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Low FODMAP Diet for Functional Gastrointestinal Symptoms in Quiescent Inflammatory Bowel Disease: A Systematic Review of Randomized Controlled Trials

机译:低FODMAP饮食对于静态炎症性肠病中的功能性胃肠道症状:对随机对照试验的系统综述

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摘要

A low FODMAP diet (LFD) has been hypothesized to relieve symptoms of functional gastrointestinal disorders (FGD) in patients with inflammatory bowel disease (IBD). The aim of the study was to systematically review the literature for randomized controlled trials (RCTs) assessing the effectiveness of the LFD in patients with IBD and FGD. Four databases were searched, but a meta-analysis was not performed due to methodological and outcomes heterogeneity. Four RCTs fulfilled the criteria, with three having some concerns in their risk of bias assessment. All interventions compared the LFDs against a “typical” or sham diet, spanning in duration from 21 days to 6 weeks. Quality of life was improved in two RCTs, while revealing inconsistent findings in the third trial, based on different assessment tools. The fecal assays revealed non-significant findings for most variables (fecal weight, pH, water content, gene count, and gut transit time) and inconsistent findings concerning stool frequency and short-chain fatty acids concentration. Levels of fecal calprotectin, CRP, or T-cell phenotype did not differ between intervention and comparator arms. Two RCTs reported a reduction in abdominal pain, while results concerning pain duration and bloating were inconsistent. In one trial, energy intake was considerably reduced among LFD participants. Regarding gut microbiota, no differences were noted. A considerable degree of methodological and outcome heterogeneity was observed, paired with results inconsistency. The available data are not sufficient to justify the claim that an LFD induces relief of FGD symptoms, although it may pave the way to a placebo response.
机译:已经假设低FODMAP饮食(LFD)以缓解炎症性肠病(IBD)患者功能胃肠疾病(FGD)的症状。该研究的目的是系统地审查随机对照试验(RCT)的文献,评估IBD和FGD患者LFD的有效性。搜索四个数据库,但由于方法论和结果异质性而未进行META分析。四个rcts满足了标准,其中三个对其偏见评估风险有一些担忧。所有干预措施将LFD与“典型”或假饮食相比,持续时间为21天至6周。两个RCT的生活质量得到改善,同时基于不同的评估工具,在第三次试验中揭示了不一致的结果。粪便测定显示出大多数变量(粪便重量,pH,水含量,基因计数和肠道转运时间)和肠频率和短链脂肪酸浓度的不一致结果。粪便酸蛋白,CRP或T细胞表型的水平在干预和比较器臂之间没有区别。两个RCT报告腹痛减少,同时有关疼痛持续时间和膨胀的结果是不一致的。在一次试验中,LFD参与者的能量摄入量显着减少。关于肠道微生物群,没有注意到没有差异。观察到相当程度的方法和结果异质性,与结果不一致配对。可用数据不足以证明LFD诱导FGD症状的缓解,尽管它可能会铺平到安慰剂响应。

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