| Literature DB >> 28494241 |
Ashwin N Ananthakrishnan1, Chengwei Luo2, Vijay Yajnik1, Hamed Khalili1, John J Garber3, Betsy W Stevens4, Thomas Cleland3, Ramnik J Xavier5.
Abstract
The gut microbiome plays a central role in inflammatory bowel diseases (IBDs) pathogenesis and propagation. To determine whether the gut microbiome may predict responses to IBD therapy, we conducted a prospective study with Crohn's disease (CD) or ulcerative colitis (UC) patients initiating anti-integrin therapy (vedolizumab). Disease activity and stool metagenomes at baseline, and weeks 14, 30, and 54 after therapy initiation were assessed. Community α-diversity was significantly higher, and Roseburia inulinivorans and a Burkholderiales species were more abundant at baseline among CD patients achieving week 14 remission. Several significant associations were identified with microbial function; 13 pathways including branched chain amino acid synthesis were significantly enriched in baseline samples from CD patients achieving remission. A neural network algorithm, vedoNet, incorporating microbiome and clinical data, provided highest classifying power for clinical remission. We hypothesize that the trajectory of early microbiome changes may be a marker of response to IBD treatment.Entities:
Keywords: Microbiome; butyrate; remission; roseburia; treatment response; vedolizumab
Mesh:
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Year: 2017 PMID: 28494241 PMCID: PMC5705050 DOI: 10.1016/j.chom.2017.04.010
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023