(Redirected from Vitamin E)
Jump to navigation Jump to search

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [3]; Associate Editor(s)-in-Chief: Cafer Zorkun, M.D., Ph.D. [4]; Raviteja Guddeti, M.B.B.S. [5] Template:Search infobox

Template:Chembox new


Tocopherol, a class of chemical compounds of which many have vitamin E activity, describes a series of organic compounds consisting of various methylated phenols. Because the vitamin activity was first identified in 1936 from a dietary fertility factor in rats, it was given the name "tocopherol" from the Greek words “τοκος” [birth], and “φορειν”, [to bear or carry] meaning in sum "to carry a pregnancy," with the ending "-ol" signifying its status as a chemical alcohol.

Tocotrienols, which are related compounds, may also have vitamin E activity. All of these various derivatives with vitamin activity, may correctly be referred to as "vitamin E". Tocopherols and tocotrienols are fat-soluble antioxidants.

The compound α-tocopherol, a common form of tocopherol added to food products, is denoted by the E number "E307".


Natural vitamin E exists in eight different forms, four tocopherols and four tocotrienols. All feature a chromanol ring, with a hydroxyl group that can donate a hydrogen atom to reduce free radicals and a hydrophobic side chain which allows for penetration into biological membranes. Both the tocopherols and tocotrienols occur in alpha, beta, gamma and delta forms, determined by the number of methyl groups on the chromanol ring. Each form has slightly different biological activity.[1]

As a food additive, tocopherol is labeled with these E numbers: "E307" (α-tocopherol), "E308" (γ-tocopherol), and "E309" (δ-tocopherol). Vitamin E capsules are sometimes used as visible markers in magnetic resonance imaging.


Alpha-tocopherol is traditionally considered the most active biological antioxidant in humans. The measurement of "vitamin E" activity in international units (IU) was based on fertility enhancement by the prevention of spontaneous abortions in pregnant rats relative to alpha tocopherol. It increases naturally to about 150% of normal in the maternal circulation during human pregnancies.

1 IU of tocopherol is defined as ⅔ milligrams of RRR-alpha-tocopherol (formerly named d-alpha-tocopherol or sometimes ddd-alpha-tocopherol). 1 IU is also defined as 1 milligram of the 8-isomer mix all-rac-alpha-tocopheryl acetate (commercially now "called" dl-alpha-tocopheryl acetate, even though it is more precisely dl,dl,dl-alpha-tocopherol acetate). However, 1 IU of this racemic mixture is not now considered equivalent to 1 IU of natural (RRR) α-tocopherol, and the Institute of Medicine and the USDA now convert IU's of the racemic mixture to milligrams of equivalent RRR using 1 IU racemic mixture = 0.45 "milligrams α-tocopherol".[2]

The original dl,l,l semi-synthetic molecular mix, originally called dl-alpha-tocopherol acetate also, but actually more precisely known as 2-ambo-alpha-tocopherol, is no longer manufactured.

Pill Images

{{#ask: Page Name::Tocopherol |?Pill Name |?Drug Name |?Pill Ingred |?Pill Imprint |?Pill Dosage |?Pill Color |?Pill Shape |?Pill Size (mm) |?Pill Scoring |?NDC |?Drug Author |format=template |template=DrugPageImages |mainlabel=- |sort=Pill Name }} {{#subobject:

 |Page Name=Tocopherol
 |Pill Name=PRENATAL_PLUS_IRON_NDC_09045339.jpg
 |Pill Imprint=CIS28;G13
 |Pill Dosage=22 [iU]
 |Pill Color=Yellow|+sep=;
 |Pill Shape=Oval
 |Pill Size (mm)=18
 |Pill Scoring=1
 |Pill Image=
 |Drug Author=Major Pharmaceuticals



 |Page Name=Tocopherol
 |Pill Name=Se-Care_Chewable_NDC_139250104.jpg
 |Drug Name=Se-Care Chewable
 |Pill Imprint=TL014
 |Pill Dosage=3.5 [iU]
 |Pill Color=Grey|+sep=;
 |Pill Shape=Round
 |Pill Size (mm)=12
 |Pill Scoring=1
 |Pill Image=
 |Drug Author=Seton Pharmaceuticals



 |Page Name=Tocopherol
 |Pill Name=Zatean-CH_NDC_138110583.jpg
 |Drug Name=Zatean-CH
 |Pill Ingred=Calcium Citrate[Calcium Cation];Iron[Iron];Cholecalciferol[Cholecalciferol];Alpha-Tocopherol Acetate;DL-[Alpha-Tocopherol Acetate;DL-];Pyridoxine Hydrochloride[Pyridoxine];Folic Acid[Folic Acid];Docusate Sodium[Docusate];Doconexent[Doconexent]|+sep=;
 |Pill Imprint=T583
 |Pill Dosage=30 [iU]
 |Pill Color=Purple|+sep=;
 |Pill Shape=Oval
 |Pill Size (mm)=25
 |Pill Scoring=1
 |Pill Image=
 |Drug Author=TRIGEN Laboratories, Inc.



