What is selenium?Selenium is a trace mineral that is
essential to good health but required only in small amounts [1,2].
Selenium is incorporated into proteins to make selenoproteins, which
are important antioxidant enzymes. The antioxidant properties of
selenoproteins help prevent cellular damage from free radicals. Free
radicals are natural by-products of oxygen metabolism that may
contribute to the development of chronic diseases such as cancer and
heart disease [2,3].
Other selenoproteins help regulate thyroid function and play a role
in the immune system [4-7].
What foods provide selenium?Plant foods are the major
dietary sources of selenium in most countries throughout the world.
The content of selenium in food depends on the selenium content of
the soil where plants are grown or animals are raised. For example,
researchers know that soils in the high plains of northern Nebraska
and the Dakotas have very high levels of selenium. People living in
those regions generally have the highest selenium intakes in the
United States (U.S.) [8]. In
the U.S., food distribution patterns across the country help prevent
people living in low-selenium geographic areas from having low
dietary selenium intakes. Soils in some parts of China and Russia
have very low amounts of selenium. Selenium deficiency is often
reported in those regions because most food in those areas is grown
and eaten locally.
Selenium also can be found in some meats
and seafood. Animals that eat grains or plants that were grown in
selenium-rich soil have higher levels of selenium in their muscle.
In the U.S., meats and bread are common sources of dietary selenium
[9,10].
Some nuts are also sources of selenium.
Selenium content of
foods can vary. For example, Brazil nuts may contain as much as 544
micrograms of selenium per ounce. They also may contain far less
selenium. It is wise to eat Brazil nuts only occasionally because of
their unusually high intake of selenium. Selected food sources of
selenium are provided in Table 1 [11].
Table
1: Selected food sources of selenium [11]
| Food |
Micrograms (μg) |
Percent DV* |
| Brazil nuts, dried, unblanched, 1 ounce |
544 |
780 |
| Tuna, light, canned in oil, drained, 3 ounces |
63 |
95 |
| Beef, cooked, 3½ ounces |
35 |
50 |
| Spaghetti w/ meat sauce, frozen entrée, 1 serving |
34 |
50 |
| Cod, cooked, 3 ounces |
32 |
45 |
| Turkey, light meat, roasted, 3½ ounces |
32 |
45 |
| Beef chuck roast, lean only, roasted, 3 ounces |
23 |
35 |
| Chicken Breast, meat only, roasted, 3½ ounces |
20 |
30 |
| Noodles, enriched, boiled, 1/2 cup |
17 |
25 |
| Macaroni, elbow, enriched, boiled, 1/2 cup |
15 |
20 |
| Egg, whole, 1 medium |
14 |
20 |
| Cottage cheese, low fat 2%, 1/2 cup |
12 |
15 |
| Oatmeal, instant, fortified, cooked, 1 cup |
12 |
15 |
| Rice, white, enriched, long grain, cooked, 1/2 cup |
12 |
15 |
| Rice, brown, long-grained, cooked, 1/2 cup |
10 |
15 |
| Bread, enriched, whole wheat, commercially prepared, 1
slice |
10 |
15 |
| Walnuts, black, dried, 1 ounce |
5 |
8 |
| Bread, enriched, white, commercially prepared, 1 slice |
4 |
6 |
| Cheddar cheese, 1 ounce |
4 |
6 | *DV = Daily Value.
DVs are reference numbers developed by the Food and Drug
Administration (FDA) to help consumers determine if a food contains
a lot or a little of a specific nutrient. The DV for selenium is 70
micrograms (ug). Most food labels do not list a food's selenium
content. The percent DV (%DV) listed on the table indicates the
percentage of the DV provided in one serving. A food providing 5% of
the DV or less is a low source while a food that provides 10-19% of
the DV is a good source. A food that provides 20% or more of the DV
is high in that nutrient. It is important to remember that foods
that provide lower percentages of the DV also contribute to a
healthful diet. For foods not listed in this table, please refer to
the U.S. Department of Agriculture's Nutrient Database Web site: http://www.nal.usda.gov/fnic/cgi-bin/nut_search.pl.
What is the recommended dietary intake for
selenium?Recommendations for selenium are provided in the
Dietary Reference Intakes developed by the Institute of Medicine [12].
