Dutasteride -: A potent dual inhibitor of 5α-reductase for benign prostatic hyperplasia

被引:4
|
作者
Rabasseda, X [1 ]
机构
[1] Prous Sci, Dept Med Informat, Barcelona 08025, Spain
关键词
D O I
10.1358/dot.2004.40.8.850468
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dutasteride is a 5alpha-reductase inhibitor that inhibits both types 1 and 2 isozymes of 5alpha-reductase, the enzyme responsible for converting testosterone to dihydrotestosterone in the prostate and other tissues. Dihydrotestosterone is the primary cause of prostate growth and has been proven to play a key role in the development and progression of benign prostatic hyperplasia. Dutasteride has been investigated in three multicenter studies involving 4325 men aged 50 years and above with benign prostatic hyperplasia. Data from these two-year, placebo-controlled studies demonstrated that dutasteride 0.5 mg once daily reduced the risk of both acute urinary retention and the need for benign prostatic hyperplasia-related surgical intervention, improved benign prostatic hyperplasia-related symptoms, decreased prostate volume and increased maximum urinary flow rates with a low incidence of generally mild to moderate adverse events. (C) 2004 Prous Science. All rights reserved.
引用
收藏
页码:649 / 661
页数:13
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