DHEA in Elderly Women and DHEA or Testosterone in Elderly Men
K. Sreekumaran Nair, M.D., Ph.D., Robert A. Rizza, M.D., Peter O'Brien, Ph.D., Ketan Dhatariya, M.D., M.R.C.P., Kevin R. Short, Ph.D., Ajay Nehra, M.D., Janet L. Vittone, M.D., George G. Klee, M.D., Ananda Basu, M.D., Rita Basu, M.D., Claudio Cobelli, Ph.D., Gianna Toffolo, Ph.D., Chiara Dalla Man, Ph.D., Donald J. Tindall, Ph.D., L. Joseph Melton, III, M.D., Ph.D., Glenn E. Smith, Ph.D., Sundeep Khosla, M.D., and Michael D. Jensen, M.D.
Background Dehydroepiandrosterone (DHEA) and testosterone arewidely promoted as antiaging supplements, but the long-termbenefits, as compared with potential harm, are unknown.
Methods We performed a 2-year, placebo-controlled, randomized,double-blind study involving 87 elderly men with low levelsof the sulfated form of DHEA and bioavailable testosterone and57 elderly women with low levels of sulfated DHEA. Among themen, 29 received DHEA, 27 received testosterone, and 31 receivedplacebo. Among the women, 27 received DHEA and 30 received placebo.Outcome measures included physical performance, body composition,bone mineral density (BMD), glucose tolerance, and quality oflife.
Results As compared with the change from baseline to 24 monthsin the placebo group, subjects who received DHEA for 2 yearshad an increase in plasma levels of sulfated DHEA by a medianof 3.4 µg per milliliter (9.2 µmol per liter) inmen and by 3.8 µg per milliliter (10.3 µmol perliter) in women. Among men who received testosterone, the levelof bioavailable testosterone increased by a median of 30.4 ngper deciliter (1.1 nmol per liter), as compared with the changein the placebo group. A separate analysis of men and women showedno significant effect of DHEA on body-composition measurements.Neither hormone altered the peak volume of oxygen consumed perminute, muscle strength, or insulin sensitivity. Men who receivedtestosterone had a slight increase in fat-free mass, and menin both treatment groups had an increase in BMD at the femoralneck. Women who received DHEA had an increase in BMD at theultradistal radius. Neither treatment improved the quality oflife or had major adverse effects.
Conclusions Neither DHEA nor low-dose testosterone replacementin elderly people has physiologically relevant beneficial effectson body composition, physical performance, insulin sensitivity,or quality of life. (ClinicalTrials.gov number, NCT00254371
[ClinicalTrials.gov]
.)
Source Information
From the Division of Endocrinology (K.S.N., R.A.R., K.D., K.R.S., A.B., R.B., S.K., M.D.J.) and the Departments of Health Sciences Research (P.O., L.J.M.), Urology (A.N., D.J.T.), Medicine (J.L.V.), Laboratory Medicine and Pathology (G.G.K.), and Psychology (G.E.S.), Mayo Clinic, Rochester, MN; and the Department of Information Engineering, University of Padua, Padua, Italy (C.C., G.T., C.D.M.). Drs. Khosla and Jensen contributed equally to this article.
Address reprint requests to Dr. Nair at the Division of Endocrinology, Mayo Clinic, 200 First St. SW, 5-194 Joseph, Rochester, MN 55905, or at nair.sree{at}mayo.edu.
DHEA and Testosterone in the Elderly
Page S. T., Matsumoto A. M., Bremner W. J., Yasuda M., Horie S., Perls T. T., Gleicher N., Barad D., Nair K. S., Smith G.
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N Engl J Med 2007;
356:635-637, Feb 8, 2007.
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