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治疗膀胱过度活动症的潜在药物治疗方法。

Prospective pharmacologic therapies for the overactive bladder.

机构信息

Wake Forest Institute for Regenerative Medicine, Wake Forest University School of Medicine, Medical Center Boulevard, Winston Salem, NC 27157, USA.

出版信息

Ther Adv Urol. 2009 Jun;1(2):71-83. doi: 10.1177/1756287209103937.

Abstract

Lower urinary tract symptoms (LUTS), overactive bladder syndrome (OAB) and detrusor overactivity (DO) are all conditions that can have major effects on quality of life and social functioning. Antimuscarinic drugs are first-line treatment-they often have good initial response rates, but adverse effects and decreasing efficacy cause long-term compliance problems, and alternatives are needed. The recognition of the functional contribution of the urothelium, the spontaneous myocyte activity during bladder filling, and the diversity of nerve transmitters has sparked interest in both peripheral and central modulation of LUTS/OAB/DO pathophysiology. There may be several new possibilities to treat LUTS/OAB/DO. β(3)-AR agonists (YM178), PDE 5 inhibitors (sildenafil, tadalafil, vardenafil), vitamin D analogs (elocalcitol), combinations (α(1)-AR antagonist + antimuscarinic), and drugs with a central mode of action (tramadol, aprepitant) all have Randomized controlled trial (RCT) documented efficacy. Which of these therapeutic principles will be developed to clinically useful treatments remains to be established.

摘要

下尿路症状(LUTS)、膀胱过度活动症(OAB)和逼尿肌过度活动(DO)都会对生活质量和社会功能产生重大影响。抗毒蕈碱药物是一线治疗药物——它们通常具有良好的初始反应率,但不良反应和疗效下降会导致长期依从性问题,因此需要替代品。尿路上皮的功能贡献、膀胱充盈期间自发性肌细胞活动以及神经递质的多样性,激发了人们对 LUTS/OAB/DO 病理生理学的外周和中枢调节的兴趣。治疗 LUTS/OAB/DO 可能有几种新的可能性。β(3)-AR 激动剂(YM178)、PDE5 抑制剂(西地那非、他达拉非、伐地那非)、维生素 D 类似物(依他钙醇)、联合用药(α(1)-AR 拮抗剂+抗毒蕈碱药物)和具有中枢作用模式的药物(曲马多、阿瑞匹坦)都有随机对照试验(RCT)证明其疗效。这些治疗原则中的哪一种将被开发为临床有用的治疗方法还有待确定。

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