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5α-还原酶抑制剂非那雄胺治疗特发性多毛症的长期疗效:1年治疗期及1年随访期的临床和激素效应

Outcome of long-term treatment with the 5 alpha-reductase inhibitor finasteride in idiopathic hirsutism: clinical and hormonal effects during a 1-year course of therapy and 1-year follow-up.

作者信息

Castello R, Tosi F, Perrone F, Negri C, Muggeo M, Moghetti P

机构信息

Divisione Clinicizzata di Endocrinologia e Malattie del Metabolismo, University of Verona, Italy.

出版信息

Fertil Steril. 1996 Nov;66(5):734-40. doi: 10.1016/s0015-0282(16)58627-0.

Abstract

OBJECTIVE

To evaluate the long-term efficacy of the 5 alpha-reductase inhibitor finasteride in idiopathic hirsutism.

DESIGN

Prospective clinical study.

SETTING

Outpatients in a university hospital.

PATIENT(S): Fourteen young women with idiopathic hirsutism.

INTERVENTION(S): Finasteride, 5 mg once daily, was given for 12 months.

MAIN OUTCOME MEASURE(S): Degree of hirsutism, graded by a modified Ferriman and Gallwey score, serum sex hormones, and serum and urinary markers of 5 alpha-reductase activity. Clinical outcome was evaluated up to and including the 1-year post-treatment period.

RESULT(S): The Ferriman and Gallwey score showed a remarkable reduction after 12 months of finasteride treatment (4.4 +/- 0.7 versus 11.8 +/- 1.0; mean +/- SEM). Serum levels of the two 5 alpha-reductase activity markers, dihydrotestosterone and 3 alpha-androstanediol glucuronide, decreased, and urinary C19 and C21 5 beta:5 alpha steroid metabolite ratios consistently increased during finasteride administration. These changes were reversed readily after cessation of treatment. No significant adverse effect was reported. Nine of 14 women completed the 1-year post-treatment follow-up. Their hirsutism scores were increased substantially as compared with values recorded at the end of therapy, but still were lower than baseline values.

CONCLUSION(S): The 5 alpha-reductase inhibitor finasteride is effective and well tolerated in longterm treatment of women with idiopathic hirsutism. Post-treatment follow-up suggests that drug effects on hair growth are sustained in the majority of subjects with this disorder.

摘要

目的

评估5α-还原酶抑制剂非那雄胺治疗特发性多毛症的长期疗效。

设计

前瞻性临床研究。

地点

大学医院门诊。

患者

14名患有特发性多毛症的年轻女性。

干预措施

给予非那雄胺5毫克,每日1次,共治疗12个月。

主要观察指标

多毛症程度(采用改良的费里曼和盖尔韦评分法分级)、血清性激素以及5α-还原酶活性的血清和尿液标志物。在治疗后长达1年的时间内评估临床结局。

结果

非那雄胺治疗12个月后,费里曼和盖尔韦评分显著降低(4.4±0.7对11.8±1.0;均值±标准误)。在服用非那雄胺期间,5α-还原酶活性的两个标志物——双氢睾酮和3α-雄烷二醇葡糖苷酸的血清水平降低,尿中C19和C21 5β:5α类固醇代谢物比值持续升高。治疗停止后,这些变化迅速逆转。未报告明显不良反应。14名女性中有9名完成了治疗后1年的随访。与治疗结束时记录的值相比,她们的多毛症评分大幅增加,但仍低于基线值。

结论

5α-还原酶抑制剂非那雄胺在长期治疗特发性多毛症女性中有效且耐受性良好。治疗后随访表明,该药物对大多数患有这种疾病的受试者的毛发生长有持续影响。

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