PPAR-alpha/gamma agonists, glucagon-like peptide-1 receptor agonists and metformin for non-alcoholic fatty liver disease: A network meta-analysis

J Int Med Res. 2023 Jun;51(6):3000605231177191. doi: 10.1177/03000605231177191.

Abstract

Objective: To undertake a network meta-analysis to compare the relative efficacy of a dual peroxisome proliferator-activated receptor (PPAR)α and PPARγ agonist, glucagon-like peptide-1 receptor agonists (GLP-1RAs) and metformin in patients with non-alcoholic fatty liver disease (NAFLD).

Methods: Electronic databases, including Embase®, PubMed® and The Cochrane Library, were searched systematically for eligible studies from inception to 20 July 2022. Randomized controlled trials (RCTs) that investigated aspartate aminotransferase, alanine aminotransferase (ALT) and triglyceride levels were considered for inclusion. Data were extracted using a standardized data collection table. A network meta-analysis was performed. Relative risk and 95% confidence interval were calculated for continuous data and I2 was used to assess the heterogeneity of studies.

Results: A total of 22 RCTs involving 1698 patients were eligible for inclusion in the analysis. Both direct analysis and indirect analysis showed that saroglitazar was significantly superior to GLP-1RAs in improving ALT levels. Metformin improved ALT levels, but the effect was not as good as saroglitazar.

Conclusion: Saroglizatar was the most effective drug for improving NAFLD.INPLASY registration number: INPLASY202340066.

Keywords: NAFLD; glucagon-like peptide-1 receptor agonists; metformin; saroglizatar.

Publication types

  • Meta-Analysis

MeSH terms

  • Glucagon-Like Peptide-1 Receptor
  • Humans
  • Metformin* / therapeutic use
  • Network Meta-Analysis
  • Non-alcoholic Fatty Liver Disease* / drug therapy
  • Peroxisome Proliferator-Activated Receptors

Substances

  • Metformin
  • saroglitazar
  • Glucagon-Like Peptide-1 Receptor
  • Peroxisome Proliferator-Activated Receptors