Overstreet J W, Fuh V L, Gould J, Howards S S, Lieber M M, Hellstrom W, Shapiro S, Carroll P, Corfman R S, Petrou S, Lewis R, Toth P, Shown T, Roy J, Jarow J P, Bonilla J, Jacobsen C A, Wang D Z, Kaufman K D
Department of Obstetrics and Gynecology, University of California, Davis, USA.
J Urol. 1999 Oct;162(4):1295-300.
Finasteride, an oral type 2, 5alpha-reductase inhibitor, is used in 1 mg. daily doses for the treatment of male pattern hair loss. A dose of 5 mg. finasteride daily reduces ejaculate volume by approximately 25%, and reduces prostate volume by approximately 20% and serum prostate specific antigen (PSA) by approximately 50% in men with benign prostatic hyperplasia. To our knowledge no data exist on the effect of 1 mg. finasteride daily on ejaculate volume or other semen parameters, or on the prostate in young men. Therefore, we studied the potential effect and reversibility of effect of 1 mg. finasteride daily on spermatogenesis, semen production, the prostate and serum PSA in young men.
In this double-blind, placebo controlled multicenter study 181 men 19 to 41 years old were randomized to receive 1 mg. finasteride or placebo for 48 weeks followed by a 60-week off-drug period. Of the 181 men 79 were included in a subset for the collection and analysis of sequential semen samples.
There were no significant effects of 1 mg. finasteride on sperm concentration, total sperm per ejaculate, sperm motility or morphology. Ejaculate volume in subjects on finasteride decreased 0.3 ml. (-11%) compared to a decrease of 0.2 ml. (-8%) for placebo, with a median between treatment group difference of -0.03 ml. (1%, 90% confidence interval -10.4 to 13.1, p = 0.915). There were significant but small decreases in prostate volume (-2.6%) and serum PSA (-0.2 ng./ml.) in the finasteride group, which reversed on discontinuation of the drug.
Treatment with 1 mg. finasteride daily for 48 weeks did not affect spermatogenesis or semen production in young men. The effects of 1 mg. finasteride daily on prostate volume and serum PSA in young men without benign prostatic hyperplasia were small and reversible on discontinuation of the drug.
非那雄胺是一种口服2型5α-还原酶抑制剂,每日剂量1mg用于治疗男性型脱发。每日剂量5mg非那雄胺可使良性前列腺增生男性的射精量减少约25%,前列腺体积减少约20%,血清前列腺特异性抗原(PSA)减少约50%。据我们所知,尚无关于每日1mg非那雄胺对年轻男性射精量或其他精液参数以及前列腺影响的数据。因此,我们研究了每日1mg非那雄胺对年轻男性精子发生、精液生成、前列腺和血清PSA的潜在影响及作用的可逆性。
在这项双盲、安慰剂对照的多中心研究中,181名年龄在19至41岁的男性被随机分为接受1mg非那雄胺或安慰剂治疗48周,随后为60周的停药期。181名男性中有79名被纳入一个亚组,用于采集和分析连续的精液样本。
1mg非那雄胺对精子浓度、每次射精的总精子数、精子活力或形态均无显著影响。服用非那雄胺的受试者射精量减少了0.3ml(-11%),而安慰剂组减少了0.2ml(-8%),治疗组之间的中位数差异为-0.03ml(1%,90%置信区间-10.4至13.1,p = 0.915)。非那雄胺组前列腺体积(-2.6%)和血清PSA(-0.2ng/ml)有显著但微小的下降,停药后恢复。
每日服用1mg非那雄胺48周对年轻男性的精子发生或精液生成无影响。每日1mg非那雄胺对无良性前列腺增生的年轻男性前列腺体积和血清PSA的影响较小,停药后可逆。