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

被引:11
|
作者
Shi, Hanyu [1 ]
Zhao, Tong [1 ]
Geng, RuiHui [1 ]
Sun, Liang [2 ]
Fan, Haojun [3 ]
机构
[1] Hosp First Mobile Corps Chinese Peoples Armed Poli, Dept Internal Med, Dingzhou, Hebei, Peoples R China
[2] Characterist Med Ctr Chinese Peoples Armed Police, Dept Pulm & Crit Care, Tianjin, Peoples R China
[3] Tianjin Univ, Inst Disaster & Emergency Med, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
gut microbiota; Mendelian randomization analaysis; chronic respiratory diseases; chronic obstructive pulmonary disease; asthma; idiopathic pulmonary fibrosis; sarcoidosis; pneumoconiosis;
D O I
10.3389/fmicb.2023.1200937
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
IntroductionGrowing 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. MethodsWe 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. ResultsBased 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. DiscussionThis work implies causal relationships between the gut microbiota and CRDs, thereby shedding new light on the gut microbiota-mediated prevention of CRDs.
引用
收藏
页数:14
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