Suppr超能文献

多毛症的治疗:具有中枢和外周作用的不同抗雄激素药物之间的比较

Treatment of hirsutism: comparisons between different antiandrogens with central and peripheral effects.

作者信息

Fruzzetti F, Bersi C, Parrini D, Ricci C, Genazzani A R

机构信息

Department of Reproductive Medicine, University of Pisa, Italy.

出版信息

Fertil Steril. 1999 Mar;71(3):445-51. doi: 10.1016/s0015-0282(98)00486-5.

Abstract

OBJECTIVE

To compare the clinical and endocrinologic effects of cyproterone acetate (CPA), an antiandrogen with progestational activity; flutamide, a nonsteroidal antiandrogen, and finasteride, an inhibitor of 5alpha-reductase.

DESIGN

Randomized, open, controlled clinical study.

SETTING

Department of Obstetrics and Gynecology, University of Pisa, Pisa, Italy.

PATIENT(S): Forty-five hirsute women were enrolled in the study: 29 were hyperandrogenic and 16 had idiopathic hirsutism. Three women dropped out of the study.

INTERVENTION(S): Women were randomly treated with finasteride (5 mg/d; n = 14), CPA (25 mg plus ethinyl E2 (EE); n = 13), or flutamide (500 mg/d; n = 15) for 1 year.

MAIN OUTCOME MEASURE(S): Hirsutism was assessed using the Ferriman-Gallwey method. Levels of total and free T, androstenedione (A), DHEAS, sex hormone-binding globulin, dihydrotestosterone, and 3alpha-androstanediol glucuronide were evaluated at the beginning of the study and every 3 months.

RESULT(S): Treatment with finasteride, flutamide, and CPA significantly decreased the Ferriman-Gallwey score. The percent decreases in the hirsutism score induced by the different treatments were similar. Treatment with CPA plus EE significantly decreased levels of total and free T, A, dihydrotestosterone, and 3alpha-androstanediol glucuronide. These parameters were unchanged with flutamide therapy. Finasteride significantly increased total T levels but reduced dihydrotestosterone and 3alpha-androstanediol glucuronide concentrations.

CONCLUSION(S): Finasteride, CPA, and flutamide are equally effective in decreasing hirsutism, despite different mechanisms of action.

摘要

目的

比较具有孕激素活性的抗雄激素药物醋酸环丙孕酮(CPA)、非甾体类抗雄激素药物氟他胺和5α-还原酶抑制剂非那雄胺的临床及内分泌效应。

设计

随机、开放、对照临床研究。

地点

意大利比萨大学妇产科。

患者

45名多毛女性纳入研究:29名高雄激素血症患者,16名特发性多毛患者。3名女性退出研究。

干预措施

女性被随机给予非那雄胺(5mg/d;n = 14)、CPA(25mg加乙炔雌二醇(EE);n = 13)或氟他胺(500mg/d;n = 15)治疗1年。

主要观察指标

采用费里曼-盖尔韦方法评估多毛情况。在研究开始时及每3个月评估总睾酮、游离睾酮、雄烯二酮(A)、硫酸脱氢表雄酮、性激素结合球蛋白、双氢睾酮和3α-雄烷二醇葡糖苷酸水平。

结果

非那雄胺、氟他胺和CPA治疗均显著降低费里曼-盖尔韦评分。不同治疗引起的多毛评分降低百分比相似。CPA加EE治疗显著降低总睾酮、游离睾酮、A、双氢睾酮和3α-雄烷二醇葡糖苷酸水平。氟他胺治疗这些参数无变化。非那雄胺显著提高总睾酮水平,但降低双氢睾酮和3α-雄烷二醇葡糖苷酸浓度。

结论

尽管作用机制不同,但非那雄胺、CPA和氟他胺在减少多毛方面同样有效。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验