Green Stuart A, Alon Achilles, Ianus Juliana, McNaughton Kristin S, Tozzi Carol A, Reiss Theodore F
Respiratory & Allergy, Merck Research Laboratories, Merck & Co. Inc., 126 E. Lincoln Avenue, Rahway, NJ 07065, USA.
J Urol. 2006 Dec;176(6 Pt 1):2535-40; discussion 2540. doi: 10.1016/j.juro.2006.08.018.
Urge urinary incontinence is the involuntary leakage of urine commonly occurring in older adults, particularly women. Preclinical evidence suggests that urge urinary incontinence may occur due to up-regulation of tachykinin mediated bladder/spinal reflex signaling. This study tested the hypothesis that aprepitant, a neurokinin-1 receptor antagonist, may be efficacious in the treatment of urge urinary incontinence.
This was a double-blind, randomized, placebo controlled, parallel group pilot study in which postmenopausal women with a history of urge urinary incontinence or mixed incontinence (with predominantly urge urinary incontinence) were assigned to receive a 160 mg capsule of aprepitant (61) or placebo (64) once daily for 8 weeks. The primary end point was percent change from baseline in average daily micturitions assessed by a voiding diary. Secondary end points included average daily total urinary incontinence and urge urinary incontinence episodes, and urgency episodes.
Aprepitant significantly decreased the average daily number of micturitions compared with placebo at 8 weeks. The between-group treatment difference expressed as percent change from baseline was -6.8%, 95% CI (-12.5, -1.1) (p = 0.019). The average daily number of urgency episodes was also significantly reduced compared to placebo (p = 0.049). The average daily number of urge urinary incontinence and total urinary incontinence episodes were also reduced, although the difference was not statistically significant. Aprepitant was generally well tolerated and adverse experiences were generally mild.
Results of this initial study suggest that neurokinin-1 receptor antagonism may represent a novel therapeutic approach to treating overactive bladder syndrome.
急迫性尿失禁是老年人尤其是女性中常见的尿液不自主漏出。临床前证据表明,急迫性尿失禁可能是由于速激肽介导的膀胱/脊髓反射信号上调所致。本研究检验了阿瑞匹坦(一种神经激肽-1受体拮抗剂)可能有效治疗急迫性尿失禁的假设。
这是一项双盲、随机、安慰剂对照、平行组的试点研究,将有急迫性尿失禁病史或混合性尿失禁(以急迫性尿失禁为主)的绝经后女性分为两组,分别每日服用一次160毫克阿瑞匹坦胶囊(61例)或安慰剂(64例),持续8周。主要终点是通过排尿日记评估的平均每日排尿次数相对于基线的变化百分比。次要终点包括平均每日尿失禁和急迫性尿失禁发作的总数,以及尿急发作次数。
与安慰剂相比,8周时阿瑞匹坦显著减少了平均每日排尿次数。以相对于基线的变化百分比表示的组间治疗差异为-6.8%,95%置信区间为(-12.5,-1.1)(p = 0.019)。与安慰剂相比,平均每日尿急发作次数也显著减少(p = 0.049)。平均每日急迫性尿失禁和总尿失禁发作次数也有所减少,尽管差异无统计学意义。阿瑞匹坦总体耐受性良好,不良反应一般较轻。
这项初步研究的结果表明,神经激肽-1受体拮抗作用可能代表一种治疗膀胱过度活动症的新治疗方法。