MA (Master of Arts)
Kinesiology and Sport Studies
Date of Award
Committee Chair or Co-Chairs
Diego de Hoyos
Diana Mozen, Kevin Breuel
Recent evidence suggests that declining bone mineral density (BMD) in males is related to declining circulating estrogens. The majority of endogenous plasma estrogens in males result from peripheral aromatization of plasma androgens. Thus, it was hypothesized that dietary supplementation with an aromatizable androgen (androstenedione) may stimulate increases in BMD.
BMD (measured by dual energy x-ray absorptiometry) and biochemical markers of bone turnover (1, 25 OH2 Vitamin D, calcitonin, deoxypyrodinoline, and parathyroid hormone) were assessed before and after 12 weeks of dietary androstenedione supplementation (200 mg/d). Twenty-four volunteers were randomized into either an androstenedione supplementation or placebo groups. Study volunteers also performed high intensity resistance training (RT) during the treatment period.
Androstenedione supplementation significantly increased plasma estradiol-17β levels by 82%. However, the increase in estradiol-17β did not impact bone turnover. The RT regimen did stimulate significant, local increases in BMD. Spine BMD was significantly increased by 6% for both treatment groups.
Thesis - Open Access
Wills, Troy Matthew, "The Osteogenic Effects of 12 Weeks of Oral Supplementation of Androstenedione in Middle-Aged Men." (2003). Electronic Theses and Dissertations. Paper 829. http://dc.etsu.edu/etd/829
Copyright by the authors.