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5α还原酶抑制剂与勃起功能障碍:二者的关联

5-alpha reductase inhibitors and erectile dysfunction: the connection.

作者信息

Erdemir Fikret, Harbin Andrew, Hellstrom Wayne J G

机构信息

Tulane University-Department of Urology, New Orleans, LA, USA.

出版信息

J Sex Med. 2008 Dec;5(12):2917-24. doi: 10.1111/j.1743-6109.2008.01001.x.

Abstract

INTRODUCTION

Benign prostatic hyperplasia (BPH) is a common problem affecting middle-aged and elderly men. First-line medical therapy includes alpha 1blockers and 5alpha-reductase inhibitors (5ARIs), such as finasteride and dutasteride. 5ARI use has been associated with adverse sexual outcomes, including erectile dysfunction (ED), ejaculatory dysfunction (EjD), and decreased libido.

AIM

To clarify the association between sexual adverse effects (AEs) and 5ARIs through review of literature concerning 5ARIs and to review the proposed mechanisms of these effects.

METHODS

A comprehensive literature review, using MEDLINE and PUBMED search engines, was conducted for all publications concerning 5ARIs and sexual AEs.

MAIN OUTCOME MEASURE

Sexual adverse effects, such as ED, EjD, and decreased libido, were the measured outcomes of this literature review.

RESULTS

Sexual AEs are reported in clinical trials at rates of 2.1% to 38%. The most common sexual AE is ED, followed by EjD and decreased libido. These effects occur early in therapy and attenuate over time. A proposed mechanism for sexual dysfunction involves decreased nitric oxide synthase activity due to decreased dihydrotestosterone.

CONCLUSIONS

The connection between 5ARIs and sexual dysfunction is apparent upon review of the literature. Though theories have been proposed, little is known about the exact mechanisms behind 5ARI-related sexual dysfunction. Since the connection between 5ARIs and sexual AEs is established in the literature, future research should be directed toward deciphering the pathophysiologic mechanisms. When more basic science knowledge is attained in this area, the focus can shift toward prevention and treatment.

摘要

引言

良性前列腺增生(BPH)是影响中老年男性的常见问题。一线药物治疗包括α1受体阻滞剂和5α-还原酶抑制剂(5ARIs),如非那雄胺和度他雄胺。使用5ARIs与不良性结局有关,包括勃起功能障碍(ED)、射精功能障碍(EjD)和性欲减退。

目的

通过回顾有关5ARIs的文献,阐明性不良反应(AEs)与5ARIs之间的关联,并综述这些效应的潜在机制。

方法

使用MEDLINE和PUBMED搜索引擎对所有有关5ARIs和性AEs的出版物进行全面的文献综述。

主要观察指标

勃起功能障碍、射精功能障碍和性欲减退等性不良反应是本次文献综述的观察指标。

结果

临床试验中报道的性AEs发生率为2.1%至38%。最常见的性AE是ED,其次是EjD和性欲减退。这些效应在治疗早期出现,并随时间减弱。性功能障碍的一种潜在机制是由于二氢睾酮减少导致一氧化氮合酶活性降低。

结论

回顾文献后,5ARIs与性功能障碍之间的联系显而易见。尽管已经提出了一些理论,但对于5ARI相关性性功能障碍背后的确切机制知之甚少。由于5ARIs与性AEs之间的联系在文献中已得到证实,未来的研究应致力于阐明其病理生理机制。当在该领域获得更多基础科学知识时,重点可转向预防和治疗。

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