Comprehensive cross-cohort analysis reveals global gut microbiome signatures of celiac disease.

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Peter J Prendergast, Haig V Bishop, Craig W Herbold, Elena F Verdu, Renwick C J Dobson, Andrew S Day, Olivia J Ogilvie
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Abstract

Background: Celiac disease affects ~1-2% of people and remains incurable, requiring lifelong dietary restriction. The gut microbiome is thought to contribute to the development and progression of celiac disease. However, findings across previous studies are fragmented, making it difficult to understand exactly how the gut microbiome is involved.

Methods: We integrate over 900 samples from global datasets spanning different disease stages (before onset, during active disease, and after treatment), body sites, and research methods. Datasets produced using both 16S rRNA gene sequencing and shotgun metagenomics profile the gut microbiome. Alpha and beta diversity analyses and differential abundance testing identify consistent changes in bacterial communities linked to celiac disease. Machine learning tests how well microbiome data predicts disease status.

Results: Here, we show that celiac disease is not marked by large changes in gut microbiome diversity. Instead, there are subtle, consistent changes in specific bacteria, including a reduction in beneficial butyrate producers (Faecalibacterium, Prevotella, Agathobacter, Gemmiger), changes in mucin-associated microbes (Akkermansia muciniphila), and an increase in potentially harmful bacteria (Helicobacter, Campylobacter, Haemophilus parainfluenzae). These changes are seen before and during active disease and persist on a gluten-free diet. Microbiome-based disease prediction is moderately accurate for active disease and weaker for prospective performance, likely constrained by training data.

Conclusions: Our findings suggest that celiac disease is linked to specific changes in gut bacteria that are not fully resolved by diet alone. Future treatments may need to focus on restoring healthy gut bacteria, not just avoiding gluten, to better manage the disease.

全面的跨队列分析揭示了乳糜泻的全球肠道微生物组特征。
背景:乳糜泻影响约1-2%的人,并且仍然无法治愈,需要终生限制饮食。肠道微生物群被认为与乳糜泻的发生和发展有关。然而,之前的研究结果是零散的,因此很难确切地理解肠道微生物群是如何参与的。方法:我们整合了来自全球不同疾病阶段(发病前、活动性疾病期间和治疗后)、身体部位和研究方法的900多个样本。使用16S rRNA基因测序和霰弹枪宏基因组学产生的数据集描述了肠道微生物组。α和β多样性分析和差异丰度测试确定了与乳糜泻相关的细菌群落的一致变化。机器学习测试微生物组数据预测疾病状态的效果。结果:在这里,我们发现乳糜泻并不以肠道微生物群多样性的大变化为特征。相反,在特定细菌中存在细微的、一致的变化,包括有益的丁酸盐产生菌(粪杆菌、普雷沃氏菌、Agathobacter、Gemmiger)减少,黏液蛋白相关微生物(嗜黏液杆菌)的变化,以及潜在有害细菌(幽门螺杆菌、弯曲杆菌、副流感嗜血杆菌)的增加。这些变化在活动性疾病之前和期间都可以看到,并且在无麸质饮食中持续存在。基于微生物组的疾病预测对活动性疾病的准确性中等,对前瞻性表现的准确性较弱,可能受到训练数据的限制。结论:我们的研究结果表明,乳糜泻与肠道细菌的特定变化有关,而这种变化仅靠饮食是无法完全解决的。未来的治疗可能需要专注于恢复健康的肠道细菌,而不仅仅是避免麸质,以更好地控制疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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