When the Dietary Supplement Health and Education Act (DSHEA) was passed in 1994, it allowed dietary supplements such as vitamins, herb and botanicals, minerals, amino acids, tissue extract (i.e., tissues or enzymes from organs or glands), and metabolites, concentrates, constituents or extracts to be regulated as a food product rather than a pharmaceutical.1 As a result, dietary supplements do not need to be proven effective nor safe while at the same time they cannot make claims to cure, treat, nor prevent disease. It is under the guise of the DSHEA that enable potent chemicals like the hormone dehydroepiandrosterone (DHEA) to be marketed as a dietary supplement allowing it to bypass having to prove efficacy.
DHEA is naturally produced by the adrenal glands and is the precursor to androstendione (commonly known as “andro” in the body building world) and androstendiol which further produce testosterone and the estrogens estrone and estradiol.2 While DHEA cannot be labeled nor marketed to make claims to increase strength, increase endurance, enhance energy, or increase muscle mass, all it takes is one “news article” in a muscle or health magazine to mention DHEA can be used for these enhancements. Everyone is looking for the easy solution to improved sport performance or physical appearance. In addition to these ergogenic claims, DHEA has been promoted as being effective for strengthening the immune system, enhancing libido, preventing cancer and cardiovascular disease and as an anti-aging agent.3
Since DHEA is the precursor to androstenedione and androstenediol, many athletes take supplemental DHEA to increase testosterone and therefore muscle mass. However, studies have shown that there is conflicting evidence that any such effects could be elicited by oral DHEA therapy.4,5 There is some concern however that it can produce androgen qualities in women.6
When taken orally, DHEA is unlikely to have much effect on muscle-building enhancement or sports performance. According to Baechle, et.al., when taken orally only a small portion of DHEA can be converted to testosterone.7 In human metabolic pathways, DHEA can also be converted to estrogens as well as the androgens. DHEA has only one tenth the biological activity of testosterone.8
What about the side effects? No long term studies have been performed to determine effectiveness or safety. In a study of 50 women, supplemental DHEA of 50-200mg increased serum DHEA as well as serum testosterone. Over 50% of these women experienced acne, 18% increased facial hair, and 8% had increased perspiration. Less common side effects included breast tenderness, weight gain, mood alteration, headache, oily skin and irregular menstruation.9
Two studies10,11 have shown remarkable increases in serum testosterone in both men and women. However, others as reported above and another as reported in the Journal of Endocrinology12 report testosterone increases in women only. There are concerns that some people have the ability to utilize DHEA for making testosterone better than others. This could explain the inconsistency but obviously further study is warranted.
Increases in testosterone may increase ones risk of certain cancers. It is our clinical experience that supplemental DHEA can increase PSA levels in men. It has been documented that high amounts of DHEA can also cause liver cancer in animals.13,14 Some doctors prescribe DHEA for those with adrenal insufficiency, impotence, and osteoporosis.16 Because of the potential for cancer, doctors recommend that those who take DHEA should have their liver enzymes tested regularly. In a six month trial, supplementation with DHEA increased insulin-like growth factor levels at 3 months and decreased high-density lipoprotein (HDL) and apolipoprotein A1 levels at 6 months.15 Increasing IGF might increase the risk of breast cancer whereas decreasing HDL could increase the risk for heart disease.
In conclusion, there are too many conflicting studies to determine the efficacy of DHEA and there is definitely enough evidence to have conerns for it’s safety. Because high doses can inhibit ones own ability to make DHEA16, one must first determine need for DHEA via blood analysis but this doesn’t really answer the question as to “why” there may be low levels of DHEA in an individual. Hormonal imbalances are only an indication of some underlying metabolic imbalance that is occurring. Get tested properly, supplementing based upon your test results and cleaning up lifestyle habits is the best way to balance hormones.
REFERENCES:
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Center for Food Safety & Applied Nutrition [Food and Drug Administration Web site]. Dietary supplements. Accessed at: http://www.cfsan.fda.gov/~dms/ds-oview.html#what , June 7, 2008.
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Figure 1. Biosynthesis of Testosterone and Related Compounds
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Ambrose, Peter, Drug Use in Sports: A Veritable Arena for Pharmacists. Dietary Supplements Used in Sports. J Am Pharm Assoc 44(4):501-516, 2004. Medscape Today: accessed June 7, 2008
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Brown GA, Vukovich MD, Martini ER, et al. Effects of androstenedione-herbal supplementation on serum sex hormone concentrations in 30- to 59-year-old men. Int J Vitam Nutr Res. 2001;71:293-301.
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Wallace MB, Lim J, Cutler A, Bucci L. Effects of dehydroepiandrosterone vs androstenedione supplementation in men. Med Sci Sports Exerc. 1999;31:1788-92.
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Anonymous. Dehydroepiandrosterone (DHEA). Med Lett Drugs Ther. 1996;38:91-2.
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Baechle, et.al., Essentials of Strength Training and Conditioning, 2nd Edition. Page 213
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Migeon, C.J. Adrenal androgens in man. Am.J.Med. 53:606-626. 1972
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van Vollenhoven RF, et.al.,. Treatment of systemic lupus erythematosus with dehydroepiandrosterone: 50 patients treated up to 12 months. J Rheumatol 1998;25:285–9.
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Wolf OT, Neumann O, Hellhammer DH, et al. Effects of a two-week physiological dehydroepiandrosterone substitution on cognitive performance and well-being in healthy elderly women and men. J Clin Endocrinol Metab 1997;82:2263–7.
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Bowers LD. Oral dehydroepiandrosterone supplementation can increase the testosterone/epitestosterone ratio. Clin Chem 1999;45:295–6.
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Morales AJ, Nolan JJ, Nelson JC, Yen SSC. Effects of replacement dose of DHEA in men and women of advancing age. J Clin Endocrinol Metab 1994;78:1360.
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Orner GA, Mathews C, Hendricks JD, et al. Dehydroepiandrosterone is a complete hepatocarcinogen and potent tumor promoter in the absence of peroxisome proliferation in rainbow trout. Carcinogenesis 1995;16:2893–8.
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Metzger C, Mayer D, Hoffmann H, et al. Sequential appearance and ultrastructure of amphophilic cell foci, adenomas, and carcinomas in the liver of male and female rats treated with dehydroepiandrosterone. Toxicol Pathol 1995;23:591–605.
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Casson PR, Santoro N, Elkind-Hirsch K, et al. Postmenopausal dehydroepiandrosterone administration increases free insulin-like growth factor-I and decreases high-density lipoprotein: a six-month trial. Fertil Steril 1998;70:107–10.
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University of Maryland Medical Center: DHE