Dietary Reference Intakes (DRIs) is the general term for a
set of reference values used for planning and assessing nutrient
intake for healthy people. Three important types of reference values
included in the DRIs are Recommended Dietary Allowances
(RDA), Adequate Intakes (AI), and Tolerable Upper
Intake Levels (UL). The RDA recommends the average daily
dietary intake level that is sufficient to meet the nutrient
requirements of nearly all (97-98%) healthy individuals in each age
and gender group [12].
An AI is set when there is insufficient scientific data available to
establish a RDA. AIs meet or exceed the amount needed to maintain a
nutritional state of adequacy in nearly all members of a specific
age and gender group. The UL, on the other hand, is the maximum
daily intake unlikely to result in adverse health effects [12].
Table 2 lists the RDAs for selenium, in micrograms (μg) per day, for
children and adults.
Table 2: Recommended Dietary
Allowances (RDA) for selenium for children and adults [12]
Age (years) |
Males and Females (μg/day) |
Pregnancy (μg/day) |
Lactation (μg/day) |
| 1-3 y |
20 |
N/A |
N/A |
| 4-8 y |
30 |
N/A |
N/A |
| 9-13 y |
40 |
N/A |
N/A |
| 14-18 y |
55 |
60 |
70 |
| 19 y + |
55 |
60 |
70 |
There is
insufficient information on selenium to establish a RDA for infants.
An Adequate Intake (AI) has been established that is based on the
amount of selenium consumed by healthy infants who are fed breast
milk [12].
Table 3 lists the AIs for selenium, in micrograms (μg) per day, for
infants.
Table 2: Adequate Intake for selenium for
infants [12]
Age (months) |
Males and Females (μg/day) |
| 0-6 months |
15 |
| 7-12 months |
20 |
Results of the
National Health and Nutrition Examination Survey (NHANES
III-1988-94) indicated that diets of most Americans provide
recommended amounts of selenium [13].
The INTERMAP study examined nutrient intakes of almost 5,000
middle-aged men and women in four countries in the late 1990s,
including the U.S. The primary aim of the study was to evaluate the
effect of dietary micronutrients on blood pressure. Each study
participant completed four, 24-hour dietary recalls, during which
they were asked to record everything consumed (food, beverages, and
dietary supplements) over the previous 24 hours. Selenium intake was
lowest among residents of China, the country with the highest known
rate of selenium deficiency. Mean dietary intake of selenium of U.S.
participants was 153 μg for men and 109 μg for women. Both values
exceed the recommended selenium intake for adults and are further
evidence of adequate selenium intakes in the U.S. [14].
When can selenium deficiency occur?Human selenium
deficiency is rare in the U.S. but is seen in other countries, most
notably China, where soil concentration of selenium is low [15].
There is evidence that selenium deficiency may contribute to
development of a form of heart disease, hypothyroidism, and a
weakened immune system [16,17].
There is also evidence that selenium deficiency does not usually
cause illness by itself. Rather, it can make the body more
susceptible to illnesses caused by other nutritional, biochemical or
infectious stresses [18].
Three specific diseases have been associated with selenium
deficiency:
Keshan Disease, which results in an enlarged heart and poor
heart function, occurs in selenium deficient children.
Kashin-Beck Disease, which results in osteoarthropathy
Myxedematous Endemic Cretinism, which results in mental
retardation
Keshan disease was first described in the early
1930s in China, and is still seen in large areas of the Chinese
countryside with selenium poor soil [18].
Dietary intake in these areas is less than 19 micrograms per day for
men and less than 13 micrograms per day for women, significantly
lower than the current RDA for selenium [12].
Researchers believe that selenium deficient people infected with a
specific virus are most likely to develop Keshan disease [18,19].
Selenium
deficiency has also been seen in people who rely on total parenteral
nutrition (TPN) as their sole source of nutrition [20,21].
TPN is a method of feeding nutrients through an intravenous (IV)
line to people whose digestive systems do not function. Forms of
nutrients that do not require digestion are dissolved in liquid and
infused through the IV line. It is important for TPN solutions to
provide selenium in order to prevent a deficiency [22].
Physicians can monitor the selenium status of individuals receiving
TPN to make sure they are receiving adequate amounts.
Severe
gastrointestinal disorders may decrease the absorption of selenium,
resulting in selenium depletion or deficiency [23].
