Vitamin E is an antioxidant that protects
cell membranes and other fat-soluble parts of the body, such as low-density lipoprotein (LDL;
“bad” cholesterol) cholesterol,
from damage.
Where is it found?
Wheat germ oil, nuts and seeds, whole grains, egg yolks, and leafy green vegetables all contain vitamin E. Certain
vegetable oils should contain significant
amounts of vitamin E. However, many of the vegetable oils sold in supermarkets have had the
vitamin E removed in processing. The high amounts found in supplements, often 100 to 800 IU
per day, are not obtainable from eating food.
Vitamin E has been used in
connection with the following conditions (refer to the individual
health concern for complete information):
Reliable
and relatively consistent scientific data showing a substantial health benefit. Contradictory, insufficient, or preliminary studies
suggesting a health benefit or minimal health benefit. For an herb, supported by traditional use but minimal
or no scientific evidence. For a supplement, little scientific support and/or minimal health
benefit.
Who is likely to be deficient?
Severe vitamin E deficiencies are rare. People with a genetic defect in a vitamin E
transfer protein called thrombotic thrombocytopenic purpura (TTP) have severe vitamin E
deficiency, characterized by low blood and tissue levels of vitamin E and progressive nerve
abnormalities.12
Low vitamin E status has been associated with an increased risk of rheumatoid arthritis3 and major depression.4 Women with preeclampsia have been found to have lower blood
levels of vitamin E than women without the condition.5
Very old people with type 2 diabetes have
shown a significant age-related decline in blood levels of vitamin E, irrespective of their
dietary intake.6
Which form is best?
The names of all types of vitamin E begin with either “d” or “dl,”
which refer to differences in chemical structure. The “d” form is natural (also
known as RRR-alpha tocopherol) and “dl” is synthetic (more correctly
known as all-rac-alpha tocopherol). The natural form is more active and better absorbed.
Little is known about how the “unnatural” “l” portion of the synthetic
“dl” form affects the body, though no clear toxicity has been discovered.
In theory, when a vitamin E supplement is labeled “400 IU” it should have the
same level of activity regardless of its source. This is purportedly achieved by using more
synthetic vitamin E to reach the same potency as a lesser amount of natural vitamin E. For
example, 100 IU of vitamin E requires about 67 mg of the natural form but closer to 100 mg of
the synthetic. However, a recent review of the scientific evidence suggests that natural
vitamin E probably has greater activity in the body than indicated on the label.7
Natural vitamin E may be as much as twice as bioavailable as synthetic vitamin E, not 1.36
times as is generally accepted.8 Many doctors advise people to use only the
natural, the “d” form, of vitamin E.
After the “d” or “dl” designation, often the Greek letter
“alpha” appears, which also describes the structure. Synthetic “dl”
vitamin E is found only in the alpha form—as in “dl-alpha tocopherol.”
Natural vitamin E may be found either as alpha—as in “d-alpha
tocopherol”—or in combination with beta, gamma, and delta, labeled
“mixed”—as in mixed natural tocopherols.
Little is known about the importance of the beta and delta forms of vitamin E, but a debate
has arisen concerning gamma tocopherol. In a test tube study, gamma tocopherol was found to be
more effective than alpha tocopherol in protecting against certain specific types of oxidative
damage.9 In addition, some research has shown that supplementation with large
amounts of alpha tocopherol (such as 1,200 IU per day) increases the breakdown, and decreases
blood levels, of gamma tocopherol.10
Human trials with vitamin E have almost always been done with the alpha (not gamma) form.
Historically the synthetic “dl” form was used in most trials, but some trials are
now using the natural form. The issue of alpha vs. gamma form requires more research before it
can be fully understood.
Almost all vitamin E research shows that, when positive results are obtained, hundreds of
units per day are required—an amount easily obtained with supplements but impossible
with food. Therefore, switching to food sources, as suggested by some researchers, is
impractical. On the other hand, the vitamin E occurring naturally in food contains gamma
tocopherol and other tocopherols. Thus, it possibly may turn out to be more effective than the
vitamin E taken in supplement form. Additional research is needed in this area.
