Literature DB >> 30308161

Compositional and Temporal Changes in the Gut Microbiome of Pediatric Ulcerative Colitis Patients Are Linked to Disease Course.

Melanie Schirmer1, Lee Denson2, Hera Vlamakis3, Eric A Franzosa1, Sonia Thomas4, Nathan M Gotman5, Paul Rufo6, Susan S Baker7, Cary Sauer8, James Markowitz9, Marian Pfefferkorn10, Maria Oliva-Hemker11, Joel Rosh12, Anthony Otley13, Brendan Boyle14, David Mack15, Robert Baldassano16, David Keljo17, Neal LeLeiko18, Melvin Heyman19, Anne Griffiths20, Ashish S Patel21, Joshua Noe22, Subra Kugathasan8, Thomas Walters20, Curtis Huttenhower1, Jeffrey Hyams23, Ramnik J Xavier24.   

Abstract

Evaluating progression risk and determining optimal therapy for ulcerative colitis (UC) is challenging as many patients exhibit incomplete responses to treatment. As part of the PROTECT (Predicting Response to Standardized Colitis Therapy) Study, we evaluated the role of the gut microbiome in disease course for 405 pediatric, new-onset, treatment-naive UC patients. Patients were monitored for 1 year upon treatment initiation, and microbial taxonomic composition was analyzed from fecal samples and rectal biopsies. Depletion of core gut microbes and expansion of bacteria typical of the oral cavity were associated with baseline disease severity. Remission and refractory disease were linked to species-specific temporal changes that may be implicative of therapy efficacy, and a pronounced increase in microbiome variability was observed prior to colectomy. Finally, microbial associations with disease-associated serological markers suggest host-microbial interactions in UC. These insights will help improve existing treatments and develop therapeutic approaches guiding optimal medical care.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  5ASA; colectomy; corticosteroids; disease course; gut microbiome; host-microbial interactions; pediatric ulcerative colitis; response to therapy; serological markers; treatment-naive

Mesh:

Substances:

Year:  2018        PMID: 30308161      PMCID: PMC6277984          DOI: 10.1016/j.chom.2018.09.009

Source DB:  PubMed          Journal:  Cell Host Microbe        ISSN: 1931-3128            Impact factor:   21.023


  49 in total

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