Impact of PNPLA3 I148M on Drug-Induced Hepatocellular Liver Injury: A Systematic Review and Meta-Analysis.

Alexandra Gatzios, Lorna Marchandise, Hannes Hagström, Jörn M Schattenberg, Robim M Rodrigues, Tamara Vanhaecke, Joost Boeckmans

Journal: Liver international : official journal of the International Association for the Study of the Liver 2025;45(9):e70287

PMID: 40851509

Abstract

BACKGROUND AND AIMS

The role of the patatin-like phospholipase domain-containing protein 3 (PNPLA3)-I148M variant in drug-induced liver injury (DILI) remains unclear. This systematic review with meta-analysis investigated whether carriage of PNPLA3 I148M may contribute to the development of hepatocellular DILI.

METHODS

Scientific databases were searched up to January 31st, 2025 for studies investigating serum transaminase elevations in response to drug treatment. Studies were included if serum transaminases were elevated in at least one genetic subgroup (II/IM/MM), and the possible presence of relevant hepatocellular DILI was estimated based on Hy's law. The meta-analysis reported on any increase in transaminases compared to baseline levels.

RESULTS

Eight articles covering thirteen studies with a total of 8235 patients were included in the systematic review, of which 5 studies comprising 3480 individuals were eligible for the meta-analysis. Patients were treated with small molecules (n = 602), biologicals (n = 3221), or chemotherapeutic treatments (n = 4412). None of the studies reported conclusively more occurrence of relevant hepatocellular DILI based on PNPLA3 I148M carriage. The meta-analysis suggested amplified drug-induced transaminase elevations in response to adomeglivant and basal insulin peglispro in metabolically impaired individuals with PNPLA3-IM/MM compared to PNPLA3-II (odds ratio = 1.53, 95% CI = 1.22-1.92). None of the studies were primarily designed to detect the outcome of interest.

CONCLUSIONS

Low to no evidence suggests that carriage of PNPLA3 I148M confers susceptibility to develop clinically relevant hepatocellular DILI; although it may potentiate drug-induced transaminase elevations in response to adomeglivant and basal insulin peglispro in metabolically impaired individuals.

© 2025 The Author(s). Liver International published by John Wiley & Sons Ltd.

Address: In Vitro Liver Disease Modelling Team, Department of In Vitro Toxicology & Dermato-Cosmetology, Faculty of Medicine & Pharmacy, Vrije Universiteit Brussel, Brussels, Belgium.; Department of Medicine, Huddinge, Karolinska Institutet, Stockholm, Sweden.; Division of Hepatology, Department of Upper GI, Karolinska University Hospital, Stockholm, Sweden.; Department of Medicine II, University Medical Center Homburg, Homburg and Saarland University, Saarbrücken, Germany.

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