 |Page Name=Tocopherol
 |Pill Name=PRENATAL_PLUS_NDC_651620668.jpg
 |Pill Imprint=G12
 |Pill Dosage=22 mg
 |Pill Color=Yellow|+sep=;
 |Pill Shape=Oval
 |Pill Size (mm)=19
 |Pill Scoring=1
 |Pill Image=
 |Drug Author=Amneal Pharmaceuticals, LLC



 |Page Name=Tocopherol
 |Pill Name=PreNatal_Vitamins_Plus_NDC_643760816.jpg
 |Drug Name=PreNatal Vitamins Plus
 |Pill Imprint=BP;816
 |Pill Dosage=22 mg
 |Pill Color=White|+sep=;
 |Pill Shape=Oval
 |Pill Size (mm)=19
 |Pill Scoring=1
 |Pill Image=
 |Drug Author=Boca Pharmacal, Inc.


Other R, R, R Tocopherol

The other R, R, R tocopherol vitamins are slowly being recognized as research begins to elucidate their additional roles in the human body. Many naturopathic and orthomolecular medicine advocates suggest that vitamin E supplements contain at least 20% by weight of the other natural vitamin E isomers.


Tocotrienols, with four d- isomers, also belong to the vitamin E family. The four tocotrienols have structures corresponding to the four tocopherols, except with an unsaturated bond in each of the three isoprene units that form the hydrocarbon tail. Tocopherols have a saturated phytyl tail.


During feeding experiments with rats Herbert McLean Evans concluded in 1922 that besides vitamins B and C, an unknown vitamin existed.[3] Although every other nutrition was present, the rats were not fertile. This condition could be changed by additional feeding with wheat germ. It took several years until 1936 when the substance was isolated from wheat germ and the formula C29H50O2 was determined. Evans also found that the compound reacted like an alcohol and concluded that one of the oxygen atoms was part of an OH (hydroxyl) group. As noted in the introduction, the vitamin was given its name by Evans from Greek words meaning "to bear young" with the addition of the -ol as an alcohol.[4] The structure was determined shortly thereafter in 1938.[5]

Recommended Amounts

The U.S. Dietary Reference Intake (DRI) Recommended Daily Amount (RDA) for a 25-year old male for Vitamin E is 15 mg/day. The DRI for vitamin E is based on the alpha-tocopherol form because it is the most active form as originally tested. Results of two national surveys, the National Health and Nutrition Examination Survey (NHANES III 1988-91) and the Continuing Survey of Food Intakes of Individuals (1994 CSFII) indicated that the dietary intakes of most Americans do not provide the recommended amounts of vitamin E. However, a 2000 Institute of Medicine (IOM) report on vitamin E states that intake estimates of vitamin E may be low because energy and fat intake is often underreported in national surveys and because the kind and amount of fat added during cooking is often not known. The IOM states that most North American adults get enough vitamin E from their normal diets to meet current recommendations. However, they do caution individuals who consume low fat diets because vegetable oils are such a good dietary source of vitamin E. "Low-fat diets can substantially decrease vitamin E intakes if food choices are not carefully made to enhance alpha-tocopherol intakes". Vitamin E supplements are absorbed best when taken with meals.[6]

Because vitamin E can act as an anticoagulant and may increase the risk of bleeding problems, many agencies have set an upper tolerable intake level (UL) for vitamin E at 1,000 mg (1,500 IU) per day.[7]


In foods, the most abundant sources of vitamin E are vegetable oils such as palm oil, sunflower, corn, soybean, and olive oil. Nuts, sunflower seeds, seabuckthorn berries, kiwi fruit, and wheat germ are also good sources. Other sources of vitamin E are whole grains, fish, peanut butter, goats milk, and green leafy vegetables. Fortified breakfast cereals are also an important source of vitamin E in the United States. Although originally extracted from wheat germ oil, most natural vitamin E supplements are now derived from vegetable oils, usually soybean oil.

The content of Vitamin E for rich sources follows:[8]


There are three specific situations when a vitamin E deficiency is likely to occur. It is seen in persons who cannot absorb dietary fat, has been found in premature, very low birth weight infants (birth weights less than 1500 grams, or 3.5 pounds), and is seen in individuals with rare disorders of fat metabolism. A vitamin E deficiency is usually characterized by neurological problems due to poor nerve conduction.

Individuals who cannot absorb fat may require a vitamin E supplement because some dietary fat is needed for the absorption of vitamin E from the gastrointestinal tract. Anyone diagnosed with cystic fibrosis, individuals who have had part or all of their stomach removed, and individuals with malabsorptive problems such as Crohn's disease, liver disease or pancreatic insufficiency may not absorb fat and should discuss the need for supplemental vitamin E with their physician (3). People who cannot absorb fat often pass greasy stools or have chronic diarrhea and bloating.

Very low birth weight infants may be deficient in vitamin E. A neonatologist, a pediatrician specializing in the care of newborns, typically evaluates the nutritional needs of premature infants.

