Exogenous testosterone or testosterone with finasteride increases bone mineral density in older men with low serum testosterone
| dc.contributor.author | Sutton, Paul R. | en_US |
| dc.contributor.author | Bremner, William J. | en_US |
| dc.contributor.author | Easley, Kirk A. | en_US |
| dc.contributor.author | Tenover, J. Lisa | en_US |
| dc.contributor.author | Matsumoto, Alvin M. | en_US |
| dc.contributor.author | Anawalt, Bradley D. | en_US |
| dc.contributor.author | Amory, John K. | en_US |
| dc.contributor.author | Watts, Nelson B. | en_US |
| dc.date.accessioned | 2008-10-17T20:41:41Z | |
| dc.date.available | 2008-10-17T20:41:41Z | |
| dc.date.issued | 2004-02 | en_US |
| dc.description.abstract | Older men, particularly those with low serum testosterone (T) levels, might benefit from T therapy to improve bone mineral density (BMD) and reduce fracture risk. Concerns exist, however, about the impact of T therapy on the prostate in older men. We hypothesized that the combination of T and finasteride (F), a 5 alpha-reductase inhibitor, might increase BMD in older men without adverse effects on the prostate. Seventy men aged 65 yr or older, with a serum T less than 12.1 nmol/liter on two occasions, were randomly assigned to receive one of three regimens for 36 months: T enanthate, 200 mg im every 2 wk with placebo pills daily (T-only); T enanthate, 200 mg every 2 wk with 5 mg F daily (T+F); or placebo injections and pills (placebo). Low BMD was not an inclusion criterion. We obtained serial measurements of BMD of the lumbar spine and hip by dual x-ray absorptiometry. Prostate-specific antigen (PSA) and prostate size were measured at baseline and during treatment to assess the impact of therapy on the prostate. Fifty men completed the 36-month protocol. By an intent-to-treat analysis including all men for as long as they contributed data, T therapy for 36 months increased BMD in these men at the lumbar spine [10.2 +/- 1.4% (mean percentage increase from baseline +/- SEM; T-only) and 9.3 +/- 1.4% (T+F) vs. 1.3 +/- 1.4% for placebo (P < 0.001)] and in the hip [2.7 +/- 0.7% (T-only) and 2.2 +/- 0.7% (T+F) vs. -0.2 +/- 0.7% for placebo, (P < or = 0.02)]. Significant increases in BMD were seen also in the intertrochanteric and trochanteric regions of the hip. After 6 months of therapy, urinary deoxypyridinoline (a bone-resorption marker) decreased significantly compared with baseline in both the T-only and T+F groups (P < 0.001) but was not significantly reduced compared with the placebo group. Over 36 months, PSA increased significantly from baseline in the T-only group (P < 0.001). Prostate volume increased in all groups during the 36-month treatment period, but this increase was significantly less in the T+F group compared with both the T-only and placebo groups (P = 0.02). These results demonstrate that T therapy in older men with low serum T increases vertebral and hip BMD over 36 months, both when administered alone and when combined with F. This finding suggests that dihydrotestosterone is not essential for the beneficial effects of T on BMD in men. In addition, the concomitant administration of F with T appears to attenuate the impact of T therapy on prostate size and PSA and might reduce the chance of benign prostatic hypertrophy or other prostate-related complications in older men on T therapy. These findings have important implications for the prevention and treatment of osteoporosis in older men with low T levels. | en_US |
| dc.identifier.citation | J Clin Endocrinol Metab. 2004 Feb;89(2):503-10 | en_US |
| dc.identifier.uri | http://hdl.handle.net/1773/4369 | |
| dc.language.iso | en_US | en_US |
| dc.publisher | Endocrine Society | en_US |
| dc.subject | colchicine | en_US |
| dc.subject | male contraception | en_US |
| dc.subject | testosterone | en_US |
| dc.subject | andrology | en_US |
| dc.subject | reifenstein's syndrome | en_US |
| dc.subject | spermatogenesis | en_US |
| dc.subject | klinefelter's syndrome | en_US |
| dc.subject | 5-alpha reductase inhibitors | en_US |
| dc.subject | gonadotropins | en_US |
| dc.subject.mesh | Aged | en_US |
| dc.subject.mesh | Drug Therapy, Combination | en_US |
| dc.subject.mesh | Finasteride, therapeutic use | en_US |
| dc.subject.mesh | Bone Density, drug effects | en_US |
| dc.subject.mesh | Prostate, drug effects, pathology | en_US |
| dc.subject.mesh | Humans | en_US |
| dc.subject.mesh | Male | en_US |
| dc.subject.mesh | Research Support, U.S. Gov't, P.H.S. | en_US |
| dc.subject.mesh | Enzyme Inhibitors, therapeutic use | en_US |
| dc.subject.mesh | Organ Size, drug effects | en_US |
| dc.subject.mesh | Testosterone, adverse effects, analogs & derivatives, blood, therapeutic use | en_US |
| dc.subject.mesh | Prostate-Specific Antigen, blood | en_US |
| dc.title | Exogenous testosterone or testosterone with finasteride increases bone mineral density in older men with low serum testosterone | en_US |
| dc.type | Article | en_US |
