Metformin in non-alcoholic fatty liver disease: A systematic review and meta-analysis
Open accessAbstract
Non-alcoholic fatty liver disease (NAFLD) related to insulin resistance (IR) is a growing global health concern. Recent studies have indicated that metformin could improve IR and may be beneficial in the treatment of NAFLD. This study aimed to assess the beneficial or harmful effects of metformin in NAFLD. We searched Medline and four other databases during April 2012. Selection criteria were randomized clinical trials comparing metformin with placebo or other interventions for treating NAFLD patients. The primary outcome was histological response. The secondary outcomes included alanine aminotransferase (ALT), aspartate aminotransferase (AST), homeostasis model assessment of IR (HOMA‑IR), body mass index (BMI) and adverse events. Dichotomous data were reported as odds ratio (OR), while continuous data were calculated as the mean difference (MD), both with 95% confidence intervals (CI). Random and fixed effects meta-analyses were performed. Nine studies were included, involving 417 participants, and conducted for a time period ranging from 4 to 12 months. In the treated participants, improvements were observed in ALT (MD, -8.12 U/l; P=0.03), AST (MD, -4.52 U/l; P=0.04), HOMA‑IR (MD, -0.61; P=0.005) and BMI (MD, -0.82 kg/m2; P=0.04), but not in histological response: steatosis (P=0.66), inflammation (P=0.91), hepatocellular ballooning (P=0.25) and fibrosis (P=0.90). Sub‑analysis of non‑alcoholic fatty steatohepatitis showed that metformin failed to improve any pooled outcome. Adverse events were poorly reported. Current information indicates that metformin improves liver function, HOMA‑IR and BMI to some extent, but not histological response in NAFLD patients. This finding could serve as a stimulus for future studies investigating issues such as dose‑responsiveness, safety and patient tolerance to metformin therapy.
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Metformin exerts glucose-lowering effects by multiple mechanisms, including reduction of hepatic gluconeogenesis.
“Metformin, exerting its glucose-lowering effects by multiple mechanisms, including reduction of hepatic gluconeogenesis [165], received approval for treatment of type 2 diabetes already in the 1960's; thus, no respective cardiovascular outcome trials (CVOTs) have been conducted.”
From Obesity and MASLD: Is weight loss the (only) key to treat metabolic liver disease? (2024) · cites this paper as [165]
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- Authors
- LI, Y., LIU, L., WANG, B., WANG, J., & CHEN, D.
- Affiliations
- Army Medical University (CN)
- Venue
- Biomedical Reports
- Publisher
- Spandidos Publications
- Published
- 2012-10-09
- Volume
- 1
- Issue
- 1
- Pages
- 57-64
- ISSN
- 2049-9434 (ISSN-L)
- 2049-9442
- PMC
- PMC3956897
- OpenAlex
- W1976509021
- Cited by
- 290
- References
- 4
- Citations by year
- 2026: 14 · 2025: 18 · 2024: 23 · 2023: 44 · 2022: 42 · 2021: 36 · 2020: 39 · 2019: 29 · 2018: 16 · 2017: 9 · 2016: 11 · 2015: 5 · 2014: 2
- FWCI
- 0.28
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Biomedical Reports (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Natural Science Foundation of China (81072362, 81200297)
- Topics
- Health Sciences › Medicine › Epidemiology › Liver Disease Diagnosis and Treatment
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- metformin, non-alcoholic fatty liver disease, insulin resistance, nonalcoholic steatohepatitis, histological response, alanine aminotransferase, aspartate aminotransferase, HOMA-IR, body mass index, liver fibrosis, steatosis, hepatocyte ballooning, adverse events
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