Binge-pattern alcohol consumption and genetic risk as determinants of alcohol-related liver disease

被引:1
|
作者
Ding, Chengyi [1 ]
Ng Fat, Linda [2 ]
Britton, Annie [2 ]
Im, Pek Kei [3 ]
Lin, Kuang [3 ]
Topiwala, Anya [4 ]
Li, Liming [5 ,6 ,7 ]
Chen, Zhengming [3 ,8 ]
Millwood, Iona Y. [3 ,8 ]
Bell, Steven [9 ,10 ]
Mehta, Gautam [11 ,12 ,13 ]
机构
[1] UCL, Div Psychiat, London, England
[2] UCL, Res Dept Epidemiol & Publ Hlth, London, England
[3] Univ Oxford, Nuffield Dept Populat Hlth, Clin Trial Serv Unit & Epidemiol Studies Unit CTSU, Oxford, England
[4] Univ Oxford, Big Data Inst, Nuffield Dept Populat Hlth, Oxford, England
[5] Peking Univ Hlth Sci Ctr, Sch Publ Hlth, Dept Epidemiol & Biostat, Beijing, Peoples R China
[6] Peking Univ, Key Lab Epidemiol Major Dis, Minist Educ, Beijing, Peoples R China
[7] Peking Univ, Ctr Publ Hlth & Epidem Preparedness & Response, Beijing, Peoples R China
[8] Univ Oxford, Med Res Council Populat Hlth Res Unit MRC PHRU, Nuffield Dept Populat Hlth, Oxford, England
[9] Univ Cambridge, Precis Breast Canc Inst, Dept Oncol, Cambridge, England
[10] Univ Cambridge, Canc Res UK Cambridge Ctr, Li Ka Shing Ctr, Cambridge, England
[11] UCL, Inst Liver & Digest Hlth, London, England
[12] Fdn Liver Res, Roger Williams Inst Hepatol, London, England
[13] Royal Free London NHS Fdn Trust, London, England
基金
英国惠康基金; 中国国家自然科学基金; 美国国家卫生研究院; 英国医学研究理事会;
关键词
CIRRHOSIS; DRINKING; MORTALITY;
D O I
10.1038/s41467-023-43064-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Alcohol-related liver disease (ARLD) represents a major public health burden. Identification of high-risk individuals would allow efficient targeting of public health interventions. Here, we show significant interactions between pattern of drinking, genetic predisposition (polygenic risk score, PRS) and diabetes mellitus, and risk of incident ARLD, in 312,599 actively drinking adults in UK Biobank. Binge and heavy binge drinking significantly increase the risk of alcohol-related cirrhosis (ARC), with higher genetic predisposition further amplifying the risk. Further, we demonstrate a pronounced interaction between heavy binge drinking and high PRS, resulting in a relative excess risk due to interaction (RERI) of 6.07. Diabetes consistently elevates ARC risk across all drinking and PRS categories, and showed significant interaction with both binge patterns and genetic risk. Overall, we demonstrate synergistic effects of binge drinking, genetics, and diabetes on ARC, with potential to identify high-risk individuals for targeted interventions. Deaths from alcohol-related liver disease have sharply increased following the Covid-19 pandemic. Here, the authors show that binge-pattern alcohol consumption, genetic factors and the presence of diabetes mellitus confer the greatest risk, allowing targeted interventions for high-risk individuals.
引用
收藏
页数:8
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