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Gut microbiota and common gastrointestinal diseases: a bidirectional two-sample Mendelian randomized study

BACKGROUND: Several recent studies have shown an association between gut microbiota and gastrointestinal diseases. However, the causal relationship between gut microbiota and gastrointestinal disorders is unclear. METHODS: We assessed causal relationships between gut microbiota and eight common gast...

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Autores principales: Qiu, Binxu, Shen, Zixiong, Yang, Dongliang, Qin, Xinxin, Ren, Wenyong, Wang, Quan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10691374/
https://www.ncbi.nlm.nih.gov/pubmed/38045030
http://dx.doi.org/10.3389/fmicb.2023.1273269
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author Qiu, Binxu
Shen, Zixiong
Yang, Dongliang
Qin, Xinxin
Ren, Wenyong
Wang, Quan
author_facet Qiu, Binxu
Shen, Zixiong
Yang, Dongliang
Qin, Xinxin
Ren, Wenyong
Wang, Quan
author_sort Qiu, Binxu
collection PubMed
description BACKGROUND: Several recent studies have shown an association between gut microbiota and gastrointestinal diseases. However, the causal relationship between gut microbiota and gastrointestinal disorders is unclear. METHODS: We assessed causal relationships between gut microbiota and eight common gastrointestinal diseases using Mendelian randomization (MR) analyses. IVW results were considered primary results. Cochrane’s Q and MR-Egger tests were used to test for heterogeneity and pleiotropy. Leave-one-out was used to test the stability of the MR results, and Bonferroni correction was used to test the strength of the causal relationship between exposure and outcome. RESULTS: MR analyses of 196 gut microbiota and eight common gastrointestinal disease phenotypes showed 62 flora and common gastrointestinal diseases with potential causal relationships. Among these potential causal relationships, after the Bonferroni-corrected test, significant causal relationships remained between Genus Oxalobacter and CD (OR = 1.29, 95% CI: 1.13–1.48, p = 2.5 × 10–4, q = 4.20 × 10–4), and between Family Clostridiaceae1 and IBS (OR = 0.9967, 95% CI: 0.9944–0.9991, p = 1.3 × 10–3, q = 1.56 × 10–3). Cochrane’s Q-test showed no significant heterogeneity among the various single nucleotide polymorphisms (SNPs). In addition, no significant level of pleiotropy was found according to the MR-Egger. CONCLUSION: This study provides new insights into the mechanisms of gut microbiota-mediated gastrointestinal disorders and some guidance for targeting specific gut microbiota for treating gastrointestinal disorders.
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spelling pubmed-106913742023-12-02 Gut microbiota and common gastrointestinal diseases: a bidirectional two-sample Mendelian randomized study Qiu, Binxu Shen, Zixiong Yang, Dongliang Qin, Xinxin Ren, Wenyong Wang, Quan Front Microbiol Microbiology BACKGROUND: Several recent studies have shown an association between gut microbiota and gastrointestinal diseases. However, the causal relationship between gut microbiota and gastrointestinal disorders is unclear. METHODS: We assessed causal relationships between gut microbiota and eight common gastrointestinal diseases using Mendelian randomization (MR) analyses. IVW results were considered primary results. Cochrane’s Q and MR-Egger tests were used to test for heterogeneity and pleiotropy. Leave-one-out was used to test the stability of the MR results, and Bonferroni correction was used to test the strength of the causal relationship between exposure and outcome. RESULTS: MR analyses of 196 gut microbiota and eight common gastrointestinal disease phenotypes showed 62 flora and common gastrointestinal diseases with potential causal relationships. Among these potential causal relationships, after the Bonferroni-corrected test, significant causal relationships remained between Genus Oxalobacter and CD (OR = 1.29, 95% CI: 1.13–1.48, p = 2.5 × 10–4, q = 4.20 × 10–4), and between Family Clostridiaceae1 and IBS (OR = 0.9967, 95% CI: 0.9944–0.9991, p = 1.3 × 10–3, q = 1.56 × 10–3). Cochrane’s Q-test showed no significant heterogeneity among the various single nucleotide polymorphisms (SNPs). In addition, no significant level of pleiotropy was found according to the MR-Egger. CONCLUSION: This study provides new insights into the mechanisms of gut microbiota-mediated gastrointestinal disorders and some guidance for targeting specific gut microbiota for treating gastrointestinal disorders. Frontiers Media S.A. 2023-11-17 /pmc/articles/PMC10691374/ /pubmed/38045030 http://dx.doi.org/10.3389/fmicb.2023.1273269 Text en Copyright © 2023 Qiu, Shen, Yang, Qin, Ren and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Qiu, Binxu
Shen, Zixiong
Yang, Dongliang
Qin, Xinxin
Ren, Wenyong
Wang, Quan
Gut microbiota and common gastrointestinal diseases: a bidirectional two-sample Mendelian randomized study
title Gut microbiota and common gastrointestinal diseases: a bidirectional two-sample Mendelian randomized study
title_full Gut microbiota and common gastrointestinal diseases: a bidirectional two-sample Mendelian randomized study
title_fullStr Gut microbiota and common gastrointestinal diseases: a bidirectional two-sample Mendelian randomized study
title_full_unstemmed Gut microbiota and common gastrointestinal diseases: a bidirectional two-sample Mendelian randomized study
title_short Gut microbiota and common gastrointestinal diseases: a bidirectional two-sample Mendelian randomized study
title_sort gut microbiota and common gastrointestinal diseases: a bidirectional two-sample mendelian randomized study
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10691374/
https://www.ncbi.nlm.nih.gov/pubmed/38045030
http://dx.doi.org/10.3389/fmicb.2023.1273269
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