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Tadalafil for lower urinary tract symptoms secondary to benign prostatic hyperplasia: a review of clinical data in Asian men and an update on the mechanism of action

机译:他达拉非治疗良性前列腺增生继发的下尿路症状:亚洲男性临床资料回顾及作用机制的最新进展

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Tadalafil, a phosphodiesterase type 5 (PDE5) inhibitor, is approved worldwide for the treatment of lower urinary tract symptoms secondary to benign prostatic hyperplasia (BPH-LUTS). The purpose of this narrative review is to summarize the clinical data on tadalafil 5 mg once-daily, primarily focusing on Asian men with BPH-LUTS, and to update the current understanding of the mechanism of action underlying PDE5 inhibition. Findings from studies have demonstrated that PDE5 is highly expressed in the lower urinary tract and supporting vasculature, and that PDE5 inhibition potentially decreases smooth muscle cell proliferation in the prostate, relaxes smooth muscle in the prostate, bladder neck and supporting vasculature, increases blood perfusion to the lower urinary tract, and modulates bladder afferent nerve activity. A total of 11 larger, 12-week, double-blind, randomized, placebo-controlled studies of tadalafil, including four Asian studies, have been conducted globally, enrolling 3000 men with BPH-LUTS. In addition, two long-term (42- and 52-week) studies enrolled 394 Japanese and 428 North American men, respectively, with BPH-LUTS. Overall, tadalafil 5 mg once-daily resulted in significant improvements in the change from baseline to endpoint in total International Prostate Symptom Scores (IPSS), IPSS storage and voiding subscores, and IPSS quality of life index compared with placebo. Tadalafil was well tolerated and had a favorable safety profile. These findings support tadalafil 5 mg once-daily for treating men, including Asian men, with BPH-LUTS.
机译:他达拉非是一种5型磷酸二酯酶(PDE5)抑制剂,已在全球范围内被批准用于治疗继发于前列腺增生症(BPH-LUTS)的下尿路症状。这篇叙述性综述的目的是总结每天使用一次他达拉非5 mg的临床数据,主要针对患有BPH-LUTS的亚洲男性,并更新对PDE5抑制作用机理的最新了解。研究发现,PDE5在下尿路和支持性脉管系统中高度表达,PDE5的抑制作用可能会降低前列腺中的平滑肌细胞增殖,使前列腺,膀胱颈和支持性脉管系统中的平滑肌松弛,并增加对下泌尿道,并调节膀胱传入神经活动。他达拉非总共进行了11项较大的,为期12周,双盲,随机,安慰剂对照的研究,其中包括4项亚洲研究,在全球范围内招募了3000多名BPH-LUTS男性。此外,两项长期(42周和52周)研究分别使用BPH-LUTS纳入了394名日本男性和428名北美男性。总体而言,他达拉非5 mg每天一次,与安慰剂相比,国际前列腺症状总评分(IPSS),IPSS储存和排尿分值以及IPSS生活质量指数从基线到终点的变化显着改善。他达拉非的耐受性良好,安全性良好。这些发现支持他达拉非5 mg每天一次,用于治疗包括亚洲男性在内的男性BPH-LUTS。

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