Rabasseda Xavier
Medical Information Department, Prous Science, Barcelona, Spain.
Drugs Today (Barc). 2004 Aug;40(8):649-61. doi: 10.1358/dot.2004.40.8.850468.
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.
度他雄胺是一种5α-还原酶抑制剂,可抑制5α-还原酶的1型和2型同工酶,该酶负责在前列腺和其他组织中将睾酮转化为二氢睾酮。二氢睾酮是前列腺生长的主要原因,并且已被证明在良性前列腺增生的发生和发展中起关键作用。度他雄胺已在三项多中心研究中进行了调查,这些研究涉及4325名年龄在50岁及以上的患有良性前列腺增生的男性。这些为期两年、安慰剂对照研究的数据表明,每日一次服用0.5mg度他雄胺可降低急性尿潴留风险以及与良性前列腺增生相关的手术干预需求,改善与良性前列腺增生相关的症状,减小前列腺体积并增加最大尿流率,且一般轻度至中度不良事件的发生率较低。