用螺内酯治疗多毛症

Roland R. Tremblay
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引用次数: 48

摘要

具有抗雄激素活性的化合物的发现已导致其用于治疗各种病因的多毛症。螺内酯通常通过改变血浆睾酮的形成和代谢以及降低其血液生成速率来降低血浆睾酮;这种药物还有助于增加睾酮向雌二醇的外周转化。螺内酯的主要作用是抑制雄激素与细胞质或靶组织(如皮肤)细胞核中的受体分子的结合。在过去的五年中,我们研究了超过450例多毛症。这些妇女中约80%单独使用螺内酯或联合使用地塞米松(2.5%)或口服避孕药(15%)。根据Lorenzo(1970),多毛症被分类。在至少3到4年的研究中,80%的患者观察到良好到非常好的临床结果。本组患者中记录的不良副作用不到5%。根据我们的数据和我们的临床经验,我们得出结论,螺内酯是治疗女性多毛症的有效药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
10 Treatment of hirsutism with spironolactone

The discovery of compounds possessing antiandrogenic activities has led to their utilization in the treatment of hirsutism of various aetiologies. Spironolactone generally lowers the plasma testosterone by altering its formation and metabolism as well as by decreasing its blood production rate; the medication also contributes to increase the peripheral conversion of testosterone to oestradiol. A major action is that spironolactone inhibits androgen binding to receptor molecules in the cytosol or the nucleus of target tissues such as the skin. During the last five years, we have studied over 450 cases of hirsutism. Approximately 80% of these women were treated with spironolactone alone or in association with dexamethasone (2.5%) or an oral contraceptive (15%). Hirsutism was classified according to Lorenzo (1970). Good to very good clinical results were observed in 80% of the patients who were under study for a minimum of 3 to 4 years. Adverse side-effects were recorded in less than 5% of our group of patients. On the basis of our data and our clinical experience, we conclude that spironolactone is an effective drug in the treatment of female hirsutism.

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