J Acad Nutr Diet. 2020 Apr;120(4):565-586. doi: 10.1016/j.jand.2019.05.015. Epub 2019 Aug 28.
Irritable bowel syndrome (IBS) is the most common functional digestive condition in the industrialized world. The gut microbiota plays a key role in disease pathogenesis.
A systematic review and meta-analysis on case-control studies was conducted to determine whether there is gut microbial dysbiosis in participants with IBS in comparison with healthy controls and, if so, whether the dysbiosis pattern differs among IBS subtypes and geographic regions.
This review was conducted and reported according to the MOOSE (Meta-Analysis of Observational Studies in Epidemiology) 2000 and PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) 2009 guidelines. Research articles published up to May 9, 2018 were identified through MEDLINE (PubMed), Cochrane Central Register of Controlled Trials (Cochrane Library), ClinicalTrials.gov, EMBASE, and Web of Science. Study quality was assessed using the Newcastle-Ottawa Scale. Case-control studies of participants with IBS who had undergone quantitative gut microbial stool analysis were included. The primary exposure measure of interest is log bacterial counts per gram of stool. Meta-analyses were performed to estimate the mean difference (MD) in gut microbiota between participants with IBS and healthy controls using the random-effects model with inverse variance in Revman 5.3 and R 3.5.1. Publication bias was assessed with funnel plots and Egger's test. Between-study heterogeneity was analyzed using Higgins I statistic with 95% CIs.
There were 6,333 unique articles identified; 52 qualified for full-text screening. Of these, 23 studies were included for analysis (n=1,340 participants from North America, Europe, and Asia). Overall, the studies were moderate in quality. Comparing participants with IBS to healthy controls, lower fecal Lactobacillus (MD= -0.57 log colony-forming unit [CFU]/g; P<0.01) and Bifidobacterium (MD= -1.04 logCFU/g; P<0.01), higher Escherichia coli (MD=0.60 logCFU/g; P<0.01), and marginally higher Enterobacter (MD=0.74 logCFU/g; P=0.05). No difference was found between participants with IBS and healthy controls in fecal Bacteroides and Enterococcus (P=0.18 and 0.68, respectively). Publication bias was not observed except in Bifidobacterium (P=0.015). Subgroup analyses on participants with diarrhea-predominant and constipation-predominant IBS showed consistent results with the primary results. A subgroup analysis of Chinese studies was consistent with the primary results, except for fecal Bacteroides, which was increased in participants with IBS vs healthy controls (MD=0.29; 95% CI 0.13 to 0.46; P<0.01). Although substantial heterogeneity was detected (I>75%) in most comparisons, the direction of the effect estimates is relatively consistent across studies.
IBS is characterized by gut microbial dysbiosis. Prospective, large-scale studies are needed to delineate how gut microbial profiles can be used to guide targeted therapies in this challenging patient population.
肠易激综合征(IBS)是工业化世界最常见的功能性消化疾病。肠道微生物群在疾病发病机制中起着关键作用。
对病例对照研究进行系统评价和荟萃分析,以确定 IBS 患者与健康对照组相比是否存在肠道微生物失调,如果存在,IBS 亚型和地理区域之间的失调模式是否不同。
本综述根据 MOOSE(流行病学观察性研究的荟萃分析)2000 年和 PRISMA(系统评价和荟萃分析的首选报告项目)2009 年指南进行。通过 MEDLINE(PubMed)、Cochrane 中央对照试验注册中心(Cochrane 图书馆)、ClinicalTrials.gov、EMBASE 和 Web of Science,检索截至 2018 年 5 月 9 日发表的研究文章。使用 Newcastle-Ottawa 量表评估研究质量。纳入了对患有 IBS 的参与者进行定量粪便微生物群分析的病例对照研究。主要暴露测量指标为每克粪便的细菌计数对数。使用 Revman 5.3 和 R 3.5.1 中的随机效应模型和倒数方差,对 IBS 患者和健康对照组之间的肠道微生物群的平均差异(MD)进行荟萃分析。使用漏斗图和 Egger 检验评估发表偏倚。使用 95%置信区间的 Higgins I 统计量分析研究间异质性。
共确定了 6333 篇独特的文章;52 篇符合全文筛选标准。其中,23 项研究被纳入分析(北美、欧洲和亚洲的 1340 名参与者)。总体而言,这些研究的质量中等。与健康对照组相比,IBS 患者的粪便乳酸杆菌(MD=-0.57 对数菌落形成单位[CFU]/g;P<0.01)和双歧杆菌(MD=-1.04 对数 CFU/g;P<0.01)水平较低,大肠杆菌(MD=0.60 对数 CFU/g;P<0.01)水平较高,肠杆菌(MD=0.74 对数 CFU/g;P=0.05)水平略高。IBS 患者和健康对照组的粪便拟杆菌和肠球菌无差异(P=0.18 和 0.68)。除双歧杆菌(P=0.015)外,未观察到发表偏倚。腹泻为主型和便秘为主型 IBS 患者的亚组分析结果与主要结果一致。对中国研究的亚组分析结果与主要结果一致,除粪便拟杆菌外,IBS 患者的拟杆菌水平高于健康对照组(MD=0.29;95%CI 0.13 至 0.46;P<0.01)。尽管大多数比较中都存在显著的异质性(I>75%),但研究结果的效应估计方向相对一致。
IBS 的特征是肠道微生物失调。需要前瞻性的大规模研究来阐明肠道微生物谱如何用于指导这一具有挑战性的患者群体的靶向治疗。