An update on the use of 5α-reductase inhibitors

被引:4
作者
Foley, CL
Bott, SRJ
Shergill, IS
Kirby, RS
机构
[1] UCL, Inst Urol & Nephrol, London, England
[2] Univ London St Georges Hosp, Sch Med, London SW17 0RE, England
关键词
D O I
10.1358/dot.2004.40.3.820085
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Twelve years ago, finasteride, the first 5alpha-reductase inhibitor, was introduced as drug therapy for benign prostatic hyperplasia, and more recently dutasteride has emerged as an alternative. The efficacy, safety and ability of these 5(C)-reductase inhibitors to reverse the natural progression of benign prostatic hyperplasia have been convincingly demonstrated and both drugs are now well established in the medical armamentarium against the disease. Given the multifactorial etiology of benign hyperplasia, the usefulness of 5(C)-reductase inhibitors in combination with a adrenergic blockers has also been investigated and justified in select patients. Wider applications of 5(C)-reductase inhibitors are also emerging, though their perhaps most important new role as chemopreventive agents remains unclear. (C) 2004 Prous Science. All rights reserved.
引用
收藏
页码:213 / 223
页数:11
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