Abetalipoproteinemia is a rare inherited disorder of fat metabolism that results in poor absorption of dietary fat and vitamin E. The vitamin E deficiency associated with this disease causes problems such as poor transmission of nerve impulses, muscle weakness, and degeneration of the retina that can cause blindness. Individuals with abetalipoproteinemia may be prescribed special vitamin E supplements by a physician to treat this disorder. In addition, there is a rare genetic condition termed isolated vitamin E deficiency or ataxia with isolated with vitamin E deficiency, caused by mutations in the tocopherol transfer protein gene. These individuals have an extremely poor capacity to absorb vitamin E and develop neurological complications that are reversible by supplementation with high doses of vitamin E.

Also, in adults, erythrocyte membrane fragility results as the erythrocytes are oxidized.


Commercial vitamin E supplements can be classified into several distinct categories:

  • Fully synthetic vitamin E, "dl-alpha-tocopherol", the most inexpensive, most commonly sold supplement form usually as the acetate ester;
  • Semi-synthetic "natural source" vitamin E esters, the "natural source" forms used in tablets and multiple vitamins. These are highly fractionated d-alpha tocopherol or its esters, often made by synthetic methylation of gamma and beta d,d,d tocopherol vitamers extracted from plant oils.
  • Less fractionated "natural mixed tocopherols" and high d-gamma-tocopherol fraction supplements

Synthetic All-racemic

Synthetic vitamin E derived from petroleum products is manufactured as all-racemic alpha tocopheryl acetate with three chiral centers. This mixture has only one alpha tocopherol molecule (moiety) in 8 molecules as actual R, R,R-alpha tocopherol.

The 8-isomer "all-rac" vitamin E is always marked on labels simply as "dl-tocopherol" or "dl-tocopheryl acetate", even though it is (if fully written out) actually dl,dl,dl-tocopherol. The present largest manufacturers of this type are DSM and BASF.

(An earlier semisynthetic vitamin E actually contained 50% d,d,d-alpha tocopherol moiety and 50% l,d,d-alpha-tocopherol moiety, as synthesized by an earlier process which started with a plant sterol intermediate with the correct chirality in the tail, and thus resulted in a racemic mixture at only one chiral center. This form, known as 2-ambo tocopherol, is no longer made.)

Natural alpha-tocopherol is the RRR-alpha (or ddd-alpha) form. The synthetic dl,dl,dl-alpha ("dl-alpha") form is not as active as the natural ddd-alpha ("d-alpha") tocopherol form. This is mainly due to nearly complete vitamin inactivity of the 4 possible chiral alpha epimers which are represented by the "l" or "S" enantiomer at the first chiral center (an S or l configuration between the chromanol ring and the tail, i.e., the SRR, SRS, SSR, and SSS epimers). Unnatural 2R chiral forms with natural R configuration at this key center, but S at the other centers in the tail (RSR, RRS), appear to retain substantial RRR vitamin activity because they are recognized by the alpha tocopherol transport protein, and thus maintained in the plasma, where the other four epimers are not. Thus, the synthetic all-rac-α-tocopherol probably has only about half the vitamin activity of RRR-α-tocopherol in humans, even though the ratio of activities of the 8 isomer sythetic mixture to the natural vitamin is 1 to 1.36 in the rat pregnancy model. [9]

Although it is clear that synthetic form is not as active as the natural alpha tocopherol form, in the ratios discussed above, specific information on any side effects of the seven synthetic vitamin E epimers is not readily available. Naturopathic and orthomolecular medicine advocates have held that none of the synthetic vitamin E forms have merit for cancer, circulatory and heart diseases, but hold this opinion without being able to point to definitive studies of the matter.

Natural and Semi-synthetic

Semisynthetic "natural source" vitamin E, manufacturers convert the common natural beta, gamma and delta tocopherol isomers into the alpha form by adding methyl groups to yield d-alpha tocopherol. The largest manufacturers of this form are presently Cognis,Cargill and Archer Daniels Midland. Manufacturers also commonly convert the alcohol form of the vitamins to esters using acetic or succinic acid. These tocopheryl esters are more stable and are easy to use in tablets and multiple vitamin pills.

Because only alpha tocopherols were officially counted as "vitamin E" in supplements, refiners and manufacturers faced enormous economic pressure to esterify and methylate the other natural tocopherol isomers, d-beta-, d-gamma- and d-delta-tocopherol into d-alpha tocopheryl acetate or succinate. However, these alpha tocopheryl esters have been shown to be variably and less efficiently absorbed in humans than in the original normative tests using rats.[10] In the healthy human body, the semisynthetic forms are easily de-esterified over several days, primarily in the liver, but not for common problems in premature babies, aged or ill patients.

Tocopheryl nicotinate and tocopheryl linolate esters are used in cosmetics and some pharmaceuticals.

Mixed Tocopherols

"Mixed tocopherols" in the US contain at least 20% w/w other natural R, R,R- tocopherols, i.e. R, R,R-alpha-tocopherol content plus at least 25% R, R,R-beta-, R, R,R-gamma-, R, R,R-delta-tocopherols.

Some premium brands may contain 200% w/w or more of the other tocopherols and measurable tocotrienols. Some mixed tocopherols with higher gamma-tocopherol content are marketed as "High Gamma-Tocopherol". The label should report each component in milligrams, except R, R,R-alpha-tocopherol may still be reported in IU. Mixed tocopherols can also be found in various nutritional supplements manufactured by high end supplement companies.

