Carriage of the PNPLA3 rs738409 C >G polymorphism confers an increased risk of non-alcoholic fatty liver disease associated hepatocellular carcinoma

JOURNAL OF HEPATOLOGY

卷:61

Article

Liu, Y. -L.¹  Patman, G. L.²  Leathart, J. B. S.¹  Piguet, A. -C.³  Burt, A. D.¹  Dufour, J. -F.³  Day, C. P.¹  Daly, A. K.¹  Reeves, H. L.²  Anstee, Q. M.¹ 

[1] Newcastle Univ, Sch Med, Inst Cellular Med, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England

[2] Newcastle Univ, Sch Med, Northern Inst Canc Res, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England

[3] Inselspital Bern, Univ Clin Visceral Surg & Med, CH-3010 Bern, Switzerland

关键词: NAFLD;    NASH;    Steatohepatitis;    PNPLA3;    Hepatocellular carcinoma;    HCC;    Gene;   

DOI  :  10.1016/j.jhep.2014.02.030

来源: Elsevier

【 摘 要 】

Background & Aims: Subtle inter-patient genetic variation and environmental factors combine to determine disease progression in non-alcoholic fatty liver disease (NAFLD). Carriage of the PNPLA3 rs738409 c.444C >G minor allele (encoding the I148M variant) has been robustly associated with advanced NAFLD. Although most hepatocellular carcinoma (HCC) is related to chronic viral hepatitis or alcoholic liver disease, the incidence of NAFLD-related HCC is increasing. We examined whether rs738409 C >G was associated with HCC-risk in patients with NAFLD. Methods: PNPLA3 rs738409 genotype was determined by allelic discrimination in 100 European Caucasians with NAFLD-related HCC and 275 controls with histologically characterised NAFLD. Results: Genotype frequencies were significantly different between NAFLD-HCC cases (CC = 28, CG = 43, GG = 29) and NAFLD-controls (CC = 125, CG = 117, GG = 33) (p = 0.0001). In multivariate analysis adjusted for age, gender, diabetes, BMI, and presence of cirrhosis, carriage of each copy of the rs738409 minor (G) allele conferred an additive risk for HCC (adjusted OR 2.26 [95% CI 1.23-4.14], p = 0.0082), with GG homozygotes exhibiting a 5-fold [1.47-17.29], p = 0.01 increased risk over CC. When compared to the UK general population (1958 British Birth Cohort, n = 1476), the risk-effect was more pronounced (GC vs. CC: unadjusted OR 2.52 [1.55-4.10], p = 0.0002; GG vs. CC: OR 12.19 [6.89-21.58], p <0.0001). Conclusions: Carriage of the PNPLA3 rs738409 C >G polymorphism is not only associated with greater risk of progressive steatohepatitis and fibrosis but also of HCC. If validated, these findings suggest that PNPLA3 genotyping has the potential to contribute to multi-factorial patient-risk stratification, identifying those to whom HCC surveillance may be targeted. (C) 2014 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

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