Gastrointestinal problems that impair selenium absorption usually
affect absorption of other nutrients as well, and require routine
monitoring of nutritional status so that appropriate medical and
nutritional treatment can be provided.
Who may need supplemental selenium?In the U.S., most
cases of selenium depletion or deficiency are associated with severe
gastrointestinal problems, such as Crohn's disease, or with surgical
removal of part of the stomach. These and other gastrointestinal
disorders can impair selenium absorption [24-26].
People with acute severe illness who develop inflammation and
widespread infection often have decreased levels of selenium in
their blood [27].
Physicians will evaluate individuals who have gastrointestinal
disease or severe infection for depleted blood levels of selenium to
determine the need for supplementation.
People with iodine
deficiency may also benefit from selenium supplementation. Iodine
deficiency is rare in the U.S., but is still common in developing
countries where access to iodine is limited [28].
Researchers believe that selenium deficiency may worsen the effects
of iodine deficiency on thyroid function, and that adequate selenium
nutritional status may help protect against some of the neurological
effects of iodine deficiency [6,7].
Researchers involved in the Supplementation en Vitamines et Mineraux
AntioXydants (SU.VI.MAX) study in France, which was designed to
assess the effect of vitamin and mineral supplements on chronic
disease risk, evaluated the relationship between goiter and selenium
in a subset of this research population. Their findings suggest that
selenium supplements may be protective against goiter, which refers
to enlargement of the thyroid gland [29].
As noted above, selenium supplementation during TPN
administration is now routine [21,22].
While specific medical problems such as those described above
indicate a need for selenium supplementation, evidence is lacking
for recommending selenium supplements for healthy children and
adults.
Selenium supplements Selenium occurs in
staple foods such as corn, wheat, and soybean as selenomethionine,
the organic selenium analogue of the amino acid methionine [30,31].
Selenomethionine can be incorporated into body proteins in place of
methionine, and serves as a vehicle for selenium storage in organs
and tissues. Selenium supplements may also contain sodium selenite
and sodium selenate, two inorganic forms of selenium.
Selenomethionine is generally considered to be the best absorbed and
utilized form of selenium.
Selenium is also available in
'high selenium yeasts', which may contain as much as 1,000 to 2,000
micrograms of selenium per gram [30].
Most of the selenium in these yeasts is in the form of
selenomethionine. This form of selenium was used in the large scale
cancer prevention trial in 1983, which demonstrated that taking a
daily supplement containing 200 micrograms of selenium per day could
lower the risk of developing prostate, lung, and colorectal cancer
[32].
However, some yeasts may contain inorganic forms of selenium, which
are not utilized as well as selenomethionine.
A study
conducted in 1995 suggested that the organic forms of selenium
increased blood selenium concentration to a greater extent than
inorganic forms. However, it did not significantly improve the
activity of the selenium-dependent enzyme, glutathione peroxidase
[33].
Researchers are continuing to examine the effects of different
chemical forms of selenium, but the organic form currently appears
to be the best choice.
What are some current issues and controversies about
selenium?Selenium and cancer Observational
studies indicate that death from cancer, including lung, colorectal,
and prostate cancers, is lower among people with higher blood levels
or intake of selenium [34-40].
In addition, the incidence of nonmelanoma skin cancer is
significantly higher in areas of the United States with low soil
selenium content [37].
The effect of selenium supplementation on the recurrence of
different types of skin cancers was studied in seven dermatology
clinics in the U.S. from 1983 through the early 1990s. Taking a
daily supplement containing 200 μg of selenium did not affect
recurrence of skin cancer, but significantly reduced the occurrence
and death from total cancers. The incidence of prostate cancer,
colorectal cancer, and lung cancer was notably lower in the group
given selenium supplements [41].
Research suggests that selenium affects cancer risk in two
ways. As an anti-oxidant, selenium can help protect the body from
damaging effects of free radicals. Selenium may also prevent or slow
tumor growth. Certain breakdown products of selenium are believed to
prevent tumor growth by enhancing immune cell activity and
suppressing development of blood vessels to the tumor [42].
However,
not all studies have shown a relationship between selenium status
and cancer. In 1982, over 60,000 participants of the Nurse's Health
Study with no history of cancer submitted toenail clippings for
selenium analysis. Toenails are thought to reflect selenium status
over the previous year. After three and a half years of data
collection, researchers compared toenail selenium levels of nurses
with and without cancer. Those nurses with higher levels of selenium
in their toenails did not have a reduced risk of cancer [43].
