The associations between modifiable risk factors and nonalcoholic fatty liver disease: A comprehensive Mendelian randomization study

被引:153
作者
Xie, Jiarong [1 ,2 ,3 ]
Huang, Hangkai [1 ]
Liu, Zhening [1 ]
Li, Youming [1 ,3 ]
Yu, Chaohui [1 ,3 ]
Xu, Lei [1 ,2 ,3 ]
Xu, Chengfu [1 ,3 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 1, Dept Gastroenterol, Sch Med, 79 Qingchun Rd, Hangzhou 310003, Peoples R China
[2] Ningbo First Hosp, Dept Gastroenterol, 59 Liuting St, Ningbo 315000, Peoples R China
[3] Zhejiang Prov Clin Res Ctr Digest Dis, Hangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
STEATOHEPATITIS; CONSUMPTION; BIAS;
D O I
10.1002/hep.32728
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims Early identification of modifiable risk factors is essential for the prevention of nonalcoholic fatty liver disease (NAFLD). We aimed to systematically explore the relationships between genetically predicted modifiable risk factors and NAFLD. Approach and Results We applied univariable and multivariable Mendelian randomization analyses to explore the relationships between 35 modifiable risk factors and NAFLD. We also evaluated the combined results in three independent large genome-wide association studies. Genetically predicted alcohol frequency, elevated serum levels of liver enzymes, triglycerides, C-reactive protein, and obesity traits, including body mass index, waist circumference, and body fat mass, were associated with increased risks of NAFLD (all with p < 0.05). Poor physical condition had a suggestive increased risk for NAFLD (odds ratio [OR] = 2.63, p = 0.042). Genetically instrumented type 2 diabetes (T2DM), hypothyroidism, and hypertension all increased the risk for NAFLD, and the ORs (95% confidence interval) were 1.508 (1.20-1.90), 13.08 (1.53-111.65), and 3.11 (1.33-7.31) for a 1-U increase in log-transformed odds, respectively. The positive associations of T2DM and hypertension with NAFLD remained significant in multivariable analyses. The combined results from the discovery and two replication datasets further confirmed that alcohol frequency, elevated serum liver enzymes, poor physical condition, obesity traits, T2DM, and hypertension significantly increase the risk of NAFLD, whereas higher education and high-density lipoprotein cholesterol (HDL-cholesterol) could lower NAFLD risk. Conclusions Genetically predicted alcohol frequency, elevated serum liver enzymes, poor physical condition, obesity traits, T2DM, and hypertension were associated with an increased risk of NAFLD, whereas higher education and HDL-cholesterol were associated with a decreased risk of NAFLD.
引用
收藏
页码:949 / 964
页数:16
相关论文
共 53 条
[1]   Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically characterised cohort [J].
Anstee, Quentin M. ;
Darlay, Rebecca ;
Cockell, Simon ;
Meroni, Marica ;
Govaere, Olivier ;
Tiniakos, Dina ;
Burt, Alastair D. ;
Bedossa, Pierre ;
Palmer, Jeremy ;
Liu, Yang-Lin ;
Aithal, Guruprasad P. ;
Allison, Michael ;
Yki-Jarvinen, Hannele ;
Vacca, Michele ;
Dufour, Jean-Francois ;
Invernizzi, Pietro ;
Prati, Daniele ;
Ekstedt, Mattias ;
Kechagias, Stergios ;
Francque, Sven ;
Petta, Salvatore ;
Bugianesi, Elisabetta ;
Clement, Karine ;
Ratziu, Vlad ;
Schattenberg, Joern M. ;
Valenti, Luca ;
Day, Christopher P. ;
Cordell, Heather J. ;
Daly, Ann K. .
JOURNAL OF HEPATOLOGY, 2020, 73 (03) :505-515
[2]   A framework for the investigation of pleiotropy in two-sample summary data Mendelian randomization [J].
Bowden, Jack ;
Del Greco, Fabiola M. ;
Minelli, Cosetta ;
Smith, George Davey ;
Sheehan, Nuala ;
Thompson, John .
STATISTICS IN MEDICINE, 2017, 36 (11) :1783-1802
[3]   Consistent Estimation in Mendelian Randomization with Some Invalid Instruments Using a Weighted Median Estimator [J].
Bowden, Jack ;
Smith, George Davey ;
Haycock, Philip C. ;
Burgess, Stephen .
GENETIC EPIDEMIOLOGY, 2016, 40 (04) :304-314
[4]   Mendelian randomization with invalid instruments: effect estimation and bias detection through Egger regression [J].
Bowden, Jack ;
Smith, George Davey ;
Burgess, Stephen .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2015, 44 (02) :512-525
[5]  
Burgess Stephen, 2019, Wellcome Open Res, V4, P186, DOI 10.12688/wellcomeopenres.15555.3
[6]   Bias due to participant overlap in two-sample Mendelian randomization [J].
Burgess, Stephen ;
Davies, Neil M. ;
Thompson, Simon G. .
GENETIC EPIDEMIOLOGY, 2016, 40 (07) :597-608
[7]  
Chalasani NP, 2017, HEPATOLOGY, V66, p303A
[8]   A systematic review and a dose-response meta-analysis of coffee dose and nonalcoholic fatty liver disease [J].
Chen, Yong-Ping ;
Lu, Feng-Bin ;
Hu, Yi-Bing ;
Xu, Lan-Man ;
Zheng, Ming-Hua ;
Hu, En-De .
CLINICAL NUTRITION, 2019, 38 (06) :2552-2557
[9]   The Causal Relationships Between Sleep-related Phenotypes and Body Composition: A Mendelian Randomized Study [J].
Chen, Yujing ;
Li, Chun'e ;
Cheng, Shiqiang ;
Pan, Chuyu ;
Zhang, Huijie ;
Zhang, Jingxi ;
Zhang, Zhen ;
Yao, Yao ;
Cheng, Bolun ;
Liu, Li ;
Meng, Peilin ;
Yang, Xuena ;
Jia, Yumeng ;
Wen, Yan ;
Zhang, Feng .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2022, 107 (08) :E3463-E3473
[10]   Exploiting horizontal pleiotropy to search for causal pathways within a Mendelian randomization framework [J].
Cho, Yoonsu ;
Haycock, Philip C. ;
Sanderson, Eleanor ;
Gaunt, Tom R. ;
Zheng, Jie ;
Morris, Andrew P. ;
Smith, George Davey ;
Hemani, Gibran .
NATURE COMMUNICATIONS, 2020, 11 (01)