Canguven Onder, Burnett Arthur L
The Johns Hopkins Hospital, The James Buchanan Brady Urological Institute, Department of Urology, Marburg 414, 600 North Wolfe Street, Baltimore, MD 21287, USA.
J Androl. 2008 Sep-Oct;29(5):514-23. doi: 10.2164/jandrol.108.005025. Epub 2008 Apr 17.
The 5 alpha-reductase inhibitors, which inhibit conversion of testosterone to dihydrotestosterone, are used for miscellaneous clinical applications, including the treatment of benign prostatic hyperplasia and male pattern hair loss, and for possible reduction of the risk of prostate cancer. Erectile dysfunction has been associated with 5 alpha-reductase inhibitors. Overall, reports in the literature suggest rates of erectile dysfunction to be between 0.8%-33% in men using these medications. However, randomized controlled studies report the rates of erectile dysfunction to be between 0.8%-15.8%. The possible risk association is that these medications impact androgen function, which is understood to contribute to normal erectile physiology. The 5 alpha-reductase inhibitors result in a drop in median serum dihydrotestosterone levels by 60%-93% within 2 years, but there is no major change in testosterone levels. In this review, we surveyed studies on erectile dysfunction in patients treated with 5 alpha-reductase inhibitors and critically examined the evidence that associates 5 alpha-reductase inhibitors and erectile dysfunction. We conclude that 5 alpha-reductase inhibitors do not lead to erectile dysfunction to a significant degree, and we support the position that dihydrotestosterone is less relevant than testosterone in erectile function.
5α-还原酶抑制剂可抑制睾酮转化为双氢睾酮,用于多种临床应用,包括治疗良性前列腺增生和男性型脱发,以及可能降低前列腺癌风险。勃起功能障碍与5α-还原酶抑制剂有关。总体而言,文献报道使用这些药物的男性勃起功能障碍发生率在0.8%-33%之间。然而,随机对照研究报告勃起功能障碍发生率在0.8%-15.8%之间。可能的风险关联是这些药物会影响雄激素功能,而雄激素功能被认为对正常勃起生理有作用。5α-还原酶抑制剂可使血清双氢睾酮中位数水平在2年内下降60%-93%,但睾酮水平无重大变化。在本综述中,我们调查了接受5α-还原酶抑制剂治疗的患者勃起功能障碍的研究,并严格审查了将5α-还原酶抑制剂与勃起功能障碍相关联的证据。我们得出结论,5α-还原酶抑制剂不会在很大程度上导致勃起功能障碍,并且我们支持双氢睾酮在勃起功能中比睾酮相关性更低的观点。