Exogenous testosterone or testosterone with finasteride increases bone mineral density in older men with low serum testosterone
Date
2004-02Author
Sutton, Paul R.
Bremner, William J.
Easley, Kirk A.
Tenover, J. Lisa
Matsumoto, Alvin M.
Anawalt, Bradley D.
Amory, John K.
Watts, Nelson B.
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Show full item recordAbstract
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.