Two important long-term studies, the SU.VI.MAX study in
France and the Selenium and Vitamin E Cancer Prevention Trial
(SELECT) study in the U.S., are now underway to further investigate
the selenium/cancer prevention link.
The SU.VI.MAX Study is
a prevention trial looking at the effects of antioxidant vitamins
and minerals on chronic diseases such as cancer and cardiovascular
disease. Doses of the nutrients provided in the study are one to
three times higher than recommended intakes, including a daily
supplement of 100 μg selenium. The SU.VI.MAX study, which began in
1994, has followed more than 12,000 adult men and women. This study
was designed to continue for eight years, and the research community
is eagerly awaiting the results of this study [44].
The SELECT study, a long-term study sponsored by the NIH, is
investigating whether supplemental selenium and/or vitamin E can
decrease the risk of prostate cancer in healthy men. Past evidence
as well as pre-clinical trials for the SELECT study suggests that
these two nutrients may be effective in preventing prostate cancer.
A daily supplement containing 200 μg of selenium will be given to
individuals in the selenium-only study group, while men in the
combined-nutrients group will receive a daily supplement containing
200 μg selenium and 400 mg vitamin E. The study, which will span
from 2001 to 2013, will include 32,400 healthy adult men [45].
Selenium and heart disease Some population
surveys have suggested an association between lower antioxidant
intake and a greater incidence of heart disease [46].
Evidence also suggests that oxidative stress from free radicals,
which are natural by-products of oxygen metabolism, may promote
heart disease [47-49].
For example, it is the oxidized form of low-density lipoproteins
(LDL, often called "bad" cholesterol) that promotes plaque build-up
in coronary arteries [48].
Selenium is one of a group of antioxidants that may help limit the
oxidation of LDL cholesterol and thereby help to prevent coronary
artery disease [47-49].
Currently there is insufficient evidence available to recommend
selenium supplements for the prevention of coronary heart disease;
however, the SU.VI.MAX study mentioned earlier is looking at the
effects of antioxidant nutrients such as selenium on heart disease.
Selenium and arthritis Surveys indicate that
individuals with rheumatoid arthritis, a chronic disease that causes
pain, stiffness, swelling, and loss of function in joints, have
reduced selenium levels in their blood [50-51].
In addition, some individuals with arthritis have a low selenium
intake [52].
The body's immune system naturally makes free radicals that
can help destroy invading organisms and damaged tissue, but that can
also harm healthy tissue [53].
Selenium, as an antioxidant, may help to relieve symptoms of
arthritis by controlling levels of free radicals [54].
Current findings are considered preliminary, and further research is
needed before selenium supplements can be recommended for
individuals with arthritis.
Selenium and
HIV HIV/AIDS malabsorption can deplete levels of many
nutrients, including selenium. Selenium deficiency is associated
with decreased immune cell counts, increased disease progression,
and high risk of death in the HIV/AIDS population [55,56].
HIV/AIDS gradually destroys the immune system, and oxidative stress
may contribute to further damage of immune cells. Antioxidant
nutrients such as selenium help protect cells from oxidative stress,
thus potentially slowing progression of the disease [57].
Selenium also may be needed for the replication of the HIV virus,
which could further deplete levels of selenium [58].
An examination of 125 HIV-positive men and women linked
selenium deficiency with a higher rate of death from HIV [59].
In a small study of 24 children with HIV who were observed for five
years, those with low selenium levels died at a younger age, which
may indicate faster disease progression [60].
Results of research studies have led experts to suggest that
selenium status may be a significant predictor of survival for those
infected with HIV [61].
Researchers continue to investigate the relationship between
selenium and HIV/AIDS, including the effect of selenium levels on
disease progression and mortality. There is insufficient evidence to
routinely recommend selenium supplements for individuals with
HIV/AIDS, but physicians may prescribe such supplements as part of
an overall treatment plan. It is also important for HIV-positive
individuals to consume recommended amounts of selenium in their
diet.
What is the health risk of too much selenium?High blood
levels of selenium (greater than 100 μg/dL) can result in a
condition called selenosis [62].
Symptoms of selenosis include gastrointestinal upsets, hair loss,
white blotchy nails, garlic breath odor, fatigue, irritability, and
mild nerve damage [2].
