Insights from Genome-Wide Association Analyses of Nonalcoholic Fatty Liver Disease

被引:49
作者
Kahali, Bratati [1 ]
Halligan, Brian [1 ]
Speliotes, Elizabeth K. [1 ]
机构
[1] Univ Michigan, Dept Internal Med, Div Gastroenterol, Dept Computat Med & Bioinformat, Ann Arbor, MI 48109 USA
关键词
nonalcoholic liver disease; nonalcoholic steatohepatitis; gene; genetics; polymorphism; CHRONIC HEPATITIS-C; HEPATOCELLULAR-CARCINOMA OCCURRENCE; NORTH-AMERICAN PATIENTS; PNPLA3 I148M RS738409; THAN-G POLYMORPHISM; FIBROSIS PROGRESSION; GENETIC-VARIATION; PROTEIN PHOSPHATASE-1; HISTOLOGIC FEATURES; REGULATORY PROTEIN;
D O I
10.1055/s-0035-1567870
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Nonalcoholic fatty liver disease (NAFLD) is caused by hepatic steatosis, which can progress to nonalcoholic steatohepatitis, fibrosis/ cirrhosis, and hepatocellular carcinoma in the absence of excessive alcohol consumption. Nonalcoholic fatty liver disease will become the number one cause of liver disease worldwide by 2020. Nonalcoholic fatty liver disease is correlated albeit imperfectly with obesity and other metabolic diseases such as diabetes, hyperlipidemia, and cardiovascular disease, but exactly how having one of these diseases contributes to the development of othermetabolic diseases is only now being elucidated. Development of NAFLD and related metabolic diseases is genetically influenced in the population, and recent genome-wide association studies (GWASs) have discovered genetic variants that associate with these diseases. These GWAS-associated variants cannot only help us to identify individuals at high risk of developing NAFLD, but also to better understand its pathophysiology so that we can developmore effective treatments for this disease and relatedmetabolic diseases in the future.
引用
收藏
页码:375 / 391
页数:17
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