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5-羟色胺3型受体拮抗剂雷莫司琼对静止期炎症性肠病患者腹泻型肠易激综合征(IBS-D)样症状的疗效:一项随机、双盲、安慰剂对照试验

Efficacy of Serotonin Type 3 Receptor Antagonist Ramosetron on Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D)-Like Symptoms in Patients with Quiescent Inflammatory Bowel Disease: A Randomized, Double-Blind, Placebo-Controlled Trial.

作者信息

Tomita Toshihiko, Fukui Hirokazu, Morishita Daisuke, Mori Sumire, Oshima Tadayuki, Shinzaki Shinichiro, Miwa Hiroto

机构信息

Division of Gastroenterology and Hepatology, Department of Internal Medicine, Hyogo Medical University, Nishinomiya 663-8501, Japan.

出版信息

J Clin Med. 2022 Nov 22;11(23):6882. doi: 10.3390/jcm11236882.

Abstract

Patients with quiescent inflammatory bowel disease (IBD) frequently suffer diarrhea-predominant irritable bowel syndrome (IBS-D)-like symptoms, such as abdominal pain or stool irregularities. Here, we assessed the effect of ramosetron, a serotonin type 3 (5-HT) receptor antagonist, on IBS-D-like symptoms in patients with quiescent IBD. Seventy patients with quiescent IBD, who met the Rome III diagnostic criteria for IBS-D, were randomly assigned to receive either ramosetron (5 μg; n = 35) or a placebo (n = 35) orally once daily for 4 weeks. The primary endpoint was the responder rate for global assessment of relief from overall IBS-D-like symptoms. The responder rates for relief of abdominal pain/discomfort and improvement of bowel habits were also evaluated. The responder rate for relief from overall IBS-D-like symptoms at the final evaluation point was significantly higher in the ramosetron group (35.5%) than in the placebo group (11.4%) ( = 0.037). The responder rate for improvement of bowel habits was significantly higher in the ramosetron group (38.7%) than in the placebo group (14.3%) ( = 0.028). The reduction of stool frequency was significantly greater in the ramosetron group than in the placebo group ( = 0.044). Ramosetron is effective for relief of overall IBS-D-like symptoms in patients with quiescent IBD.

摘要

静止期炎症性肠病(IBD)患者常出现以腹泻为主的肠易激综合征(IBS-D)样症状,如腹痛或大便异常。在此,我们评估了5-羟色胺3(5-HT)受体拮抗剂雷莫司琼对静止期IBD患者IBS-D样症状的影响。70例符合IBS-D罗马III诊断标准的静止期IBD患者被随机分配,分别口服雷莫司琼(5μg;n = 35)或安慰剂(n = 35),每日1次,共4周。主要终点是对总体IBS-D样症状缓解情况进行整体评估的缓解率。还评估了腹痛/不适缓解和排便习惯改善的缓解率。在最终评估点,雷莫司琼组总体IBS-D样症状缓解的缓解率(35.5%)显著高于安慰剂组(11.4%)(P = 0.037)。雷莫司琼组排便习惯改善的缓解率(38.7%)显著高于安慰剂组(14.3%)(P = 0.028)。雷莫司琼组大便频率的降低显著大于安慰剂组(P = 0.044)。雷莫司琼对缓解静止期IBD患者的总体IBS-D样症状有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20be/9736938/bbb0bdd5974a/jcm-11-06882-g001.jpg

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