Sr. Tollin et al., FINASTERIDE THERAPY DOES NOT ALTER DONE TURNOVER IN MEN WITH BENIGN PROSTATIC HYPERPLASIA - A CLINICAL RESEARCH-CENTER STUDY, The Journal of clinical endocrinology and metabolism, 81(3), 1996, pp. 1031-1034
Benign prostatic hyperplasia is often treated with finasteride, which
inhibits the conversion of testosterone to dihydrotestosterone (DHT).
Aside from the prostate, other androgen-dependent tissues seem to be u
naffected by selective DHT deficiency, but the affect on bone density
in humans has not Set been defined. To study this question, we compare
d indices of bone turnover and bone mineral density in 35 men treated
with finasteride with controls. Bone resorption was assessed by measur
ing urinary excretion of N-telopeptide cross-links of type I collagen
and hydroxyproline, and bone formation was assessed by measuring serum
osteocalcin and bonespecific alkaline phosphatase. Bone density of th
e spine and hip were assessed by dual energy x-ray absorptiometry. We
found that finasteride-treated patients had mean DHT levels 81% lower
than controls (P < 0.0001). There were no significant differences betw
een the two groups in any of the markers of bone turnover or measures
of bone density. These results suggest that testosterone can maintain
bone density in men even in the absence of DHT. Although long term stu
dies are needed, our results suggest that men who take finasteride are
not at increased risk for bone loss.