Vitamin E forms are listed as either plain “tocopherol” or tocopheryl followed
by the name of what is attached to it, as in “tocopheryl acetate.” The two forms
are not greatly different. However, plain tocopherol may be absorbed a little better, while
tocopheryl attached forms have a slightly better shelf life. Both forms are active when taken
by mouth. However, the skin utilizes the tocopheryl forms very slowly,11
12 so those planning to apply vitamin E to the skin should buy plain tocopherol. In
health food stores, the most common forms of vitamin E are d-alpha tocopherol and d-alpha
tocopheryl acetate or succinate. Both of these d (natural) alpha forms are frequently
recommended by doctors. Although the succinate form is slightly weaker than the acetate form,
more milligrams of the succinate form are added to supplements to compensate for this small
difference in potency. Therefore, 400 IU of either form should have equivalent potency.
How much is usually taken?
The recommended dietary allowance for vitamin E is low, just 15 mg or approximately 22
International Units (IU) per day. The most commonly recommended amount of supplemental vitamin
E for adults is 400 to 800 IU per day. However, some leading researchers suggest taking only
100 to 200 IU per day, since trials that have explored the long-term effects of different
supplemental levels suggest no further benefit beyond that amount. In addition, research
reporting positive effects with 400 to 800 IU per day has not investigated the effects of
lower intakes.13 For tardive
dyskinesia, the best results have been achieved from 1,600 IU per day,14 a
large amount that should be supervised by a healthcare practitioner.
Are there any side effects or interactions?
Vitamin E toxicity is very rare and supplements are widely considered to be safe. The
National Academy of Sciences has established the daily tolerable upper intake level for adults
to be 1,000 mg of vitamin E, which is equivalent to 1,500 IU of natural vitamin E or 1,100 IU
of synthetic vitamin E.15
In a double-blind study of healthy elderly people, supplementation with 200 IU of vitamin E
per day for 15 months had no effect in the incidence of respiratory infections, but increased
the severity of those infections that did occur.16 For elderly individuals, the
risks and benefits of taking this vitamin should be assessed with the help of a doctor or
nutritionist.
In contrast to trials suggesting vitamin E improves glucose tolerance in people with diabetes, one trial reported that 600 IU per day
of vitamin E led to impairment in glucose tolerance in obese people with
diabetes.17 The reason for the discrepancy between reports is not known.
In a double-blind study of people with established heart disease or diabetes, participants who took 400 IU of vitamin E
per day for an average of 4.5 years developed
heart failure significantly more often than did those taking a placebo.18
Hospitalizations for heart failure occurred in 5.8% of those in the vitamin E group, compared
with 4.2% of those in the placebo group, a 38.1% increase. Considering that some other studies
have shown a beneficial effect of vitamin E against heart disease, the results of this study
are difficult to interpret. Nevertheless, individuals with heart disease or diabetes should
consult their doctor before taking vitamin E.
A review of 19 clinical trials of vitamin E supplementation concluded that long-term use of
large amounts of vitamin E (400 IU per day or more) was associated with a small (4%) but
statistically significant increase in risk of death.19 Long-term use of less than
400 IU per day was associated with a small and statistically nonsignificant reduction in death
rates. This research has been criticized because many of the studies on which it was based
used a combination of nutritional supplements, not just vitamin E. For example, the adverse
effects reported in some of the studies may have been due to the use of large amounts of zinc
or synthetic beta-carotene, and may have had nothing to do with vitamin E. It is also possible
that long-term use of large amounts of pure alpha-tocopherol may lead to a deficiency of
gamma-tocopherol, with potential negative consequences. For that reason, some doctors
recommend that people who need to take large amounts of vitamin E take at least part of it in
the form of mixed tocopherols.
Patients on kidney dialysis who are given injections of iron frequently experience “oxidative
stress.” This is because iron is a pro-oxidant, meaning that it interacts with oxygen
molecules in ways that may damage tissues. These adverse effects of iron therapy may be
counteracted by supplementation with vitamin E.20
A diet high in unsaturated fat increases vitamin E requirements. Vitamin E and selenium work together to protect fat-soluble parts of
the body.
Are there any drug
interactions?
Certain medicines may interact with vitamin E. Refer to drug interactions for a list of those medicines.
References (To view, roll mouse over the "References" heading; to hide, click on the heading)
1. Traber MG. Vitamin E. In: Shils ME, Olsen JA, Shike M, Ross AC (eds).
Modern Nutrition in Health and Disease. Baltimore: Williams & Wilkins, 1999,
347–62.
2. Cavalier L, Ouahchi K, Kayden HJ, et al. Ataxia with isolated vitamin
E deficiency: heterogeneity of mutations and phenotypic variability in a large number of
families. Am J Hum Genet 1998;62:301–10.
