Deiana Simona, Gabbani Tommaso, Bagnoli Siro, Annese Vito
Emergency Department, Gastroenterology SOD2, AOU Careggi , Florence , Italy +39 55 7946035 ;
Expert Opin Emerg Drugs. 2015 Jun;20(2):247-61. doi: 10.1517/14728214.2015.1013935. Epub 2015 Mar 3.
Irritable bowel syndrome (IBS) is one of the most common gastrointestinal disorders with a 9 - 23% prevalence estimated in the general population. Patients can be subdivided into those who tend to have predominant diarrhea (IBS-D) or predominant constipation (IBS-C). Total annual productivity loss related to IBS in US is estimated at $205 million, with a significant impairment of health-related quality of life. A gold standard for the treatment of IBS is not established. Symptoms might improve with the use of few drugs and behavioral therapy, however, data concerning efficacy, safety and tolerability are limited. Therefore, development and validation of new therapies targeting at the molecular level are widely awaited.
We will specifically describe in this review Phase II and Phase III trials, with specific focus on treatment of IBS-D patients. Unfortunately, it is difficult to draw definite conclusions from Phase II and Phase III trials, because of the known high placebo effect.
Drugs active on opioid receptor subtypes and neurokinin (NK) receptors seem to be the most promising, but substantial progress of information in this field is still needed. The achievement of more insights on the pathogenesis of IBS could surely better drive and target the therapy, but still strong efforts are awaited.
肠易激综合征(IBS)是最常见的胃肠道疾病之一,普通人群中的患病率估计为9%-23%。患者可分为以腹泻为主型(IBS-D)或以便秘为主型(IBS-C)。据估计,美国每年因IBS导致的生产力损失总计达2.05亿美元,对健康相关生活质量有显著损害。IBS的治疗尚无金标准。使用少数药物和行为疗法症状可能改善,然而,关于疗效、安全性和耐受性的数据有限。因此,迫切需要开发和验证针对分子水平的新疗法。
在本综述中,我们将具体描述II期和III期试验,特别关注IBS-D患者的治疗。不幸的是,由于已知的高安慰剂效应,很难从II期和III期试验中得出明确结论。
对阿片受体亚型和神经激肽(NK)受体有活性的药物似乎最有前景,但该领域仍需大量信息进展。对IBS发病机制有更多深入了解肯定能更好地推动和靶向治疗,但仍需付出巨大努力。