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勃起功能障碍患者的内皮功能障碍:一项使用他达拉非的双盲随机对照试验

Endothelial Dysfunction in Patients With Erectile Dysfunction: A Double-Blind, Randomized-Control Trial Using Tadalafil.

作者信息

Pattanaik Smita, Kaundal Pawan, Mavuduru Ravimohan S, Singh Shrawan K, Mandal Arup K

机构信息

Department of Pharmacology, Postgraduate Institute of Medical Education and Research, Chandigarh, India; Department of Urology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Department of Urology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Sex Med. 2019 Mar;7(1):41-47. doi: 10.1016/j.esxm.2018.11.008. Epub 2019 Jan 9.

Abstract

OBJECTIVE

To assess whether tadalafil improves endothelial dysfunction(EnD) in a placebo-controlled randomized-control trial.

METHODS

Erectile dysfunction and EnD were assessed by the International Index of Erectile Function (IIEF-5) and flow-mediated dilation (FMD) of the brachial artery respectively, at baseline and 4 weeks by blinded observer. Patients with FMD of < 15% were randomized in 1:1 ratio to receive either placebo or tadalafil. Both placebo and tadalafil in similar-appearing capsules but coded separately, were dispensed by a blinded co-investigator. Compliance and drug-related events were recorded. The randomization codes were then decoded and appropriate statistical tests applied.

RESULTS

89 patients were randomized and 82 completed the study. Both groups were comparable. Posttreatment, there were significant improvements in IIEF-5 score (pre- vs posttreatment; tadalafil: 11.432 vs 15.937, P < .001 and placebo 11.232 vs 14.935, P < .00) and FMD% pre- vs posttreatment; tadalafil: 11.222 vs 13.827, P < .001 and placebo: 11.617 vs 14.027, P < .001). Intergroup comparison did not show any significant difference in IIEF scores (mean change in tadalafil vs placebo group: 3.719 vs 4.433, P = .223) and FMD% (mean change tadalafil vs placebo group: 2.426 and 2.829, P = .528). The adverse events were significantly more in the tadalafil group (tadalafil vs placebo 14 adverse reactions [ADR] vs 5 ADR, P < .001).

CONCLUSION

The response of low-dose tadalafil on IIEF and FMD is largely similar to placebo; however, the utility of FMD% in young patients and placebo effect needs to be studied further. Pattanaik S, Kaundal P, Mavuduru RS, et al. Endothelial Dysfunction in Patients With Erectile Dysfunction: A Double-Blind, Randomized-Control Trial Using Tadalafil. Sex Med 2019;7:41-47.

摘要

目的

在一项安慰剂对照的随机对照试验中评估他达拉非是否能改善内皮功能障碍(EnD)。

方法

在基线和4周时,由盲法观察者分别通过国际勃起功能指数(IIEF-5)和肱动脉血流介导的血管舒张(FMD)评估勃起功能障碍和EnD。FMD<15%的患者按1:1比例随机分组,分别接受安慰剂或他达拉非。安慰剂和他达拉非装在外观相似但单独编码的胶囊中,由盲法共同研究者分发。记录依从性和药物相关事件。然后对随机分组代码进行解码并应用适当的统计检验。

结果

89例患者被随机分组,82例完成研究。两组具有可比性。治疗后,IIEF-5评分(治疗前与治疗后;他达拉非:11.432对15.937,P<.001;安慰剂:11.232对14.935,P<.00)以及FMD%(治疗前与治疗后;他达拉非:11.222对13.827,P<.001;安慰剂:11.617对14.027,P<.001)均有显著改善。组间比较显示,IIEF评分(他达拉非组与安慰剂组的平均变化:3.719对4.433,P=.223)和FMD%(他达拉非组与安慰剂组的平均变化:2.426和2.829,P=.528)无显著差异。他达拉非组的不良事件明显更多(他达拉非组与安慰剂组分别有14例不良反应[ADR]对5例ADR,P<.001)。

结论

低剂量他达拉非对IIEF和FMD的反应与安慰剂基本相似;然而,FMD%在年轻患者中的效用以及安慰剂效应需要进一步研究。帕塔纳伊克S、坎达尔P、马武杜鲁RS等。勃起功能障碍患者的内皮功能障碍:一项使用他达拉非的双盲随机对照试验。《性医学》2019年;7:41 - 47。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fc0/6377381/dd0fc829109d/gr1.jpg

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