Other Uses

Conventional medical studies on vitamin E, as of 2006 and as below, use either a synthetic all-racemic ("d, l-") alpha tocopheryl ester (acetate or succinate) or a semi-synthetic d-alpha tocopheryl ester (acetate or succinate). Proponents of megavitamin, orthomolecular and naturally based therapies have advocated, for the last two thirds of a century, and have used the natural tocopherols, often mixed tocopherols with an additional 25% - 200% w/w d-beta-, d-gamma-,[11][12] and d-delta-tocopherol. Based on various clinical, experimental, patent, and individual data, natural health proponents have long held[13][14] that the other poorly studied tocopherols, especially the abundant d-gamma-tocopherol,[15] in combination with other antioxidants such as selenium, coQ10, vitamin C, vitamin K2, mixed carotenoids, and lipoic acid, provide unique biochemical benefits.[16] The methodology, interpretation and reporting of conventional vitamin E studies have even become contentious within conventional medicine circles.[17]


"Megadoses" of Vitamin E are not recommended by many government agencies, due to a possible increased risk of bleeding. Two meta-analyses have concluded that synthetic and semisynthetic vitamin E supplements (alpha tocopheryl esters) increase mortality, although these meta-analyses have been repeatedly challenged in the nutrition literature for cofounders and selection bias.

A 2005 meta-analysis by Miller found that high-dosage vitamin E supplements may increase all-cause mortality.[18] "High dose" vitamin E esters (>400 units/day) were also associated with an increased risk in all-cause mortality of 39 per 10,000 persons, and a statistically significant relation existed between dose and mortality, with increased risk at doses exceeding 150 units per day. These trials included synthetic beta-carotene and other cofounders.

The Miller study was rebutted by Houston in the Journal of the American Nutraceutical Association.[16] Furthermore, Rosenberg concluded that "toxicity symptoms have not been reported even at intakes of 800 IU per kilogram of body weight daily for 5 months" according to the Food and Nutrition Board (Rosenberg, et al), an amount that corresponds to 60,000 IU per day for a 75 kg adult.

A review of a number of randomized controlled trials in the scientific literature by the Cochrane Collaboration published in JAMA in 2007 also found an increase in mortality, of 4% (Relative Risk 1.04, 95% confidence interval 1.01-1.07), or 400 per 10,000 persons.[19]

As a Preservative

Vitamin E is widely used in industry as an inexpensive preservative (namely for cosmetics and foods). Vitamin E containing products are commonly used in the belief that vitamin E is good for the skin; many cosmetics include it, often labeled as tocopherol acetate, tocopheryl linoleate or tocopheryl nicotinate. Individuals can still experience allergic reactions to some tocopheryl esters or develop a rash and hives that may spread over the entire body from the use of topical products with alpha tocopheryl esters.[20]

Reduce Scarring

Topical use of Vitamin E is often claimed by manufacturers of skin creams and lotions to play a role in encouraging skin healing and reducing scarring after injuries such as burns on the basis of limited research,[21] but the weak evidence of a benefit of silicon gel sheeting with or without added Vitamin E is limited by the poor quality of the research.[22] Indeed one study found that it did not improve or worsened the cosmetic appearance in 90% of patients, with a third developing contact dermatitis.[23]

During Pregnancy

Recent studies into the use of both vitamin C and the single isomer vitamin E esters as possible help in preventing oxidative stress leading to pre-eclampsia has failed to show significant benefits,[24] but did increase the rate of babies born with a low birthweight in one study.[25] However, earlier work that suggested vitamin K (similar structures to natural E isomers) and C together have 91% benefit in nausea and vomiting remains unaddressed.[26]

Heart Disease

Preliminary research has led to a widely held belief that vitamin E may help prevent or delay coronary heart disease, but larger controlled studies have not shown any benefit. Many researchers advance the belief that oxidative modification of LDL (also called "bad" cholesterol) promotes blockages in coronary arteries that may lead to atherosclerosis and heart attacks. Vitamin E may help prevent or delay coronary heart disease by limiting the oxidation of LDL. Vitamin E also may help prevent the formation of blood clots, which could lead to a heart attack. Observational studies have associated lower rates of heart disease with higher vitamin E intake. A study of approximately 90,000 nurses suggested that the incidence of heart disease was 30% to 40% lower among nurses with the highest intake of vitamin E from diet and supplements. The range of intakes from both diet and supplements in this group was 21.6 to 1,000 IU (32 to 1,500 mg), with the median intake being 208 IU (139 mg). A 1994 review of 5,133 Finnish men and women aged 30 - 69 years suggested that increased dietary intake of vitamin E was associated with decreased mortality (death) from heart disease.

But even though these observations are promising, randomized clinical trials have consistently shown lack of benefit to the role of vitamin E supplements in heart disease.

