Gut microbiota and risk of lower respiratory tract infections: a bidirectional two-sample Mendelian randomization study

被引:1
|
作者
Liu, Wei [1 ]
Wang, Xinyan [1 ]
Feng, Ruizhi [1 ]
Zhao, Chen [2 ,3 ]
Luo, Jian [4 ,5 ]
Zhang, Xiawei [4 ,5 ]
Liu, Xuemei [1 ,6 ]
Yang, Mei [1 ]
Min, Jie [1 ]
Mao, Bing [1 ]
Jiang, Hongli [1 ]
机构
[1] Sichuan Univ, West China Hosp, Inst Integrated Tradit Chinese & Western Med, Div Pulm Med,Dept Internal Med, Chengdu, Peoples R China
[2] Stomatol Hosp, Shanghai Engn Res Ctr Tooth Restorat & Regenerat, Dept Oral Med, Shanghai, Peoples R China
[3] Tongji Univ, Dent Sch, Shanghai, Peoples R China
[4] Univ Oxford, Oxford Biomed Res Ctr, Resp Med Unit, Oxford, England
[5] Univ Oxford, Oxford Biomed Res Ctr, Nuffield Dept Med Expt Med, Natl Inst Hlth Res, Oxford, England
[6] Sichuan Univ, West China Hosp, Dept Pulm Dis, State Key Lab Biotherapy China, Chengdu, Peoples R China
关键词
gut microbiota; lower respiratory tract infections; causal relationship; Mendelian randomization; Blautia genus; INSTRUMENTAL VARIABLES; EARLY-LIFE; BIFIDOBACTERIUM; INFLAMMATION; PROBIOTICS; HEALTH; PREVENTION; MANAGEMENT; DEFENSE;
D O I
10.3389/fmicb.2023.1276046
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Introduction: Observational studies have reported the association between gut microbiota and the risk of lower respiratory tract infections (LRTIs). However, whether the association reflects a causal relationship remains obscure.Methods: A bidirectional twosample Mendelian randomization (MR) analysis was conducted by assessing genome-wide association study (GWAS) summary statistics for gut microbiota taxa and five common LRTIs. MR methods including inverse-variance-weighted (IVW), MR-Egger, weighted median, simple mode, and weighted mode were used to analyze the causality. Gene pleiotropy was tested using MR-Egger regression and MR-PRESSO methods. Cochran's Q test was used to check for heterogeneity. Leave-one-out analysis was used to assess the stability of effect sizes. Detected significant associations were validated by using an independent LRTI GWAS summary statistics dataset. An optional MR method of causal analysis using summary effect estimates (CAUSE) was further performed as a validation to avoid potential false-positive results.Results: According to the MR-Egger estimates in forward MR analysis, a causal effect of gut Blautia on increased odds of bronchiectasis and pneumonia was suggested. MR-Egger regression pleiotropy intercept methods detected no significant horizontal pleiotropy between the instrumental variables of these associations. MR-PRESSO global test examined no potential horizontal pleiotropy. Cochran's Q test showed that no heterogeneity biased the results. The leave-one-out sensitivity analyses suggested robust causality results. These associations with consistent effect direction were successfully replicated in IVW analysis by using the validation GWAS dataset. However, these evidence of causality did not survive after applying strict Bonferroni correction or CAUSE analysis. The reverse MR analysis failed to achieve consistent results in the effect of LRTIs on gut microbiota through comprehensive discovery and validation processes.Discussion: This study established no strong causality between genetically predicted gut microbiome and the risk of lower respiratory tract infections. However, specific subtypes of microbial genera, such as Blautia, were identified as potential influencers and require further investigation, particularly at the species or strain levels.
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页数:14
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