Selenium toxicity is rare in the U.S. The few reported cases
have been associated with industrial accidents and a manufacturing
error that led to an excessively high dose of selenium in a
supplement [63,64].
The Institute of Medicine of the National Academy of Sciences has
set a tolerable upper intake level (UL) for selenium at 400
micrograms per day for adults to prevent the risk of developing
selenosis [12].
Table 4 lists ULs for selenium, in micrograms per day, for infants,
children, and adults.
Table 4: Tolerable Upper Intake
Levels for selenium for infants, children, and adults [12]
| Age |
Males and Females (μg/day) |
| 0 - 6 months |
45 |
| 7 - 12 months |
60 |
| 1-3 y |
90 |
| 4-8 y |
150 |
| 9-13 y |
280 |
| 14-18 y |
400 |
| 19 y + |
400 |
Selecting a healthful dietThe 2000 Dietary
Guidelines for Americans states, "Different foods contain
different nutrients and other healthful substances. No single food
can supply all the nutrients in the amounts you need" [65].
For more information about building a healthful diet, refer to the
Dietary Guidelines for Americans [65] http://www.usda.gov/cnpp/DietGd.pdf
and the Food Guide Pyramid [66] http://www.nal.usda.gov/fnic/Fpyr/pyramid.html.
| |
 |



Posted Date: 12/5/2003 |
Updated: 8/1/2004 3:34:00
PM | | |
- Thomson
CD. Assessment of requirements for selenium and adequacy of
selenium status: a review. Eur J Clin Nutr 2004;58:391-402.
- Goldhaber SB. Trace element risk assessment:
essentiality vs. toxicity. Regulatory Toxicology and Pharmacology.
2003;38:232-42.
- Combs
GF, Jr and Gray WP. Chemopreventive agents: Selenium. Pharmacol
Ther 1998; 79:179-92.
- McKenzie
RC, Rafferty TS, Beckett GJ. Selenium: an essential element for
immune function. Immunol Today 1998;19:342-5.
- Levander
OA. Nutrition and newly emerging viral diseases: An overview. J
Nutr 1997;127: 948S-50S.
- Arthur
JR. The role of selenium in thyroid hormone metabolism. Can J
Physiol Pharmacol 1991;69:1648-52.
- Corvilain B, Contempre B, Longombe AO, Goyens P,
Gervy-Decoster C, Lamy F, Vanderpas JB, Dumont JE. Selenium and
the thyroid: How the relationship was established. Am J Clin Nutr
1993;57 (2 Suppl):244S-8S.
- Longnecker MP, Taylor PR, Levander OA, Howe M,
Veillon C, McAdam PA, Patterson KY, Holden JM, Stampfer MJ, Morris
JS, Willett WC. Selenium in diet, blood, and toenails in relation
to human health in a seleniferous area. Am J Clin Nutr
1991;53:1288-94.
- Pennington JA and Schoen SA. Contributions of food
groups to estimated intakes of nutritional elements: Results from
the FDA total diet studies, 1982-91. Int J Vitam Nutr Res
1996;66:342-9.
- Pennington JA and Young BE. Total diet study
nutritional elements. J Am Diet Assoc 1991;91:179-83.
- U.S.
Department of Agriculture, Agricultural Research Service. 2003.
USDA National Nutrient Database for Standard Reference, Release
16. Nutrient Data Laboratory Home Page, http://www.nal.usda.gov/fnic/foodcomp.
- Institute of Medicine, Food and Nutrition Board.
Dietary Reference Intakes: Vitamin C, Vitamin E, Selenium, and
Carotenoids. National Academy Press, Washington, DC, 2000.
- Bialostosky K, Wright JD, Kennedy-Stephenson J,
McDowell M, Johnson CL. Dietary intake of macronutrients,
micronutrients and other dietary constituents: United States
1988-94. Vital Heath Stat. 11(245) ed: National Center for Health
Statistics, 2002.
- Zhou
BF, Stamler J, Dennis B, Moag-Stahlberg A, Okuda N, Robertson C,
Zhao L, Chan Q, Elliott P for the INTERMAP Research Group.
Nutrient intakes of middle-aged men and women in China, Japan,
United Kingdom, and United States in the alte 1990s: The INTERMAP
Study. J of Human Hypertension. 2003;17:623-30.
