 1995 Sep 14;1258(2):177-87.

84. Bowry VW, Mohr D, Cleary J, Stocker R. Prevention of tocopherol-mediated peroxidation in ubiquinol-10-free human low density lipoprotein. J Biol Chem. 1995 Mar 17;270(11):5756-63.

85. Tribble DL, van den Berg JJ, Motchnik PA, et al. Oxidative susceptibility of low density lipoprotein subfractions is related to their ubiquinol-10 and alpha-tocopherol content. Proc Natl Acad Sci USA. 1994 Feb 1;91(3):1183-7.

86. Block G, Jensen CD, Dalvi TB, et al. Vitamin C treatment reduces elevated C-reactive protein. Free Radic Biol Med. 2009 Jan 1;46(1):70-7.

87. Afkhami-Ardekani M, Shojaoddiny-Ardekani A. Effect of vitamin C on blood glucose, serum lipids & serum insulin in type 2 diabetes patients. Indian J Med Res. 2007 Nov;126(5):471-4.

88. Maras JE, Bermudez OI, Qiao N, et al. Intake of alpha-tocopherol is limited among US adults. J Am Diet Assoc. 2004 Apr;104(4):567-75.

89. Puri V, Chaudhry N, Tatke M, Prakash V. Isolated vitamin E deficiency with demyelinating neuropathy. Muscle Nerve. 2005 Aug;32(2):230-5.

90. Schuelke M, Finckh B, Sistermans EA, et al. Ataxia with vitamin E deficiency: biochemical effects of malcompliance with vitamin E therapy. Neurology. 2000 Nov 28;55(10):1584-6.

91. Tanyel MC, Mancano LD. Neurologic findings in vitamin E deficiency. Am Fam Physician. 1997 Jan;55(1):197-201.

92. Sokol RJ. Vitamin E deficiency and neurologic disease. Annu Rev Nutr. 1988;8:351-73.

93. Satya-Murti S, Howard L, Krohel G, Wolf B. The spectrum of neurologic disorder from vitamin E deficiency. Neurology. 1986 Jul;36(7):917-21.

94. Laplante P, Vanasse M, Michaud J, Geoffroy G, Brochu P. A progressive neurological syndrome associated with an isolated vitamin E deficiency. Can J Neurol Sci. 1984 Nov;11(4 Suppl):561-4.

95. Available at: http://www.medpagetoday.com/MeetingCoverage/AHA/11684. Accessed January 20, 2009.

96. Chlebowski RT, Johnson KC, Kooperberg C, et al. Calcium plus vitamin D supplementation and the risk of breast cancer. J Natl Cancer Inst. 2008 Nov 19;100(22):1581-91.

97. Garland CF, Garland FC, Gorham ED, et al. The role of vitamin D in cancer prevention. Am J Public Health. 2006 Feb;96(2):252-61.

98. Neuhouser ML, Sorensen B, Hollis BW, et al. Vitamin D insufficiency in a multiethnic cohort of breast cancer survivors. Am J Clin Nutr. 2008 Jul;88(1):133-9.

99. Kemper KJ, Hood KL. Does pharmaceutical advertising affect journal publication about dietary supplements? BMC Complement Altern Med. 2008;811.



TOPICS: Health/Medicine
KEYWORDS: health; supplements; vitamins
Lots of information that counterbalances the media reporting of supplements
1 posted on 04/05/2009 9:16:13 AM PDT by aMorePerfectUnion
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To: aMorePerfectUnion
I thought groups were looking into whether or not vitamins cause cancer...
2 posted on 04/05/2009 9:25:32 AM PDT by GOPJ (The Queen gave Obama a signed photograph. What did she give President Bush?)
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To: aMorePerfectUnion

The bottom line question of the day is:

How many of the overpriced packaged vitamins on the shelves today are from China?

http://www.alibaba.com/catalogs/160417/Vitamins_Amino_Acids_and_Coenzymes.html


3 posted on 04/05/2009 9:30:43 AM PDT by angkor
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To: aMorePerfectUnion; GOPJ

UN’s Codex Alimentarius is looming over us. Lots of info online. Here’s a short description written by Sue McIntosh, M.D, a retired pediatric oncologist.

