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非那雄胺而非坦索罗辛会加重良性前列腺增生男性的勃起功能障碍严重程度并降低睾酮水平。

Finasteride, not tamsulosin, increases severity of erectile dysfunction and decreases testosterone levels in men with benign prostatic hyperplasia.

作者信息

Traish Abdulmaged M, Haider Karim Sultan, Doros Gheorghe, Haider Ahmad

出版信息

Horm Mol Biol Clin Investig. 2015 Sep;23(3):85-96. doi: 10.1515/hmbci-2015-0015.

Abstract

BACKGROUND

5α-reductase inhibitors (5α-RIs) (finasteride and dutasteride) have been proven useful in treatment of lower urinary tract symptoms (LUTS) related to benign prostatic hyperplasia (BPH). However, these inhibitors exert undesirable sexual side effects and, in some cases, these effects are persistent. There is considerable disagreement with regard to whether the adverse side effects resolve with continuous treatment.

AIM

To investigate the long-term adverse effects of finasteride treatment in men with BPH on erectile function and to compare these adverse effects in men treated with the α1-adrenergic receptor blocker, tamsolusin.

METHODS

In this retrospective registry study, a cohort of 470 men aged between 47 and 68 years (mean 57.78±4.81) were treated with finasteride (5 mg/day). A second cohort of 230 men aged between 52 and 72 years (mean 62.62±4.65) were treated with tamsulosin (0.4 mg). All men were followed up for 45 months. At intervals of 3 months and at each visit, plasma testosterone (T) levels and the international index of erectile function (IIEF-EF) questionnaire scores were determined.

RESULTS

Long-term treatment with finasteride therapy is associated with worsening of erectile dysfunction (ED) as shown by the significant decrease in the IIEF-EF scores in men treated with finasteride. No worsening of ED was observed in men treated with tamsulosin. The increase in ED due to finasteride did not resolve with continued treatment with finasteride. Most importantly, long-term finasteride therapy resulted in reduction in total T levels, contributing to a state of hypogonadism. On the contrary, no changes in T levels were noted in men treated with tamsolusin.

CONCLUSION

Our findings suggest that in men with BPH, long-term finasteride therapy but not tamsulosin results in worsening of ED and reduces total T concentrations. Clinicians are urged to discuss the impact of 5α-RIs therapy on sexual function with their patients before commencing this therapy.

摘要

背景

5α-还原酶抑制剂(5α-RIs)(非那雄胺和度他雄胺)已被证实可有效治疗与良性前列腺增生(BPH)相关的下尿路症状(LUTS)。然而,这些抑制剂会产生不良的性功能副作用,并且在某些情况下,这些影响会持续存在。关于这些副作用是否会随着持续治疗而缓解,存在相当大的分歧。

目的

研究非那雄胺治疗BPH男性对勃起功能的长期不良影响,并比较其与α1-肾上腺素能受体阻滞剂坦索罗辛治疗男性的这些不良反应。

方法

在这项回顾性登记研究中,一组470名年龄在47至68岁(平均57.78±4.81岁)的男性接受非那雄胺(5毫克/天)治疗。另一组230名年龄在52至72岁(平均62.62±4.65岁)的男性接受坦索罗辛(0.4毫克)治疗。所有男性均随访45个月。每隔3个月及每次就诊时,测定血浆睾酮(T)水平和国际勃起功能指数(IIEF-EF)问卷评分。

结果

如接受非那雄胺治疗男性的IIEF-EF评分显著降低所示,非那雄胺长期治疗与勃起功能障碍(ED)恶化相关。接受坦索罗辛治疗的男性未观察到ED恶化。非那雄胺所致的ED增加并未随着继续使用非那雄胺治疗而缓解。最重要的是,非那雄胺长期治疗导致总T水平降低,导致性腺功能减退状态。相反,接受坦索罗辛治疗的男性T水平未发现变化。

结论

我们的研究结果表明,在BPH男性中,长期使用非那雄胺治疗而非坦索罗辛会导致ED恶化并降低总T浓度。敦促临床医生在开始这种治疗之前,与患者讨论5α-RIs治疗对性功能的影响。

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