Supportive Trial Data

  • The Heart Outcomes Prevention Evaluation (HOPE) study followed almost 10,000 patients for 4.5 years who were at high risk for heart attack or stroke. In this intervention study the subjects who received 265 mg (400) IU of vitamin E daily did not experience significantly fewer cardiovascular events or hospitalizations for heart failure or chest pain when compared to those who received a sugar pill. The researchers suggested that it is unlikely that the vitamin E supplement provided any protection against cardiovascular disease in the HOPE study. The HOPE study was extended to evaluate whether long-term supplementation with vitamin E decreases the risk of cancer, cancer death, and major cardiovascular events (HOPE-The Ongoing Outcomes [HOPE-TOO]). Nearly 4500 patients were followed for a median time period of 7 years. This study did not find any significant differences in cancer incidence, cancer deaths, and major cardiovascular events, but found a higher rate of heart failure (17%) and hospitalizations for heart failure (21%) among the subjects.
  • The Women's Angiographic Vitamin and Estrogen trial was a randomized, double-blind, placebo-controlled study which enrolled 423 postmenopausal women with some degree of coronary stenosis, to study the efficacy of estrogen replacement and antioxidant vitamins (vitamin C and vitamin E) in preventing angiographic progression of coronary artery disease. The study reported no cardiovascular benefit in women taking supplements compared to those on placebo. Moreover all-cause mortality was significantly higher in women taking the supplements. [27][28]
  • The Women's Health study was a randomized, placebo-controlled, 2×2 factorial study in which 39,876 apparently healthy US women aged ≥45 years were enrolled to assess whether vitamin E supplementation decreases risks of cardiovascular disease and cancer among healthy women. All the women were randomly assigned to receive vitamin E or placebo and aspirin or placebo. After a mean follow-up period of 10.1 years, the study reported no significant benefit on the incidences of cardiovascular events, cancer and all-cause mortality in the group taking vitamin E. However a significant reduction of 24% was observed in cardiovascular mortality.[29]
  • The Physicians' Health Study II was a randomized, double-blind, placebo-controlled factorial trial designed to evaluate whether long-term vitamin E or vitamin C supplementation decreases the risk of major cardiovascular events among men. 14,641 US male physicians ≥50 years of age were enrolled in this study. The subjects were randomly assigned to receive either alternate day vitamin E and daily vitamin C or a placebo. After a mean follow-up of 8 years the study found that neither vitamin E nor vitamin C supplementation reduced the risk of major cardiovascular events.[30]

Furthermore, meta analysis of several trials of antioxidants, including vitamin E, have not shown any benefit to vitamin E supplementation for preventing coronary heart disease.[31] One study suggested that Vitamin E (as alpha-tocopherol only) supplementation may increase the risk for heart failure.[32] Supplementing alpha-tocopherol without gamma-tocopherol is known to lead to reduced serum gamma- and delta-tocopherol concentrations.[33]

Orthomolecular and naturopathic medicine use much different types of vitamin E, the natural mixed tocopherols, and other supportive cofactors such as, selenium, vitamin C, carnitine, lysine, and co-Q10 for various cardiovascular diseases.[34][35] See also Orthomolecular medicine:Vitamin E controversy.

On September 10, 2007, the American Heart Association (in its journal Circulation) stated that women taking regular doses of vitamin E or Tocopherol were 21% less likely to suffer a blood clot. Dr. Robert Glynn of Harvard Medical School said it was an interesting finding but not yet proven and further research must confirm the link in the prevention of venous thromboembolism, and patients must not stop taking prescribed blood thinners.[36]


Antioxidants such as vitamin E help protect against the damaging effects of free radicals, which may contribute to the development of chronic diseases such as cancer. Vitamin E also may block the formation of nitrosamines, which are carcinogens formed in the stomach from nitrites consumed in the diet. It also may protect against the development of cancers by enhancing immune function. To date, human trials and surveys that have tried to associate vitamin E with incidence of cancer remain generally inconclusive.

Some evidence associates higher intake of vitamin E with a decreased incidence of prostate cancer (see ATBC study) and breast cancer. Some studies correlate additional cofactors, such as specific vitamin E isomers, e.g. gamma-tocopherol, and other nutrients, e.g. selenium, with dramatic risk reductions in prostate cancer.[37] However, an examination of the effect of dietary factors, including vitamin E, on incidence of postmenopausal breast cancer in over 18,000 women from New York State did not associate a greater vitamin E intake with a reduced risk of developing breast cancer. A study of the effect on lung cancer in smokers also showed no benefit.[38]

A study of women in Iowa provided evidence that an increased dietary intake of vitamin E may decrease the risk of colon cancer, especially in women under 65 years of age. On the other hand, vitamin E intake was not statistically associated with risk of colon cancer in almost 2,000 adults with cancer who were compared to controls without cancer. At this time there is limited evidence to recommend vitamin E supplements for the prevention of cancer.

Recent studies have found that increased intake of vitamin E, especially among smokers may be responsible for an increase in the incidence of lung cancer, with one study finding an increase in the incidence of lung cancer by 7% for each 100IU of vitamin E taken daily.[39][40][41]


A cataract is a condition of clouding of the tissue of the lens of the eye. They increase the risk of disability and blindness in aging adults. Antioxidants are being studied to determine whether they can help prevent or delay cataract growth. Observational studies have found that lens clarity, which is used to diagnose cataracts, was better in regular users of vitamin E supplements and in persons with higher blood levels of vitamin E. A study of middle aged male smokers, however, did not demonstrate any effect from vitamin E supplements on the incidence of cataract formation. The effects of smoking, a major risk factor for developing cataracts, may have overridden any potential benefit from the vitamin E, but the conflicting results also indicate a need for further studies before researchers can confidently recommend extra vitamin E for the prevention of cataracts.

