Four-strain probiotic exerts a positive effect on irritable bowel syndrome symptoms occurring in inflammatory bowel diseases in absence of inflammation (train-IBD trial).

Anne Fennessy, Micheal Doyle, Anna Boland, Rachel Bourke, Anthony O'Connor
{"title":"Four-strain probiotic exerts a positive effect on irritable bowel syndrome symptoms occurring in inflammatory bowel diseases in absence of inflammation (train-IBD trial).","authors":"Anne Fennessy, Micheal Doyle, Anna Boland, Rachel Bourke, Anthony O'Connor","doi":"10.4292/wjgpt.v16.i2.101268","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Irritable bowel syndrome (IBS) symptoms are common in patients with inflammatory bowel disease (IBD), with systematic review reporting an overall pooled prevalence of 35-39% in patients with clinical remission. This subset of patients reports a reduced quality of life and increased anxiety and depression. A multi-strain probiotic (Symprove™, Symprove Ltd, Farnham, United Kingdom) has been shown to improve overall symptom severity in patients with IBS and is associated with decreased intestinal inflammation in patients with ulcerative colitis (UC), but not in Crohn's disease (CD).</p><p><strong>Aim: </strong>To ascertain whether this multi-strain probiotic would be effective in an IBS/IBD overlap population.</p><p><strong>Methods: </strong>The treatment of symptoms in the absence of inflammation in inflammatory bowel diseases trial was a randomized, double-blind, placebo-controlled trial of a four-strain probiotic Symprove, containing Lactobacillus rhamnosus NCIMB 30174, Lactobacillus plantarum NCIMB 30173, Lactobacillus acidophilus NCIMB 30175 and Enterococcus faecium NCIMB 30176. The duration of the study was 3 months, at the end of which IBS-Symptom Severity Score (IBS-SSS) was repeated. Primary Endpoint was a 100-point reduction in IBS-SSS.</p><p><strong>Results: </strong>61 participants were randomized into the intention-to-treat analysis. 45% of patients receiving the active agent achieved the endpoint compared to 33% of those receiving placebo (<i>P</i> = 0.42). In UC, 50% of patients receiving placebo achieved the endpoint compared to 44% of those receiving the active agent (<i>P</i> = 1.00). In CD 45% of those receiving the active agent achieved the endpoint compared to 29% of those receiving placebo (<i>P</i> = 0.34). The mean change in IBS-SSS for patients receiving placebo was a reduction of 61 points, compared to a reduction in 90 points for patients receiving active agent (<i>P</i> = 0.31). There was no difference between the groups with regard to IBD outcomes.</p><p><strong>Conclusion: </strong>Probiotics may represent a safe and effective means of addressing the unmet clinical need for symptom relief in patients with overlapping IBS and IBD, especially in those with CD.</p>","PeriodicalId":60311,"journal":{"name":"世界胃肠药理与治疗学杂志:英文版(电子版)","volume":"16 2","pages":"101268"},"PeriodicalIF":0.0000,"publicationDate":"2025-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12188889/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"世界胃肠药理与治疗学杂志:英文版(电子版)","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.4292/wjgpt.v16.i2.101268","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Irritable bowel syndrome (IBS) symptoms are common in patients with inflammatory bowel disease (IBD), with systematic review reporting an overall pooled prevalence of 35-39% in patients with clinical remission. This subset of patients reports a reduced quality of life and increased anxiety and depression. A multi-strain probiotic (Symprove™, Symprove Ltd, Farnham, United Kingdom) has been shown to improve overall symptom severity in patients with IBS and is associated with decreased intestinal inflammation in patients with ulcerative colitis (UC), but not in Crohn's disease (CD).

Aim: To ascertain whether this multi-strain probiotic would be effective in an IBS/IBD overlap population.

Methods: The treatment of symptoms in the absence of inflammation in inflammatory bowel diseases trial was a randomized, double-blind, placebo-controlled trial of a four-strain probiotic Symprove, containing Lactobacillus rhamnosus NCIMB 30174, Lactobacillus plantarum NCIMB 30173, Lactobacillus acidophilus NCIMB 30175 and Enterococcus faecium NCIMB 30176. The duration of the study was 3 months, at the end of which IBS-Symptom Severity Score (IBS-SSS) was repeated. Primary Endpoint was a 100-point reduction in IBS-SSS.

Results: 61 participants were randomized into the intention-to-treat analysis. 45% of patients receiving the active agent achieved the endpoint compared to 33% of those receiving placebo (P = 0.42). In UC, 50% of patients receiving placebo achieved the endpoint compared to 44% of those receiving the active agent (P = 1.00). In CD 45% of those receiving the active agent achieved the endpoint compared to 29% of those receiving placebo (P = 0.34). The mean change in IBS-SSS for patients receiving placebo was a reduction of 61 points, compared to a reduction in 90 points for patients receiving active agent (P = 0.31). There was no difference between the groups with regard to IBD outcomes.

Conclusion: Probiotics may represent a safe and effective means of addressing the unmet clinical need for symptom relief in patients with overlapping IBS and IBD, especially in those with CD.

四菌株益生菌对炎症性肠病在无炎症的情况下发生的肠易激综合征症状有积极作用(训练- ibd试验)。
背景:肠易激综合征(IBS)症状在炎症性肠病(IBD)患者中很常见,系统评价报告临床缓解患者的总体总患病率为35-39%。这部分患者报告生活质量下降,焦虑和抑郁增加。一种多菌株益生菌(Symprove™,Symprove Ltd, Farnham, uk)已被证明可以改善IBS患者的整体症状严重程度,并与溃疡性结肠炎(UC)患者的肠道炎症减少相关,但与克罗恩病(CD)患者无关。目的:确定该多菌株益生菌对IBS/IBD重叠人群是否有效。方法:治疗炎症性肠病无炎症症状的试验是一项随机、双盲、安慰剂对照的四菌株益生菌Symprove试验,其中含有鼠李糖乳杆菌NCIMB 30174、植物乳杆菌NCIMB 30173、嗜酸乳杆菌NCIMB 30175和屎肠球菌NCIMB 30176。研究持续时间为3个月,研究结束时重复ibs -症状严重程度评分(IBS-SSS)。主要终点是IBS-SSS降低100分。结果:61名参与者被随机纳入意向治疗分析。45%接受活性药物治疗的患者达到终点,而33%接受安慰剂治疗的患者达到终点(P = 0.42)。在UC中,接受安慰剂治疗的患者达到终点的比例为50%,而接受药物治疗的患者达到终点的比例为44% (P = 1.00)。在CD中,45%的接受活性药物治疗的患者达到了终点,而29%的接受安慰剂治疗的患者达到了终点(P = 0.34)。接受安慰剂的患者IBS-SSS的平均变化减少了61分,而接受活性药物的患者减少了90分(P = 0.31)。在IBD结果方面,两组之间没有差异。结论:益生菌可能是解决IBS和IBD重叠患者未满足的临床症状缓解需求的一种安全有效的手段,特别是对乳糜泻患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
300
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信