Genetic and lifestyle risk factors for advanced liver disease among men and women

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Sahlman , P , Nissinen , M , Puukka , P , Jula , A , Salomaa , V , Männistö , S , Lundqvist , A , Valsta , L , Perola , M , Färkkilä , M & Åberg , F 2019 , ' Genetic and lifestyle risk factors for advanced liver disease among men and women ' , Journal of Gastroenterology and Hepatology . https://doi.org/10.1111/jgh.14770

Title: Genetic and lifestyle risk factors for advanced liver disease among men and women
Author: Sahlman, Perttu; Nissinen, Markku; Puukka, Pauli; Jula, Antti; Salomaa, Veikko; Männistö, Satu; Lundqvist, Annamari; Valsta, Liisa; Perola, Markus; Färkkilä, Martti; Åberg, Fredrik
Contributor: University of Helsinki, HUS Abdominal Center
University of Helsinki, HUS Abdominal Center
University of Helsinki, INDIVIDRUG - Individualized Drug Therapy
University of Helsinki, National Institute for Health and Welfare (THL)
University of Helsinki, Centre of Excellence in Complex Disease Genetics
University of Helsinki, Staff Services
Date: 2019-07-28
Language: eng
Number of pages: 8
Belongs to series: Journal of Gastroenterology and Hepatology
ISSN: 0815-9319
URI: http://hdl.handle.net/10138/312970
Abstract: Background and Aim Liver disease is traditionally categorized as alcoholic and non-alcoholic. We studied various risk factors predictive of advanced non-viral liver disease in general population and analyzed the interaction between these factors and alcohol consumption. Methods Persons without underlying liver disease who participated in the Health2000 or FINRISK studies 1992-2012 comprised a cohort of 41 260 individuals. Pattern of alcohol consumption and metabolic, lifestyle-related, and anthropometric parameters were analyzed with Cox regression analysis using severe liver disease hospitalization, cancer, or death as end-point. Viral liver diseases were excluded. Results A total of 355 liver events occurred during the mean 12.4-year follow-up (511 789 person-years). In the multivariate model, age (hazard ratio [HR] 1.03, P = 0.0083 for men; HR 1.04, P = 0.0198 for women), waist-to-hip ratio (WHR) (HR 1.52, P = 0.0006 for men; HR 1.58, P = 0.0167 for women), patatin-like phospholipase-containing domain 3 mutations (HR 1.9, P = 0.024 for men; HR 2.7, P = 0.0109 for women), and weekly binge drinking (HR 2.4, P = 0.0024 for men; HR 7.4, P <0.0001 for women) predicted development of severe liver disease. Among men, diabetes (HR 2.7, P = 0.0002), average alcohol consumption (HR for 10 g/day 1.1, P = 0.0022), non-married status (HR 1.9, P = 0.0397 for single; HR 2.4, P = 0.0002 for widowed/separated), and serum high-density lipoprotein (HR 2.2, P = 0.0022) and non-high-density lipoprotein cholesterol (HR 1.2, P = 0.0237) were additional risk factors. Alcohol intake increased the risk especially among persons with high WHR (P for interaction 0.009). Conclusions Age, patatin-like phospholipase-containing domain 3 haplotype, and WHR increase the risk for development of severe liver disease. We found strong synergism between alcohol and central obesity. Binge drinking is an additional risk factor.
Subject: Alcohol
Cirrhosis
Liver disease
Risk factor
BODY-MASS INDEX
ALCOHOL-CONSUMPTION
METABOLIC SYNDROME
CIRRHOSIS
MORTALITY
OBESITY
METAANALYSIS
ASSOCIATION
DRINKING
FIBROSIS
3121 General medicine, internal medicine and other clinical medicine
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