It is important to note that the term "cataract" may be used in common parlance for an opacity involving any tissue of the eye, for example a corneal scar. Thus a character in theater or on television who is blind from cataracts might have white instead of clear corneas, covering over the iris and pupil. Since the lens is behind the pupil, real cataracts are difficult to see without special instrumentation, so people with cataracts have rather normally appearing eyes.

Age-related Macular Degeneration (AMD)

Age-related macular degeneration (AMD) is the leading cause of visual impairment and blindness in the United States and the developed world among people 65 years and older. It has been shown that vitamin E alone does not attenuate the development or progression of AMD.[42]

However, studies focusing on efficacy of Vitamin E combined with other antioxidants, like zinc and vitamin C, indicate a protective effect against the onset and progression of AMD[43][44][45]


A 2007 study published in the European Journal of Ophthalmology found that, along with other treatments for glaucoma, adding alpha-tocopherol appeared to help protect the retina from glaucomatous damage. Groups receiving 300 mg and 600 mg per day of alpha-tocopherol, delivered orally, showed statistically significant decreases in the resistivity index in the posterior ciliary arteries and in the pulsatility index in the ophthalmic arteries, after six and twelve months of therapy. Alpha-tocopherol-treated patients also had significantly lower differences in mean visual field deviations."[46]

Alzheimer's Disease

Alzheimer's disease is a wasting disease of the brain. As oxidative stress may be involved in the pathogenesis of Alzheimer's, tocopherols have been tested as both a means of preventing and treating this disease. The results of these studies have been mixed, with some research suggesting that high levels of vitamin E in the diet may reduce the risk of Alzheimer's, while other studies found no such link.[47] Similarly, studies on if tocopherols could slow the progression of Alzheimer's have also been contradictory, with the Alzheimer’s Disease Cooperative Study suggesting that vitamin E supplementation might be beneficial, but a later trial finding no clinical benefit.[48] Due to this contradictory and confusing evidence, vitamin E or tocopherol supplements are not currently recommended for treating or preventing Alzheimer's disease.[49]

Parkinson's Disease

In May 2005, The Lancet Neurology published a study suggesting that vitamin E may help protect against Parkinson's disease.[50] Individuals with moderate to high intakes of dietary vitamin E were found to have a lower risk of Parkinson's. No conclusion was drawn about whether supplemental vitamin E has the same effect, however.[51]

