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

被引:2
|
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.
引用
收藏
页数:14
相关论文
共 50 条
  • [21] Causal effect of gut microbiota on the risk of prostatitis: a two-sample Mendelian randomization study
    Liu, Dalu
    Mei, Yangyang
    Ji, Nuo
    Zhang, Bo
    Feng, Xingliang
    INTERNATIONAL UROLOGY AND NEPHROLOGY, 2024, 56 (09) : 2839 - 2850
  • [22] Exploring the role of gut microbiota in migraine risk: a two-sample Mendelian randomization study
    Meng, Xiangyue
    Li, Quan
    Wang, Delong
    Li, Jinting
    Cui, Yang
    Sun, Zhongren
    Yin, Hongna
    SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2024, 59 (04) : 411 - 418
  • [23] Gut microbiota and risk of iron deficiency anemia: A two-sample Mendelian randomization study
    Lei, Wenhui
    Liu, Zhaoyun
    Lai, Hai-Ping
    Fu, Rong
    MEDICINE, 2025, 104 (08)
  • [24] Gut microbiota and risk of coronary heart disease: a two-sample Mendelian randomization study
    Hu, Xiang-zhi
    Fu, Ling-ling
    Ye, Bin
    Ao, Man
    Yan, Ming
    Feng, Hong-chao
    FRONTIERS IN CARDIOVASCULAR MEDICINE, 2024, 11
  • [25] Causal effects of gut microbiota on the risk of periodontitis: a two-sample Mendelian randomization study
    Luo, Shulu
    Li, Weiran
    Li, Qianqian
    Zhang, Mengqi
    Wang, Xun
    Wu, Shuyi
    Li, Yan
    FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2023, 13
  • [26] Gut microbiota and chronic rhinosinusitis: a two-sample Mendelian randomization study
    Zhang, Fang
    Cai, Boyu
    Luo, Jing
    Xiao, Yixi
    Tian, Yang
    Sun, Yi
    Liu, Huanhai
    Zhang, Jianhui
    EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2024, 281 (06) : 3025 - 3030
  • [27] Gut microbiota and functional dyspepsia: a two-sample Mendelian randomization study
    Xv, Yichuan
    Chen, Jiaxu
    Lin, Jiang
    FRONTIERS IN MICROBIOLOGY, 2024, 15
  • [28] Gut microbiota and male fertility: A two-sample Mendelian randomization study
    Wang, Zhi-hong
    Kang, Yi-fan
    MEDICINE, 2025, 104 (08)
  • [29] Gut microbiota and chronic rhinosinusitis: a two-sample Mendelian randomization study
    Fang Zhang
    Boyu Cai
    Jing Luo
    Yixi Xiao
    Yang Tian
    Yi Sun
    Huanhai Liu
    Jianhui Zhang
    European Archives of Oto-Rhino-Laryngology, 2024, 281 : 3025 - 3030
  • [30] Gut microbiota and atopic dermatitis: a two-sample Mendelian randomization study
    Xue, Yan
    Zhang, Linzhu
    Chen, Yajun
    Wang, Han
    Xie, Jiang
    FRONTIERS IN MEDICINE, 2023, 10