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Mucosa-associated gut microbiota reflects clinical course of ulcerative colitis

This longitudinal study was designed to elucidate whether gut microbiota is associated with relapse and treatment response in ulcerative colitis (UC) patients. Fifty-one patients with UC were enrolled between 2012 and 2017, and followed up through 2020. Colon mucosal biopsy were obtained at enrollme...

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Autores principales: Nishihara, Yuichiro, Ogino, Haruei, Tanaka, Masaru, Ihara, Eikichi, Fukaura, Keita, Nishioka, Kei, Chinen, Takatoshi, Tanaka, Yoshimasa, Nakayama, Jiro, Kang, Dongchon, Ogawa, Yoshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253849/
https://www.ncbi.nlm.nih.gov/pubmed/34215773
http://dx.doi.org/10.1038/s41598-021-92870-0
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author Nishihara, Yuichiro
Ogino, Haruei
Tanaka, Masaru
Ihara, Eikichi
Fukaura, Keita
Nishioka, Kei
Chinen, Takatoshi
Tanaka, Yoshimasa
Nakayama, Jiro
Kang, Dongchon
Ogawa, Yoshihiro
author_facet Nishihara, Yuichiro
Ogino, Haruei
Tanaka, Masaru
Ihara, Eikichi
Fukaura, Keita
Nishioka, Kei
Chinen, Takatoshi
Tanaka, Yoshimasa
Nakayama, Jiro
Kang, Dongchon
Ogawa, Yoshihiro
author_sort Nishihara, Yuichiro
collection PubMed
description This longitudinal study was designed to elucidate whether gut microbiota is associated with relapse and treatment response in ulcerative colitis (UC) patients. Fifty-one patients with UC were enrolled between 2012 and 2017, and followed up through 2020. Colon mucosal biopsy were obtained at enrollment, and 16S ribosomal RNA sequencing was performed using extracted RNA. Of the 51 patients, 24 were in remission and 27 had active UC at enrollment. Of the 24 patients in remission, 17 maintained remission and 7 developed relapse during follow-up. The 7 patients with relapse showed lower diversity, with a lower proportion of Clostridiales (p = 0.0043), and a higher proportion of Bacteroides (p = 0.047) at enrollment than those without relapse. The 27 patients with active UC were classified into response (n = 6), refractory (n = 13), and non-response (n = 8) groups according to their treatment response in 6 months. The refractory and non-response groups showed lower diversity with a lower proportion of Prevotella (p = 0.048 and 0.043) at enrollment than the response group. This study is the first demonstration that reduced diversity and particular microbes are associated with the later clinical course of relapse events and treatment response in UC.
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spelling pubmed-82538492021-07-06 Mucosa-associated gut microbiota reflects clinical course of ulcerative colitis Nishihara, Yuichiro Ogino, Haruei Tanaka, Masaru Ihara, Eikichi Fukaura, Keita Nishioka, Kei Chinen, Takatoshi Tanaka, Yoshimasa Nakayama, Jiro Kang, Dongchon Ogawa, Yoshihiro Sci Rep Article This longitudinal study was designed to elucidate whether gut microbiota is associated with relapse and treatment response in ulcerative colitis (UC) patients. Fifty-one patients with UC were enrolled between 2012 and 2017, and followed up through 2020. Colon mucosal biopsy were obtained at enrollment, and 16S ribosomal RNA sequencing was performed using extracted RNA. Of the 51 patients, 24 were in remission and 27 had active UC at enrollment. Of the 24 patients in remission, 17 maintained remission and 7 developed relapse during follow-up. The 7 patients with relapse showed lower diversity, with a lower proportion of Clostridiales (p = 0.0043), and a higher proportion of Bacteroides (p = 0.047) at enrollment than those without relapse. The 27 patients with active UC were classified into response (n = 6), refractory (n = 13), and non-response (n = 8) groups according to their treatment response in 6 months. The refractory and non-response groups showed lower diversity with a lower proportion of Prevotella (p = 0.048 and 0.043) at enrollment than the response group. This study is the first demonstration that reduced diversity and particular microbes are associated with the later clinical course of relapse events and treatment response in UC. Nature Publishing Group UK 2021-07-02 /pmc/articles/PMC8253849/ /pubmed/34215773 http://dx.doi.org/10.1038/s41598-021-92870-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Nishihara, Yuichiro
Ogino, Haruei
Tanaka, Masaru
Ihara, Eikichi
Fukaura, Keita
Nishioka, Kei
Chinen, Takatoshi
Tanaka, Yoshimasa
Nakayama, Jiro
Kang, Dongchon
Ogawa, Yoshihiro
Mucosa-associated gut microbiota reflects clinical course of ulcerative colitis
title Mucosa-associated gut microbiota reflects clinical course of ulcerative colitis
title_full Mucosa-associated gut microbiota reflects clinical course of ulcerative colitis
title_fullStr Mucosa-associated gut microbiota reflects clinical course of ulcerative colitis
title_full_unstemmed Mucosa-associated gut microbiota reflects clinical course of ulcerative colitis
title_short Mucosa-associated gut microbiota reflects clinical course of ulcerative colitis
title_sort mucosa-associated gut microbiota reflects clinical course of ulcerative colitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253849/
https://www.ncbi.nlm.nih.gov/pubmed/34215773
http://dx.doi.org/10.1038/s41598-021-92870-0
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