Abstract
AbstractPrior studies indicate no correlation between gut microbiota of healthy first-degree relatives (HFDRs) of Crohn’s disease (CD) patients and development of CD. Here, we utilized HFDRs as controls to examine the microbiota and metabolome in individuals with active (CD-A) and quiescent (CD-R) CD, thereby minimizing the influence of genetic and environmental factors. Compared to non-relative controls, the use of HFDR controls identified fewer differential taxa.Faecalibacterium, Dorea,andFusicatenibactershowed decreased abundances in CD-R, independent of inflammation, and correlated with fecal SCFAs. Validation with a large multi-center cohort confirmed decreased abundances inFaecalibacteriumand other SCFA-producing genera in CD-R. Classification models based on these genera distinguished CD-R and CD-A from healthy individuals, in both the discovery and validation cohorts. Thus, the decreased presence ofFaecalibacterium, Dorea,andFusicatenibacterin CD-R likely contributed to disease relapse through reduced SCFA production, highlighting their potential as diagnostic markers and therapeutic targets for CD.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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