Mendelian randomization suggests a causal relationship between gut microbiota and nonalcoholic fatty liver disease in humans

被引:1
|
作者
Dai, Xiangyi [1 ,2 ]
Jiang, Kaiping [1 ,2 ]
Ma, Xiaojun [1 ,2 ]
Hu, Hongtao [1 ,2 ]
Mo, Xiaoai [1 ,2 ]
Huang, Kaizhou [1 ,2 ]
Jiang, Qunfang [1 ,2 ]
Chen, Ying [1 ,2 ]
Liu, Chonglin [1 ,2 ]
机构
[1] Guangzhou Univ Chinese Med, Clin Coll 8, 6 Qinren Rd, Foshan 528051, Peoples R China
[2] Foshan Hosp Tradit Chinese Med, Dept Hepatol, Foshan, Peoples R China
关键词
genetics; gut microbiota; Mendelian randomization; nonalcoholic fatty liver disease; SNPs;
D O I
10.1097/MD.0000000000037478
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Targeting the gut microbiota is an emerging strategy to treat nonalcoholic fatty liver disease (NAFLD). Nonetheless, the causal relationship between specific gut microbiota and NAFLD remains unclear. We first obtained genome-wide association study statistics on gut microbiota and NAFLD from publicly available databases. We then performed the Mendelian randomization (MR) analysis to determine the potential causal relationship between the gut microbiota and NAFLD by 5 different methods, and conducted a series of sensitivity analyses to validate the robustness of the MR analysis results. Furthermore, we investigated the direction of causality by bidirectional MR analysis. For 211 gut microbiota, 2 MR methods confirmed that phylum Tenericutes, class Deltaproteobacteria and class Mollicutes were significantly associated with the risk of NAFLD. Heterogeneity (P > .05) and pleiotropy (P > .05) analyses validated the robustness of the MR results. There was no causal effect of NAFLD on these bacterial taxa in the reverse MR analysis. We identified specific gut microbiota with causal effects on NAFLD through gene prediction, which may provide useful guidance for targeting the gut microbiota to intervene and treat NAFLD.
引用
收藏
页数:7
相关论文
共 50 条
  • [31] The causal relationship between gut microbiota and immune skin diseases: A bidirectional Mendelian randomization
    Feng, Fei
    Li, Ruicheng
    Tian, Rui
    Wu, Xueyi
    Zhang, Nannan
    Nie, Zhenhua
    PLOS ONE, 2024, 19 (03):
  • [32] Causal associations between gut microbiota and Cholestatic liver diseases: a Mendelian randomization study
    Yang, Jiaqi
    Ma, Gang
    Wang, Kemei
    Yang, Hui
    Jiang, Shuangshuang
    Fan, Qingling
    Zhou, Xinmin
    Guo, Guanya
    Han, Ying
    FRONTIERS IN MEDICINE, 2024, 11
  • [33] Causal relationship between gut microbiota and myasthenia gravis: a bidirectional mendelian randomization study
    Su, Tengfei
    Yin, Xiang
    Ren, Jiaxin
    Lang, Yue
    Zhang, Weiguanliu
    Cui, Li
    CELL AND BIOSCIENCE, 2023, 13 (01):
  • [34] Causal relationship between gut microbiota and male erectile dysfunction: a Mendelian randomization analysis
    Chen, Shuaiqi
    Liu, Xiaolong
    Wu, Shangrong
    Sun, Guangyu
    Liu, Ranlu
    FRONTIERS IN MICROBIOLOGY, 2024, 15
  • [35] Investigating the causal associations between five anthropometric indicators and nonalcoholic fatty liver disease: Mendelian randomization study
    Xiao, Xian-Pei
    Dai, Yong-Jun
    Zhang, Yu
    Yang, Meng
    Xie, Jian
    Chen, Guo
    Yang, Zheng-Jun
    WORLD JOURNAL OF CLINICAL CASES, 2024, 12 (07)
  • [36] Investigating the causal relationship of gut microbiota with GERD and BE: a bidirectional mendelian randomization
    Liu, Yuan
    Yu, Jiali
    Yang, Yuxiao
    Han, Bingyu
    Wang, Qiao
    Du, Shiyu
    BMC GENOMICS, 2024, 25 (01):
  • [37] Causal relationship of gut microbiota with diabetic nephropathy: a Mendelian randomization analysis
    Yan, Wei
    Ge, Ying
    Wang, Lina
    Wang, Yuntao
    He, Daikun
    FRONTIERS IN MICROBIOLOGY, 2024, 14
  • [38] Causal relationship between the gut microbiota, immune cells, and coronary heart disease: a mediated Mendelian randomization analysis
    Yang, Feifei
    Song, Hui
    Tang, Weizhi
    Liu, Lingyun
    Zhu, Ziyi
    Bin, Ouyang
    Zhang, Liwen
    He, Guixin
    Qin, Weibin
    FRONTIERS IN MICROBIOLOGY, 2024, 15
  • [39] Causal association of nonalcoholic fatty liver disease with 22 extrahepatic cancers: A Mendelian randomization study
    Xie, Jiarong
    Gao, Hui
    Liu, Cenqin
    Pan, Yue
    Xu, Chengfu
    Xu, Lei
    HEPATOLOGY RESEARCH, 2024, 54 (03) : 261 - 271
  • [40] Causal effects of female reproductive features on nonalcoholic fatty liver disease: A mendelian randomization study
    Fu, Haoshuang
    Song, Shuying
    Du, Bingying
    Zhou, Tianhui
    Cai, Minghao
    Jiang, Shaowen
    Chen, Yaoxing
    Zang, Xinya
    Huang, Yan
    Wang, Weijing
    Xie, Qing
    JOURNAL OF GENE MEDICINE, 2024, 26 (09):