Posted by mcintosh.sue on Feb 17 2009,

“The Codex Alimentarius is a CORPORATE list of ALL substances which will be legal to put in our mouths after it is implemented in the U.S. on 12/31/09.

” All vitamins, supplements, organic foods, clean water, raw milk, etc., will be ILLEGAL in the U.S. and in the North American Union (planned fusion of U.S. with Canada and Mexico) after the end of this calendar year.

“This is why the news media is trying to terrify Americans about food—the recent peanut butter-Salmonella thing, the spinach and tomato things last year, and more to come. “They” are laying the groundwork to implement radiation of ALL FOOD sold in the U.S.—”problem-reaction-solution.”

“This is why, all of a sudden, vitamins and minerals “do nothing” for you.

“This is the face of the New World Order (NWO), folks, and we need to do everything in our power to upset their plans and say a fierce, loud, NO! to the Codex Alimentarius. What you read or hear about it tries to sell it as a “food safety” measure. What they are really doing is trying to wipe out all natural food stores, organic food sources, all vitamins/minerals/supplements not currently made by the pharmaceutical industry so that the industry can take over the manufacture and sale of all these things. As usual, it’s all about profits for the rich.”

End of mcintosh quote. One thing she failed to mention is that Codex has been funded for decades by by Bayer, the German BigPharma mfg of aspirin and a whole lot more. If products in health food stores are outlawed, they can sell them as prescriptions. (Imagine Vitamin C for $100 for a month’s supply.)

In ‘85, I met a department head from Lilly in Germany. He was there buying up homeopathic formulas. So those little tabs I used to get for $4 that never failed to cure a cold will soon be $44, and probably require a prescription. Or just disappear, which I think happened because...they’ve disappeared.

Codex Alimentarius links at #1:

The UN/WTO Codex criminalizes vitamins, supplements and herbs: http://www.freerepublic.com/focus/f-news/1353912/posts

With Ibn al’0bama so cozy with the UN, I believe we are in grave danger of losing our rights to nutritional standards somewhat higher than those who live in Third World huts.

Just another way he can hurt us. Bring America to her knees by making Americans financially and physically weak. The genuflection he made to King Saud said it all.


4 posted on 04/05/2009 9:32:03 AM PDT by Veto! (Opinions freely dispensed as advice)
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To: GOPJ

This article sheds light on that...


5 posted on 04/05/2009 9:48:34 AM PDT by aMorePerfectUnion ("I, El Rushbo -- and I say this happily -- have hijacked Obama's honeymoon.")
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To: aMorePerfectUnion

thanks.


6 posted on 04/05/2009 10:07:24 AM PDT by ken21 (the only thing we have to fear is fdr deja vu.)
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To: aMorePerfectUnion

bttt


7 posted on 04/05/2009 10:16:58 AM PDT by aberaussie
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To: aMorePerfectUnion

I read where aspirin is as effective as statin drugs at reducing heart attacks, at a fraction of the cost. A handful of walnuts and a 20 minute nap everyday can reduce your risk of heart disease.A study where 21 ounces of green tea daily reduced risk factors for heart disease by 60%,in 8 weeks, the doctors doing the study admitted that there aren’t drugs powerful enough to do that.The list goes on.I’m convinced that food from God’s green earth can treat a lot of ailments.A lot of problems stem from over processed food.


8 posted on 04/05/2009 10:50:37 AM PDT by kickonly88
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To: aMorePerfectUnion

Why can’t people just get off their butts, exercise and eat right?

I NEVER take supplements and only take medication if a doctor tells me to and then the bare minimum if any.


9 posted on 04/05/2009 11:38:17 AM PDT by rfreedom4u (Diversity causes division and resentment.)
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To: rfreedom4u
I NEVER take supplements and only take medication if a doctor tells me to and then the bare minimum if any.

I agree. Most Vitamin C and vitamin B you take from a supplement is excreted in the urine. So if you want very expensive urine, take megadoses of Vit. C and B if it makes you feel better. Evolution programmed us to get our vitamins and other nutrients from food, not pills. Blueberries for example have some vitamin C but they've got other phyto-nutrients you can't get in a tablet.
10 posted on 04/05/2009 12:10:17 PM PDT by Signalman
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