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Gut Microbiome Function Predicts Response to Anti-integrin Biologic Therapy in Inflammatory Bowel Diseases.

Ashwin N Ananthakrishnan, Chengwei Luo, Vijay Yajnik, Hamed Khalili, John J Garber et al.
Other Cell host & microbe 2017 399 citations
PubMed DOI
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Study Design

Type d'étude
Observational Study
Population
CD or UC patients starting vedolizumab
Intervention
Gut Microbiome Function Predicts Response to Anti-integrin Biologic Therapy in Inflammatory Bowel Diseases. None
Comparateur
None
Critère de jugement principal
Week 14 remission prediction by microbiome
Direction de l'effet
Mixed
Risque de biais
Moderate

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.

En bref

It is hypothesized that the trajectory of early microbiome changes may be a marker of response to IBD treatment, and a neural network algorithm, vedoNet, incorporating microbiome and clinical data, provided highest classifying power for clinical remission.

Used In Evidence Reviews

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