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The associations between gut microbiota and chronic respiratory diseases: a Mendelian randomization study

INTRODUCTION: Growing evidence indicates that variations in the composition of the gut microbiota are linked to the onset and progression of chronic respiratory diseases (CRDs), albeit the causal relationship between the two remains unclear. METHODS: We conducted a comprehensive two-sample Mendelian...

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Autores principales: Shi, Hanyu, Zhao, Tong, Geng, RuiHui, Sun, Liang, Fan, Haojun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272395/
https://www.ncbi.nlm.nih.gov/pubmed/37333634
http://dx.doi.org/10.3389/fmicb.2023.1200937
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author Shi, Hanyu
Zhao, Tong
Geng, RuiHui
Sun, Liang
Fan, Haojun
author_facet Shi, Hanyu
Zhao, Tong
Geng, RuiHui
Sun, Liang
Fan, Haojun
author_sort Shi, Hanyu
collection PubMed
description INTRODUCTION: Growing evidence indicates that variations in the composition of the gut microbiota are linked to the onset and progression of chronic respiratory diseases (CRDs), albeit the causal relationship between the two remains unclear. METHODS: We conducted a comprehensive two-sample Mendelian randomization (MR) analysis to investigate the relationship between gut microbiota and five main CRDs, including chronic obstructive pulmonary disease (COPD), asthma, idiopathic pulmonary fibrosis (IPF), sarcoidosis, and pneumoconiosis. For MR analysis, the inverse variance weighted (IVW) method was utilized as the primary method. The MR–Egger, weighted median, and MR-PRESSO statistical methods were used as a supplement. To detect heterogeneity and pleiotropy, the Cochrane and Rucker Q test, MR–Egger intercept test, and MR-PRESSO global test were then implemented. The leave-one-out strategy was also applied to assess the consistency of the MR results. RESULTS: Based on substantial genetic data obtained from genome-wide association studies (GWAS) comprising 3,504,473 European participants, our study offers evidence that several gut microbial taxa, including 14 probable microbial taxa (specifically, 5, 3, 2, 3 and 1 for COPD, asthma, IPF, sarcoidosis, and pneumoconiosis, respectively) and 33 possible microbial taxa (specifically, 6, 7, 8, 7 and 5 for COPD, asthma, IPF, sarcoidosis, and pneumoconiosis, respectively) play significant roles in the formation of CRDs. DISCUSSION: This work implies causal relationships between the gut microbiota and CRDs, thereby shedding new light on the gut microbiota-mediated prevention of CRDs.
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spelling pubmed-102723952023-06-17 The associations between gut microbiota and chronic respiratory diseases: a Mendelian randomization study Shi, Hanyu Zhao, Tong Geng, RuiHui Sun, Liang Fan, Haojun Front Microbiol Microbiology INTRODUCTION: Growing evidence indicates that variations in the composition of the gut microbiota are linked to the onset and progression of chronic respiratory diseases (CRDs), albeit the causal relationship between the two remains unclear. METHODS: We conducted a comprehensive two-sample Mendelian randomization (MR) analysis to investigate the relationship between gut microbiota and five main CRDs, including chronic obstructive pulmonary disease (COPD), asthma, idiopathic pulmonary fibrosis (IPF), sarcoidosis, and pneumoconiosis. For MR analysis, the inverse variance weighted (IVW) method was utilized as the primary method. The MR–Egger, weighted median, and MR-PRESSO statistical methods were used as a supplement. To detect heterogeneity and pleiotropy, the Cochrane and Rucker Q test, MR–Egger intercept test, and MR-PRESSO global test were then implemented. The leave-one-out strategy was also applied to assess the consistency of the MR results. RESULTS: Based on substantial genetic data obtained from genome-wide association studies (GWAS) comprising 3,504,473 European participants, our study offers evidence that several gut microbial taxa, including 14 probable microbial taxa (specifically, 5, 3, 2, 3 and 1 for COPD, asthma, IPF, sarcoidosis, and pneumoconiosis, respectively) and 33 possible microbial taxa (specifically, 6, 7, 8, 7 and 5 for COPD, asthma, IPF, sarcoidosis, and pneumoconiosis, respectively) play significant roles in the formation of CRDs. DISCUSSION: This work implies causal relationships between the gut microbiota and CRDs, thereby shedding new light on the gut microbiota-mediated prevention of CRDs. Frontiers Media S.A. 2023-06-02 /pmc/articles/PMC10272395/ /pubmed/37333634 http://dx.doi.org/10.3389/fmicb.2023.1200937 Text en Copyright © 2023 Shi, Zhao, Geng, Sun and Fan. 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
Shi, Hanyu
Zhao, Tong
Geng, RuiHui
Sun, Liang
Fan, Haojun
The associations between gut microbiota and chronic respiratory diseases: a Mendelian randomization study
title The associations between gut microbiota and chronic respiratory diseases: a Mendelian randomization study
title_full The associations between gut microbiota and chronic respiratory diseases: a Mendelian randomization study
title_fullStr The associations between gut microbiota and chronic respiratory diseases: a Mendelian randomization study
title_full_unstemmed The associations between gut microbiota and chronic respiratory diseases: a Mendelian randomization study
title_short The associations between gut microbiota and chronic respiratory diseases: a Mendelian randomization study
title_sort associations between gut microbiota and chronic respiratory diseases: a mendelian randomization study
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272395/
https://www.ncbi.nlm.nih.gov/pubmed/37333634
http://dx.doi.org/10.3389/fmicb.2023.1200937
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