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Microbial Associations With Microscopic Colitis

Microscopic colitis is a relatively common cause of chronic diarrhea and may be linked to luminal factors. Given the essential role of the microbiome in human gut health, analysis of microbiome changes associated with microscopic colitis could provide insights into the development of the disease. ME...

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Autores principales: Sun, Shan, Blakley, Ivory C., Fodor, Anthony A., Keku, Temitope O., Woosley, John T., Peery, Anne F., Sandler, Robert S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624492/
https://www.ncbi.nlm.nih.gov/pubmed/36094869
http://dx.doi.org/10.14309/ctg.0000000000000528
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author Sun, Shan
Blakley, Ivory C.
Fodor, Anthony A.
Keku, Temitope O.
Woosley, John T.
Peery, Anne F.
Sandler, Robert S.
author_facet Sun, Shan
Blakley, Ivory C.
Fodor, Anthony A.
Keku, Temitope O.
Woosley, John T.
Peery, Anne F.
Sandler, Robert S.
author_sort Sun, Shan
collection PubMed
description Microscopic colitis is a relatively common cause of chronic diarrhea and may be linked to luminal factors. Given the essential role of the microbiome in human gut health, analysis of microbiome changes associated with microscopic colitis could provide insights into the development of the disease. METHODS: We enrolled patients who underwent colonoscopy for diarrhea. An experienced pathologist classified patients as having microscopic colitis (n = 52) or controls (n = 153). Research biopsies were taken from the ascending (ASC) and descending (DES) colon, and the microbiome was characterized with Illumina sequencing. We analyzed the associations between microscopic colitis and microbiome with a series of increasingly complex models adjusted for a range of demographic and health factors. RESULTS: We found that alpha diversity was significantly lower in cases with microscopic colitis compared with that in controls in the DES colon microbiome. In the DES colon, a series of models that adjusted for an increasing number of covariates found taxa significantly associated with microscopic colitis, including Proteobacteria that was enriched in cases and Collinsella that was enriched in controls. While the alpha diversity and taxa were not significantly associated with microscopic colitis in the ASC colon microbiome, the inference P values based on ASC and DES microbiomes were highly correlated. DISCUSSION: Our study demonstrates an altered microbiome in cases with microscopic colitis compared with that in controls. Because both the cases and controls experienced diarrhea, we have identified candidate taxa that could be mechanistically responsible for the development of microscopic colitis independent of changes to the microbial community caused by diarrhea.
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spelling pubmed-96244922022-11-03 Microbial Associations With Microscopic Colitis Sun, Shan Blakley, Ivory C. Fodor, Anthony A. Keku, Temitope O. Woosley, John T. Peery, Anne F. Sandler, Robert S. Clin Transl Gastroenterol Article Microscopic colitis is a relatively common cause of chronic diarrhea and may be linked to luminal factors. Given the essential role of the microbiome in human gut health, analysis of microbiome changes associated with microscopic colitis could provide insights into the development of the disease. METHODS: We enrolled patients who underwent colonoscopy for diarrhea. An experienced pathologist classified patients as having microscopic colitis (n = 52) or controls (n = 153). Research biopsies were taken from the ascending (ASC) and descending (DES) colon, and the microbiome was characterized with Illumina sequencing. We analyzed the associations between microscopic colitis and microbiome with a series of increasingly complex models adjusted for a range of demographic and health factors. RESULTS: We found that alpha diversity was significantly lower in cases with microscopic colitis compared with that in controls in the DES colon microbiome. In the DES colon, a series of models that adjusted for an increasing number of covariates found taxa significantly associated with microscopic colitis, including Proteobacteria that was enriched in cases and Collinsella that was enriched in controls. While the alpha diversity and taxa were not significantly associated with microscopic colitis in the ASC colon microbiome, the inference P values based on ASC and DES microbiomes were highly correlated. DISCUSSION: Our study demonstrates an altered microbiome in cases with microscopic colitis compared with that in controls. Because both the cases and controls experienced diarrhea, we have identified candidate taxa that could be mechanistically responsible for the development of microscopic colitis independent of changes to the microbial community caused by diarrhea. Wolters Kluwer 2022-08-27 /pmc/articles/PMC9624492/ /pubmed/36094869 http://dx.doi.org/10.14309/ctg.0000000000000528 Text en © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Article
Sun, Shan
Blakley, Ivory C.
Fodor, Anthony A.
Keku, Temitope O.
Woosley, John T.
Peery, Anne F.
Sandler, Robert S.
Microbial Associations With Microscopic Colitis
title Microbial Associations With Microscopic Colitis
title_full Microbial Associations With Microscopic Colitis
title_fullStr Microbial Associations With Microscopic Colitis
title_full_unstemmed Microbial Associations With Microscopic Colitis
title_short Microbial Associations With Microscopic Colitis
title_sort microbial associations with microscopic colitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624492/
https://www.ncbi.nlm.nih.gov/pubmed/36094869
http://dx.doi.org/10.14309/ctg.0000000000000528
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