Related Chapters

  • Alkylresorcinols

External Links


  1. Burton, G. W. and Ingold, K. U., "Autoxidation of biological molecules. 1. Antioxidant activity of vitamin E and related chain-breaking phenolic antioxidants in vitro", J. Am. Chem. Soc., 1981, 103, 6472 - 6477.
  2. Composition of Foods Raw, Processed, Prepared USDA National Nutrient Database for Standard Reference, Release 20 USDA, Feb. 2008
  3. Evans H. M., Bishop K. S. (1922). "On the existence of a hitherto unrecognized dietary factor essential for reproduction". Science. 56 (1458): 650–651. doi:10.1126/science.56.1458.650.
  4. Evans H. M., Emerson O. H., Emerson G. A. (1936). "The isolation from wheat germ oil of an alcohol, a-tocopherol, having the properties of vitamin E". Journal of Biological Chemistry. 113 (1): 319–332.
  5. Fernholz E. (1938). "On the Constitution of α-Tocopherol". Journal of the American Chemical Society. 60 (1): 700–705. doi:10.1021/ja01270a057.
  6. L. Iuliano; F. Micheletta; M. Maranghi; G. Frati; U. Diczfalusy; F. Violi (2001). "Bioavailability of Vitamin E as Function of Food Intake in Healthy Subjects". Arteriosclerosis, Thrombosis, and Vascular Biology. 21: e34&ndash, e37. doi:10.1161/hq1001.098465. PMID 11597949.
  7. Vitamin E Fact sheet
  8. J. Bauernfeind in: L. J. Machlin (ed.): Vitamin E – A Comprehensive Treatise, Marcel Dekker, New York 1980, p. 99
  9. "Taken together, these data indicate that of the eight stereoisomers (RRR, RSR, RRS, RSS, SRR, SSR, SRS, SSS) in all-rac-α-tocopherol, only the four 2R-forms (RRR, RSR, RSS, RRS) are recognized by α-TTP and maintained in the plasma. Indeed, the Food and Nutrition Board (Food and Nutrition Board and Institute of Medicine, 2000) has defined that only α-tocopherol, specifically the 2R-forms of α-tocopherol, can fulfill the human requirement for vitamin E. Thus, all-rac-α-tocopherol has only half the activity of RRR-α-tocopherol." Taken from the discussion in [1]: Relative bioactivity of dietary RRR- and all-rac-alpha-tocopheryl acetates in swine assessed with deuterium-labeled vitamin E1. J Anim Sci 80:702-707, 2002.
  10. Horwitt M, Elliott W, Kanjananggulpan P, Fitch C (1984). "Serum concentrations of alpha-tocopherol after ingestion of various vitamin E preparations". Am J Clin Nutr. 40 (2): 240–5. PMID 6465056. link
  11. Jiang Q et al."Gamma tocopherol, the major form of vitamin E in the US diet, deserves more attention" Am J Clin Nutr 2001; 74: 714-22.
  12. JM Gaziano, Vitamin E and Cardiovascular Disease: Observational Studies, Ann. N.Y. Acad. Sci. 1031: 280–291 (2004) "
  13. Bailey H (1964) Vitamin E: Your Key to a Healthy Heart, Chilton Books, ASIN B000GS9VPQ Bailey describes mixed tocopherols use for CVD back to the 1940s
  14. Walker M, "New/Old Findings on Unique Vitamin E", Townsend Letter for Doctors and Patients, No. 111, 1992, p. 826
  15. MacWilliam L,"What Makes Gamma Tocopherol Superior to Alpha Tocopherol", LE Magazine, Report, April 2006
  16. 16.0 16.1 M. Houston, “Meta-Analysis, Metaphysics and Mythology” JANA Vol. 8 No. 1, 2005 original
  17. Carter, T. "Responses and Comments: High-Dosage Vitamin E Supplementation and All-Cause Mortality", Ann Intern Med. 2005 July 19;143(2):155; responses 150-160
  18. Miller E, Pastor-Barriuso R, Dalal D, Riemersma R, Appel L, Guallar E (2005). "Meta-analysis: high-dosage vitamin E supplementation may increase all-cause mortality". Ann Intern Med. 142 (1): 37–46. PMID 15537682.
  19. Bjelakovic et al., "Mortality in randomized trials of antioxidant supplements for primary and secondary prevention: Systematic review and meta-analysis", JAMA, 297:842; February 28, 2007 [2]
  20. Topical Vitamin E Formulations: Not Always Benign, Skin Therapy Letter Vol. 1, No. 3, January 1996
  21. Palmieri B, Gozzi G, Palmieri G (1995). "Vitamin E added silicone gel sheets for treatment of hypertrophic scars and keloids". Int. J. Dermatol. 34 (7): 506–9. doi:10.1111/j.1365-4362.1995.tb00628.x. PMID 7591421.
  22. O'Brien L, Pandit A (2006). "Silicon gel sheeting for preventing and treating hypertrophic and keloid scars". Cochrane Database Syst Rev (1): CD003826. doi:10.1002/14651858.CD003826.pub2. PMID 16437463.
  23. Baumann LS, Spencer J (1999). "The effects of topical vitamin E on the cosmetic appearance of scars". Dermatol Surg. 25 (4): 311–5. doi:10.1046/j.1524-4725.1999.08223.x. PMID 10417589. Lay summaryVitamin E - Paula Begoun at CosmeticsCop (2008-01-01).
  24. Rumbold A, Crowther C, Haslam R, Dekker G, Robinson J (2006). "Vitamins C and E and the risks of pre-eclampsia and perinatal complications". N Engl J Med. 354 (17): 1796–806. doi:10.1056/NEJMoa054186. PMID 16641396.
  25. Poston L, Briley A, Seed P, Kelly F, Shennan A (2006). "Vitamin C and vitamin E in pregnant women at risk for pre-eclampsia (VIP trial): randomised placebo-controlled trial". Lancet. 367 (9517): 1145–54. doi:10.1016/S0140-6736(06)68433-X. PMID 16616557.
  26. Pizzorno JE, Murray MT (November 2005) Textbook of Natural Medicine, 3rd edition, Churchill Livingstone, ISBN 0-443-07300-7, pg 1942 Vitamin K and C, when used together, have shown considerable clinical efficacy, with 91% of patients in one study showing complete remission of nausea and vomiting within 72 hours. Both vitamins alone show little effect.
