Hypervitaminosis

Vitamin overdose
Classification and external resources
ICD-10 E67.0-E67.3
ICD-9 278.2, 278.4
Patient UK Hypervitaminosis

Hypervitaminosis refers to a condition of abnormally high storage levels of vitamins, which can lead to toxic symptoms. The medical names of the different conditions are derived from the vitamin involved: an excess of vitamin A, for example, is called hypervitaminosis A.

Generally, toxic levels of vitamins stem from high supplement intake and not from dietary sources. Toxicities of fat-soluble vitamins can also be caused by a large intake of highly fortified foods, but foods rarely deliver dangerous levels of fat-soluble vitamins.[1]

The Dietary Reference Intake recommendations from the United States Department of Agriculture define a "tolerable upper intake level" for most vitamins.

High dosage vitamin A; high dosage, slow release vitamin B3; and very high dosage vitamin B6 alone (i.e. without vitamin B complex) are sometimes associated with vitamin side effects that usually rapidly cease with supplement reduction or cessation.

Fat soluble

With few exceptions, like some vitamins from B complex, hypervitaminosis usually occurs more with fat-soluble vitamins (D, E, K and A or 'DEKA'), which are stored in the liver and fatty tissues of the body. These vitamins build up and remain for a longer time in the body than water soluble vitamins.[1]

Conditions include:

Minerals

High doses of mineral supplements can also lead to side effects and toxicity. Mineral-supplement poisoning does occur occasionally, most often due to excessive intake of iron-containing supplements.

Comparative safety statistics

In the United States, overdose exposure to all formulations of "vitamins" was reported by 62,562 individuals in 2004 (nearly 80% [~78%, n=48,989] of these exposures were in children under the age of 6), leading to 53 "major" life-threatening outcomes and 3 deaths (2 from vitamins D and E; 1 from polyvitaminic type formula, with iron and no fluoride).[2] This may be compared to the 19,250 people who died of unintentional poisoning of all kinds in the U.S. in the same year (2004).[3] In 2010, 71,000 exposures to various vitamins and multivitamin-mineral formulations were reported to poison control centers, which resulted in 15 major reactions but no deaths.[4]

Before 1998, several deaths per year were associated with pharmaceutical iron-containing supplements, especially brightly colored, sugar-coated, high-potency iron supplements, and most deaths were children.[5] Unit packaging restrictions on supplements with more than 30 mg of iron have since reduced deaths to 0 or 1 per year.[5] These statistics compare with 59 confirmed deaths due to aspirin poisoning in 2003 [6] and 147 deaths known to be associated with acetaminophen-containing products in 2003.[6]

See also

References

  1. 1.0 1.1 Sizer, Frances Sienkiewicz; Ellie Whitney (2008). Nutrition: Concepts and Controversies (11 ed.). United States of America: Thomson Wadsworth. pp. 221, 235. ISBN 0-495-39065-8.
  2. Toxic Exposure Surveillance System (2004). "Annual Report" (pdf). American Association of Poison Control Centers.
  3. "National Center for Health Statistics".
  4. Bronstein, A. C.; Spyker, D. A.; Cantilena, L. R.; Green, J. L.; Rumack, B. H.; Dart, R. C. (2011). "2010 Annual Report of the American Association of Poison Control Centers' National Poison Data System (NPDS): 28th Annual Report". Clinical Toxicology 49 (10): 910–941. doi:10.3109/15563650.2011.635149. PMID 22165864.
  5. 5.0 5.1 Tenenbein M (2005). "Unit-dose packaging of iron supplements and reduction of iron poisoning in young children". Arch Pediatr Adolesc Med 159 (6): 557–60. doi:10.1001/archpedi.159.6.557. PMID 15939855.
  6. 6.0 6.1 Watson WA, Litovitz TL, Klein-Schwartz W et al. (2004). "2003 annual report of the American Association of Poison Control Centers Toxic Exposure Surveillance System". Am J Emerg Med 22 (5): 335–404. doi:10.1016/j.ajem.2004.06.001. PMID 15490384.