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5α-还原酶抑制剂非那雄胺治疗特发性多毛症的临床及激素效应

Clinical and hormonal effects of the 5 alpha-reductase inhibitor finasteride in idiopathic hirsutism.

作者信息

Moghetti P, Castello R, Magnani C M, Tosi F, Negri C, Armanini D, Bellotti G, Muggeo M

机构信息

Division of Metabolic Diseases, University of Verona, Italy.

出版信息

J Clin Endocrinol Metab. 1994 Oct;79(4):1115-21. doi: 10.1210/jcem.79.4.7962284.

DOI:10.1210/jcem.79.4.7962284
PMID:7962284
Abstract

Hyperactivity of 5 alpha-reductase in the skin is considered a major mechanism of excessive hair growth in hirsute women with normal levels of serum androgens (idiopathic hirsutism). Preventing the conversion of testosterone to dihydrotestosterone by inhibiting 5 alpha-reductase activity could thus be the most rational and effective treatment in this condition. The present study evaluated the effects of the oral administration of finasteride (5 mg once daily) for 6 months in 17 young women with idiopathic hirsutism, 5 of whom were also given an oral contraceptive. The degree of hirsutism (graded by a modified Ferriman-Gallwey score), serum sex hormone levels, and serum and urinary 5 alpha-metabolism steroid profiles were determined basally and periodically during the treatment period. The modified Ferriman-Gallwey score showed a remarkable reduction after 6 months of finasteride treatment (5.9 +/- 0.6 vs. 11.7 +/- 1.3; P < 0.01). Serum 5 alpha-dihydrotestosterone and 3 alpha-androstanediol glucuronide levels were decreased, and urinary C19 and C21 5 beta/5 alpha metabolite ratios were increased compared with pretreatment values. No significant adverse effect was reported. In women treated with finasteride and oral contraceptive, clinical efficacy was slightly more pronounced. In conclusion, the 5 alpha-reductase inhibitor finasteride is well tolerated and seems to be a useful tool in the treatment of idiopathic hirsutism.

摘要

皮肤中5α-还原酶活性亢进被认为是血清雄激素水平正常的多毛女性(特发性多毛症)毛发过度生长的主要机制。因此,通过抑制5α-还原酶活性来阻止睾酮转化为二氢睾酮可能是这种情况下最合理、有效的治疗方法。本研究评估了17名患有特发性多毛症的年轻女性口服非那雄胺(每日1次,每次5mg)6个月的效果,其中5名女性还同时服用了口服避孕药。在治疗期间,定期测定多毛症程度(采用改良的Ferriman-Gallwey评分法分级)、血清性激素水平以及血清和尿液中5α-代谢类固醇谱。非那雄胺治疗6个月后,改良的Ferriman-Gallwey评分显著降低(5.9±0.6对11.7±1.3;P<0.01)。与治疗前相比,血清5α-二氢睾酮和3α-雄烷二醇葡糖苷酸水平降低,尿液中C19和C21 5β/5α代谢物比值升高。未报告明显不良反应。在同时接受非那雄胺和口服避孕药治疗的女性中,临床疗效略为显著。总之,5α-还原酶抑制剂非那雄胺耐受性良好,似乎是治疗特发性多毛症的有效药物。

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