  27. Hsia J, Alderman EL, Verter JI; et al. (2002). "Women's angiographic vitamin and estrogen trial: design and methods". Controlled Clinical Trials. 23 (6): 708–27. PMID 12505248. Unknown parameter |month= ignored (help)
  28. Waters DD, Alderman EL, Hsia J; et al. (2002). "Effects of hormone replacement therapy and antioxidant vitamin supplements on coronary atherosclerosis in postmenopausal women: a randomized controlled trial". JAMA : the Journal of the American Medical Association. 288 (19): 2432–40. PMID 12435256. Unknown parameter |month= ignored (help)
  29. Lee IM, Cook NR, Gaziano JM; et al. (2005). "Vitamin E in the primary prevention of cardiovascular disease and cancer: the Women's Health Study: a randomized controlled trial". JAMA : the Journal of the American Medical Association. 294 (1): 56–65. doi:10.1001/jama.294.1.56. PMID 15998891. Unknown parameter |month= ignored (help)
  30. Sesso HD, Buring JE, Christen WG; et al. (2008). "Vitamins E and C in the prevention of cardiovascular disease in men: the Physicians' Health Study II randomized controlled trial". JAMA : the Journal of the American Medical Association. 300 (18): 2123–33. doi:10.1001/jama.2008.600. PMC 2586922. PMID 18997197. Unknown parameter |month= ignored (help)
  31. Vivekananthan D, Penn M, Sapp S, Hsu A, Topol E (2003). "Use of antioxidant vitamins for the prevention of cardiovascular disease: meta-analysis of randomised trials". Lancet. 361 (9374): 2017–23. doi:10.1016/S0140-6736(03)13637-9. PMID 12814711.
  32. Lonn E, Bosch J, Yusuf S, Sheridan P, Pogue J, Arnold J, Ross C, Arnold A, Sleight P, Probstfield J, Dagenais G (2005). "Effects of long-term vitamin E supplementation on cardiovascular events and cancer: a randomized controlled trial". JAMA. 293 (11): 1338–47. PMID 15769967.
  33. Huang HY, Appel LJ (2003). "Supplementation of diets with alpha-tocopherol reduces serum concentrations of gamma- and delta-tocopherol in humans". J. Nutr. 133 (10): 3137–40. PMID 14519797.
  34. Saul A. "Shute Vitamin E Treatment Protocol".
  35. Saul A. "Congestive Heart Failure", 2003.
  36., Vitamin E may reduce blood clots in women: study
  37. Helzlsouer K, Huang H, Alberg A, Hoffman S, Burke A, Norkus E, Morris J, Comstock G (2000). "Association between alpha-tocopherol, gamma-tocopherol, selenium, and subsequent prostate cancer". J Natl Cancer Inst. 92 (24): 2018–23. doi:10.1093/jnci/92.24.2018. PMID 11121464.
  38. "The effect of vitamin E and beta carotene on the incidence of lung cancer and other cancers in male smokers. The Alpha-Tocopherol, Beta Carotene Cancer Prevention Study Group". N Engl J Med. 330 (15): 1029–35. 1994. PMID 8127329.
  39. Cancer Research UK : Jury still out over vitamin E supplements and increased lung cancer risk
  40. Nursing in Practice - Vitamin E "linked to cancer"
  41. - Vitamin E Linked To Increased Risk of Lung Cancer
  42. Taylor H, Tikellis G, Robman L, McCarty C, McNeil J (2002). "Vitamin E supplementation and macular degeneration: randomised controlled trial". BMJ. 325 (7354): 11. doi:10.1136/bmj.325.7354.11. PMID 12098721.
  43. "A randomized, placebo-controlled, clinical trial of high-dose supplementation with vitamins C and E, beta carotene, and zinc for age-related macular degeneration and vision loss: AREDS report no. 8". Arch Ophthalmol. 119 (10): 1417–36. 2001. PMID 11594942.
  44. van Leeuwen R, Boekhoorn S, Vingerling J, Witteman J, Klaver C, Hofman A, de Jong P (2005). "Dietary intake of antioxidants and risk of age-related macular degeneration". JAMA. 294 (24): 3101–7. PMID 16380590.
  45. Moriarty-Craige S, Adkison J, Lynn M, Gensler G, Bressler S, Jones D, Sternberg P (2005). "Antioxidant supplements prevent oxidation of cysteine/cystine redox in patients with age-related macular degeneration". Am J Ophthalmol. 140 (6): 1020–6. PMID 16376645.
  46. Engin KN, Engin G, Kucuksahin H, Oncu M, Engin G, Guvener B (2007). "Clinical evaluation of the neuroprotective effect of alpha-tocopherol against glaucomatous damage". European journal of ophthalmology. 17 (4): 528–33. PMID 17671926.
  47. Frank B, Gupta S (2005). "A review of antioxidants and Alzheimer's disease". Ann Clin Psychiatry. 17 (4): 269–86. doi:10.1080/10401230500296428. PMID 16402761.
  48. Ricciarelli R, Argellati F, Pronzato MA, Domenicotti C (2007). "Vitamin E and neurodegenerative diseases". Mol. Aspects Med. 28 (5–6): 591–606. doi:10.1016/j.mam.2007.01.004. PMID 17306357.
  49. Boothby LA, Doering PL (2005). "Vitamin C and vitamin E for Alzheimer's disease". Ann Pharmacother. 39 (12): 2073–80. doi:10.1345/aph.1E495. PMID 16227450. Unknown parameter |month= ignored (help)
  50. Etminan M, Gill SS, Samii A (2005). "Intake of vitamin E, vitamin C, and carotenoids and the risk of Parkinson's disease: a meta-analysis". Lancet Neurol. 4 (6): 362–5. doi:10.1016/S1474-4422(05)70097-1. PMID 15907740.
  51. "Vitamin E cuts Parkinson's risk". BBC News. 19 May, 2005. Retrieved 2008-01-01. Check date values in: |date= (help)

ca:Vitamina E cs:Tokoferol da:Vitamin E de:Tocopherol eo:Vitamino E et:E-vitamiin eu:E bitamina fa:ویتامین ای fi:E-vitamiini he:ויטמין E hr:Vitamin E it:Tocoferolo ko:바이타민 E lt:Vitaminas E nl:Vitamine E sh:Vitamin E simple:Vitamin E sl:Vitamin E sv:Alfatokoferol ta:உயிர்ச்சத்து E th:วิตามินอี uk:Токоферол Template:Jb1

Template:WikiDoc Sources