- Ellis
DR and Salt DE. Plants, selenium and human health. Curr Opin Plant
Biol 2003;6:273-9.
- Combs
GF. Food system-based approaches to improving micronutrient
nutrition: the case for selenium. Biofactors 2000;12:39-43.
- Zimmerman MB and Kohrle J. The impact of iron and
selenium deficiencies on iodine and thyroid metabolism:
biochemistry and relevance to public health. Thyroid
2002;12:867-78.
- Beck
MA, Levander O, Handy J. Selenium deficiency and viral infection.
J of Nutr 2003;133:1463S-67S.
- Levander OA and Beck MA. Interacting nutritional and
infectious etiologies of Keshan disease. Insights from coxsackie
virus B-induced myocarditis in mice deficient in selenium or
vitamin E. Biol Trace Elem Res 1997;56:5-21.
- Levander OA. Scientific rationale for the 1989
recommended dietary allowance for selenium. J Am Diet Assoc
1991;91:1572-6.
- Gramm
HJ, Kopf A, Bratter P. The necessity of selenium substitution in
total parenteral nutrition and artificial alimentation. J Trace
Elem Med Biol 1995;9:1-12.
- Abrams
CK, Siram SM, Galsim C, Johnson-Hamilton H, Munford FL, Mezghebe
H. Selenium deficiency in long-term total parenteral nutrition.
Nutr Clin Pract 1992;7:175-8.
- Rannem
T, Ladefoged K, Hylander E, Hegnhoj J, Staun M. Selenium depletion
in patients with gastrointestinal diseases: Are there any
predictive factors? Scand J Gastroenterol 1998;33:1057-61.
- Kuroki
F, Matsumoto T, Lida M. Selenium is depleted in Crohn's disease on
enteral nutrition. Digestive Diseases 2003;21:266-70.
- Rannem
T, Ladefoged K, Hylander E, Hegnhoj J, Jarnum S. Selenium status
in patients with Crohn's disease. Am J Clin Nutr 1992;56:933-7.
- Bjerre
B, von Schenck H, Sorbo B. Hyposelaemia: Patients with
gastrointestinal diseases are at risk. J Intern Med 1989;225:85-8.
- Gartner
R, Albrich W, Angstwurm MW. The effect of a selenium
supplementation on the outcome of patients with severe systemic
inflammation, burn, and trauma. BioFactors 14 2001; 199-204.
- Berdanier, CD. Advanced Nutrition: Micronutrients.
CRC Press 1998; 208-11.
- Derumeaux H, Valeix P, Castetbon K, Bensimon M,
Boutron-Ruault MC, Arnaud J, Hercberg S. Association of selenium
with thyroid volume and echostructure in 35- to 60-year-old French
adults. Eur J Endocrinol 2003;148(3):309-15.
- Schrauzer GN. Commentary: Nutrition selenium
supplements: Product types, quality, and safety. J Am College of
Nutr 2001;20:1-4.
- Schrauzer GN. The nutritional significance,
metabolism and toxicology of selenomethionine. Adv Food Nutr Res
2003:47:73-112.
- Clark
LC, Combs Jr GF, Turnbull BW, Slate EH, Chalker D, Chow J, Davis
LS, Glover RA, Graham GF, Gross EG, Krongrad A, Lesher JL, Park
HK, Sanders BB, Smith CL, Taylor JR. Effects of selenium
supplementation for cancer prevention in patients with carcinoma
of the skin. A randomized controlled trial. J Am Med Assoc
1996;276:1957-63.
- Neve J.
Human selenium supplementation as assessed by changes in blood
selenium concentration and glutathione peroxidase activity. J
Trace Elem Med Biol 1995;9:65-73.
- Russo
MW, Murray SC, Wurzelmann JI, Woosley JT, Sandler RS. Plasma
selenium levels and the risk of colorectal adenomas. Nutr Cancer
1997;28:125-9.
- Patterson BH and Levander OA. Naturally occurring
selenium compounds in cancer chemoprevention trials: A workshop
summary. Cancer Epidemiol Biomarkers Prev 1997;6:63-9.
- Knekt
P, Marniemi J, Teppo L, Heliovaara M, Aromaa A. Is low selenium
status a risk factor for lung cancer? Am J Epidemiol
1998;148:975-82.
