Association of PNPLA3 SNP With the Development of HBV-related Hepatocellular Carcinoma

In Vivo. 2023 Mar-Apr;37(2):763-770. doi: 10.21873/invivo.13139.

Abstract

Background/aim: Concomitant nonalcoholic fatty liver disease (NAFLD)/hepatic steatosis (HS) is suggested to increase the risk of hepatocellular carcinoma (HCC) in hepatitis virus B (HBV)-infected patients. Patatin-like phospholipase domain-containing 3 (PNPLA3) rs738409 gene single-nucleotide polymorphism (SNP) is well-known to be associated with the development of NAFLD/HS; however, it is still unclear whether this SNP is related to the development of HCC in HBV-infected patients.

Patients and methods: We investigated a total of 202 HBV-infected patients who received percutaneous liver biopsy, and simultaneously assessed biopsy-proven HS, insulin resistance, and the PNPLA3 SNP status. We further investigated the relationships of these factors with the development of HCC in HBV-infected patients.

Results: Most of the enrolled cases (196/202: 97.0%) were non-cirrhotic patients. One hundred seventy-three patients (85.6%) received antiviral therapy. A Kaplan-Meier analysis showed that the incidence of HCC development in patients with HS was higher than that in patients without HS (p<0.01). An increased homeostasis model assessment as an index of insulin resistance (HOMA-IR) value (≥1.6) was associated not only with the presence of HS (p<0.0001) but also with the development of HCC (p<0.01). The PNPLA3 rs738409 SNP was also associated with the presence of HS (p<0.01) and the development of HCC (p<0.05) in HBV-infected patients.

Conclusion: In addition to HS and IR, PNPLA3 rs738409 SNP was suggested to be associated with the development of HCC in Japanese patients with HBV infection.

Keywords: HBV; HOMA-IR; PNPLA3; hepatic steatosis; hepatocellular carcinoma.

MeSH terms

  • Carcinoma, Hepatocellular* / genetics
  • Hepatitis B virus / genetics
  • Humans
  • Insulin Resistance*
  • Liver Neoplasms* / genetics
  • Non-alcoholic Fatty Liver Disease* / complications
  • Non-alcoholic Fatty Liver Disease* / genetics
  • Phospholipases A2, Calcium-Independent* / genetics
  • Polymorphism, Single Nucleotide

Substances

  • PNPLA3 protein, human
  • Phospholipases A2, Calcium-Independent