Combined Effect of PNPLA3, TM6SF2, and HSD17B13 Variants on Risk of Cirrhosis and Hepatocellular Carcinoma in the General Population

• Published in: Hepatology (Baltimore, Md.) Vol. 72; no. 3; pp. 845 - 856
• Main Authors: Gellert‐Kristensen, Helene, Richardson, Tom G., Davey Smith, George, Nordestgaard, Børge G., Tybjærg‐Hansen, Anne, Stender, Stefan
• Format: Journal Article
• Language: English
• Published: United States Wolters Kluwer Health, Inc 01.09.2020
• Subjects: 17-Hydroxysteroid Dehydrogenases - genetics; Alanine; Alanine transaminase; Alanine Transaminase - blood; Biobanks; Carcinoma, Hepatocellular - blood; Carcinoma, Hepatocellular - epidemiology; Carcinoma, Hepatocellular - genetics; Cirrhosis; Denmark - epidemiology; Fatty liver; Female; Genetic diversity; Genetic Predisposition to Disease; Health risk assessment; Hepatocellular carcinoma; Hepatology; Humans; Lipase - genetics; Liver cancer; Liver cirrhosis; Liver Cirrhosis - blood; Liver Cirrhosis - epidemiology; Liver Cirrhosis - genetics; Liver diseases; Liver Neoplasms - blood; Liver Neoplasms - epidemiology; Liver Neoplasms - genetics; Male; Membrane Proteins - genetics; Middle Aged; Non-alcoholic Fatty Liver Disease - blood; Non-alcoholic Fatty Liver Disease - diagnosis; Non-alcoholic Fatty Liver Disease - epidemiology; Phospholipase; Polymorphism, Single Nucleotide; Risk Factors; United Kingdom - epidemiology; Denmark; United Kingdom; United Kingdom > UK
• ISSN: 0270-9139; 1527-3350; 1527-3350
• DOI: 10.1002/hep.31238

Background and Aims We hypothesized that a genetic risk score (GRS) for fatty liver disease influences the risk of cirrhosis and hepatocellular carcinoma (HCC). Three genetic variants (patatin‐like phospholipase domain–containing protein 3 [PNPLA3] p.I148M; transmembrane 6, superfamily member 2 [TM6SF2] p.E167K; and hydroxysteroid 17‐beta dehydrogenase 13 [HSD17B13] rs72613567) were combined into a risk score, ranging from 0 to 6 for risk‐increasing alleles. Approach and Results We examined the association of the risk score with plasma markers of liver disease and with cirrhosis and HCC in 110,761 individuals from Copenhagen, Denmark, and 334,691 individuals from the UK Biobank. The frequencies of risk scores of 0, 1, 2, 3, 4, and 5 or 6 were 5%, 25%, 41%, 23%, 5.5%, and 0.5%, respectively. A higher GRS was associated with an increase in plasma alanine aminotransferase (ALT) level of 26% in those with score 5 or 6 versus 0. In meta‐analysis of the Copenhagen studies and the UK Biobank, individuals with scores 1, 2, 3, 4, and 5 or 6 had odds ratios (ORs) for cirrhosis of 1.6 (95% confidence interval [CI], 1.3, 1.9), 2.0 (95% CI, 1.8, 2.2), 3.1 (95% CI, 2.7, 3.5), 5.2 (95% CI, 4.2, 6.4), and 12 (95% CI, 7.7, 19), respectively, as compared with those with a score of 0. The corresponding ORs for HCC were 1.2 (95% CI, 0.9, 1.7), 1.0 (95% CI, 0.7, 1.3), 2.4 (95% CI, 1.9, 3.0), 3.3 (95% CI, 2.2, 5.0), and 29 (95% CI, 17, 51). Conclusion A GRS for fatty liver disease confers up to a 12‐fold higher risk of cirrhosis and up to a 29‐fold higher risk of HCC in individuals from the general population.