- Fleet
JC. Dietary selenium repletion may reduce cancer incidence in
people at high risk who live in areas with low soil selenium. Nutr
Rev 1997;55:277-9.
- Shamberger RJ. The genotoxicity of selenium. Mutat
Res 1985;154:29-48.
- Young
KL and Lee PN. Intervention studies on cancer. Eur J Cancer Prev
1999;8:91-103.
- Burguera JL, Burguera M, Gallignani M, Alarcon OM,
Burgueera JA. Blood serum selenium in the province of Merida,
Venezuela, related to sex, cancer incidence and soil selenium
content. J Trace Elem Electrolytes Health Dis 1990;4:73-7.
- Combs
GF, Jr., Clark LC, Turnbull BW. Reduction of cancer risk with an
oral supplement of selenium. Biomed Environ Sci 1997;10:227-34.
- Combs
GF, Clark LC, Turnbull BW. An analysis of cancer prevention by
selenium. BioFactors 14 2001; 153-9.
- Garland
M, Morris JS, Stampfer MJ, Colditz GA, Spate VL, Baskett CK,
Rosner B, Speier FE, Willett WC, Hunter DJ. Prospective study of
toenail selenium levels and cancer among women. J Natl Cancer Inst
1995;87:497- 505.
- Hercberg S, Galan P, Preziosi P, Roussel AM, Arnaud
J, Richard MJ, Malvy D, Paul-Dauphin A, Briancon S, Favier A.
Background and rationale behind the SU.VI.MAX Study, a prevention
trial using nutritional doses of a combination of antioxidant
vitamins and minerals to reduce cardiovascular diseases and
cancers. Supplementation en VItamines et Mineraux AntiXydants
Study. Int J Vitam Nutr Res 1998;68:3-20.
- Klein
EA, Thompson IM, Lippman SM, Goodman PJ, Albanes D, Taylor PR,
Coltman C. SELECT: the next prostate cancer prevention trial.
Selenium and Vitamin E Cancer Prevention Trial. Journal of Urology
2001;166(4):1311-5.
- Gey KF.
Vitamins E plus C and interacting conutrients required for optimal
health. A critical and constructive review of epidemiology and
supplementation data regarding cardiovascular disease and cancer.
Biofactors 1998;7:113-74.
- Ozer
NK, Boscoboinik D, Azzi A. New roles of low density lipoproteins
and vitamin E in the pathogenesis of atherosclerosis. Biochem Mol
Biol Int 1995;35:117-24.
- Lapenna
D, de Gioia S, Ciofani G, Mezzetti A, Ucchino S, Calafiore AM,
Napolitano AM, Di Ilio C, Cuccurulo F. Glutathione-related
antioxidant defenses in human atherosclerotic plaques. Circulation
1998;97:1930-4.
- Neve J.
Selenium as a risk factor for cardiovascular diseases. J
Cardiovasc Risk 1996;3:42-7.
- Kose K,
Dogan P, Kardas Y, Saraymen R. Plasma selenium levels in
rheumatoid arthritis. Biol Trace Elem Res 1996;53:51-6.
- Heliovaara M, Knekt P, Aho K, Aaran RK, Alfthan G,
Aromaa A. Serum antioxidants and risk of rheumatoid arthritis. Ann
Rheum Dis 1994;53:51-3.
- Stone
J, Doube A, Dudson D, Wallace J. Inadequate calcium, folic acid,
vitamin E, zinc, and selenium intake in rheumatoid arthritis
patients: Results of a dietary survey. Semin Arthritis Rheum
1997;27:180-5.
- Grimble
RF. Nutritional antioxidants and the modulation of inflammation:
Theory and practice. New Horizons 1994;2:175-85.
- Aaseth
J, Haugen M, Forre O. Rheumatoid arthritis and metal compounds-
perspectives on the role of oxygen radical detoxification. Analyst
1998;123:3- 6.
- Look
MP, Rockstroh JK, Rao GS, Kreuzer KA, Spengler U, Sauerbruch T.
Serum selenium versus lymphocyte subsets and markers of disease
progression and inflammatory response in human immunodeficiency
virus-1 infection. Biol Trace Elem Res 1997;56(1):31-41.
- Singhal
N and Austin J. A clinical review of micronutrients in HIV
infection. J Int Assoc Physicians AIDS Care 2002;1:63-75.