3. Knekt P, Heliovaara M, Aho K, et al. Serum selenium, serum
alpha-tocopherol, and the risk of rheumatoid arthritis. Epidemiology
2000;11:402–5.
4. Maes M, De Vos N, Pioli R, et al. Lower serum vitamin E concentrations
in major depression. Another marker of lowered antioxidant defenses in that illness. J
Affect Disord 2000;58:241–6.
5. Kharb S. Total free radical trapping antioxidant potential in
pre-eclampsia. Int J Gynaecol Obstet 2000;69:23–6.
6. Polidori MC, Mecocci P, Stahl W, et al. Plasma levels of lipophilic
antioxidants in very old patients with type 2 diabetes. Diabetes Metab Res Rev
2000;16:15–9.
7. VERIS Research Information Service. Summary finds superiority of
natural vitamin E supplements over synthetic forms. Townsend Letter for Doctors &
Patients 1999;July:100–5 [review].
8. Acuff RV, Thedford SS, Hidiroglou NN, et al. Relative bioavailability
of RRR- and all-rac-alpha-tocopheryl acetate in humans: studies using deuterated compounds.
Am J Clin Nutr 1994;60:397–402.
9. Christen S, Woodall AA, Shigenaga MK, et al. Gamma-tocopherol traps
mutagenic electrophiles such as NO+ and complements alpha-tocopherol: physiological
implications. Proc Natl Acad Sci 1997;94:3217–22.
10. Morinobu T, Yoshikawa S, Hamamura K, Tamai H. Measurement of vitamin
E metabolites by high-performance liquid chromatography during high-dose administration of
alpha-tocopherol. Eur J Clin Nutr 2003;57:410–4.
11. Beijersbergen van Henegouwen GM, Junginger HE, de Vries H. Hydrolysis
of RRR-alpha-tocopheryl acetate (vitamin E acetate) in the skin and its UV protecting activity
(an in vivo study with the rat). J Photochem Photobiol B 1995;29:45–51.
12. Norkus EP, Bryce GF, Bhagavan HN. Uptake and bioconversion of
alpha-tocopheryl acetate to alpha-tocopherol in skin of hairless mice. Photochem
Photobiol 1993;57:613–5.
13. Rimm E. Micronutrients, coronary heart disease and cancer: should we
all be on supplements? Presented at the 60th Annual Biology Colloquium, Oregon State
University, February 25, 1999.
14. Hashim S, Sajjad A. Vitamin E in the treatment of tardive dyskinesia:
a preliminary study over 7 months at different doses. Int Clin Psychopharmacol
1988;13:147–55.
15. Panel on Dietary Antioxidants and Related Compounds, Food and
Nutrition Board, Institute of Medicine, National Academy of Sciences. Dietary Reference
Intakes for Vitamin C, Vitamin E, Selenium, and Carotenoids. Washington, D.C.: National
Academy Press, 2000, 249–59.
16. Graat JM, Schouten EG, Kok FJ. Effect of daily vitamin E and
multivitamin-mineral supplementation on acute respiratory tract infections in elderly persons:
a randomized controlled trial. JAMA 2002;288:715–21.
17. Skrha J, Sindelka G, Kvasnicka J, Hilgertova J. Insulin action and
fibrinolysis influenced by vitamin E in obese type 2 diabetes mellitus. Diabetes Res Clin
Pract 1999;44:27–33.
18. Zoler ML. Supplemental vitamin E linked to heart failure. Fam
Pract News 2003 (October 1):28 [News report].
19. Miller ER III, Pastor-Barriuso R, Dalal D, et al. Meta-analysis:
high-dosage vitamin E supplementation may increase all-cause mortality. Ann Intern
Med 2005;142:37–46.
20. Roob JM, Khoschsorur G, Tiran A, et al. Vitamin E attenuates
oxidative stress induced by intravenous iron in patients on hemodialysis. J Am Soc
Nephrol 2000;11:539–49.
The information presented in Healthnotes is for informational purposes
only. It is based on scientific studies (human, animal, or in vitro), clinical
experience, or traditional usage as cited in each article. The results reported may not
necessarily occur in all individuals. For many of the conditions discussed, treatment with
prescription or over the counter medication is also available. Consult your doctor,
practitioner, and/or pharmacist for any health problem and before using any supplements or
before making any changes in prescribed medications. Information expires September 2008.