- Romero-Alvira D and Roche E. The keys of oxidative
stress in acquired immune deficiency syndrome apoptosis. Medical
Hypotheses 1998;51(2):169-73.
- Patrick
L. Nutrients and HIV; Part One - Beta carotene and selenium.
Altern Med Rev 1999;4:403-13.
- Baum
MK, Shor-Posner G, Lai S, Zhang G, Lai H, Fletcher MA, Sauberlich
H, Page JB. High risk of HIV-related mortality is associated with
selenium deficiency. J Acquir Immune Defic Syndr Hum Retrovirol
1997;15:370-4.
- Campa
A, Shor-Posner G, Indacoche F, Zhang G, Lai H, Asthana D, Scott
GB, Baum MK. Mortality risk in selenium-deficient HIV-positive
children. J Acquir Immune Defic Syndr Hum Retrovirol
1999;15:508-13.
- Baum MK
and Shor-Posner G. Micronutrient status in relationship to
mortality in HIV-1 disease. Nutr Rev 1998;56:S135-9.
- Koller
LD and Exon JH. The two faces of selenium-deficiency and toxicity
are similar in animals and man. Can J Vet Res 1986;50:297-306.
- Hathcock J. Vitamins and minerals: Efficacy and
safety. Am J Clin Nutr 1997;66:427-37.
- Raisbeck MF, Dahl ER, Sanchez DA, Belden EL, O'Toole
D. Naturally occurring selenosis in Wyoming. J Vet Diagn Invest
1993;5:84-7.
- Dietary
Guidelines Advisory Committee, Agricultural Research Service,
United States Department of Agriculture (USDA). HG Bulletin No.
232, 2000. http://www.usda.gov/cnpp/DietGd.pdf.
- Center
for Nutrition Policy and Promotion, United Stated Department of
Agriculture. Food Guide Pyramid, 1992 (slightly revised 1996). http://www.nal.usda.gov/fnic/Fpyr/pyramid.html.
|
 Reasonable care has been taken in preparing
this document and the information provided herein is believed to be
accurate. However, this information is not intended to constitute an
"authoritative statement" under Food and Drug Administration rules
and regulations. |
 The mission of the Office of Dietary
Supplements (ODS) is to strengthen knowledge and understanding of
dietary supplements by evaluating scientific information,
stimulating and supporting research, disseminating research results,
and educating the public to foster an enhanced quality of life and
health for the U.S. population.
The Warren Grant Magnuson
Clinical Center is the clinical research hospital for NIH. Through
clinical research, physicians and scientist translate laboratory
discoveries into better treatments, therpaies and interventions to
improve the nation's health. |

Health professionals and consumers need credible information to
make thoughtful decisions about eating a healthful diet and using
vitamin and mineral supplements. To help guide those decisions,
registered dietitians at the Warren Grant Magnuson Clinical Center,
the clinical research hospital at the National Institutes of Health
(NIH) in Bethesda, MD, developed a series of Fact Sheets in
conjunction with the Office of Dietary Supplements in the Office of
the Director of NIH. These fact sheets provide responsible
information about the role of vitamins and minerals in health and
disease. Each Fact Sheet in this series received extensive review by
recognized experts from the academic and research communities.
The information is not intended to be a substitute for
professional medical advice. It is important to seek the advice of a
physician about any medical condition or symptom. It is also
important to seek the advice of a physician, registered dietitian,
pharmacist, or other qualified health professional about the
appropriateness of taking dietary supplements and their potential
interactions with medications. |
 The Clinical Nutrition Service and the ODS
thank the expert scientific reviewers for their role in ensuring the
scientific accuracy of the information discussed in these fact
sheets, along with the Nutrition Education Subcommittee of the NIH,
the U.S. Department of Agriculture Dietary Guidance Working Group,
and the Department of Health and Human Services Nutrition Policy
Board Committee on Dietary Guidance. Reviewers:
Jed Fahey,
M.S., Johns Hopkins School of Medicine
Marianna Fordyce-Baum,
Ph.D., University of Miami School of Medicine
Orville
Levander, Ph.D., USDA, Agricultural Research Service, Beltsville,
Maryland
Keith West, Dr.P.H., Johns Hopkins University School
of Science and Public Health
Sedigheh Yamini, Ph.D., USDA,
Center for Nutrition Policy and Promotion
| |