Metformin in patients with non-alcoholic fatty liver disease: A randomized, controlled trial
Abstract
OBJECTIVE: The antidiabetic agent metformin is regularly discussed as a promising treatment for non-alcoholic fatty liver disease (NAFLD), which is characterized by insulin resistance. However, the evidence for its beneficial effects is limited, and conflicting reports have been published. The purpose of this study was to conduct a randomized, double-blind, placebo-controlled trial to test whether metformin improves liver histology in patients with non-alcoholic fatty liver disease. MATERIAL AND METHODS: Forty-eight patients with biopsy-proven NAFLD were randomized to treatment with metformin (n=24) or placebo (n=24) for 6 months. A second liver biopsy was obtained in all subjects who completed the trial (n=44). Data analyses are restricted to this group (per-protocol analyses). The primary outcome was changes in histologically assessed liver steatosis. Secondary outcomes were changes in NAFLD activity (NAS)-score, liver steatosis assessed by computed tomography (CT), liver transaminases, body-weight, metabolic variables and inflammatory markers. RESULTS: No significant differences between treatment with metformin or placebo were observed for changes in liver steatosis, assessed either histologically or by CT, NAS-score, liver transaminases or on markers of insulin resistance or inflammation. In contrast, beneficial effects of metformin were observed on changes in body-weight (p<0.001), serum levels of cholesterol (p=0.004), LDL-cholesterol (p<0.001), glucose (p=0.032) and on HbA1c (p=0.020). CONCLUSIONS: Treatment with metformin for 6 months was no better than placebo in terms of improvement in liver histology in patients with NAFLD. Nevertheless, the use of metformin could still be beneficial in this group as it is associated with a reduction in serum levels of lipids and glucose. (ClinicalTrials.gov number, NCT00303537).
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Concerning cost effectiveness, resmetirom provides a yet unpredictable burden for health care system, while MAESTRO trials hint to large placebo-corrected numbers needed to treat (approximately 2 of 10 patients treated will have MASH resolution and 1 of 10 patients treated will improve in liver fibrosis).
“Concerning cost effectiveness, resmetirom provides a yet unpredictable burden for the health care system, while the MAESTRO trials hint to large placebo-corrected numbers needed to treat (approximately 2 of 10 patients treated will have MASH resolution and 1 of 10 patients treated will improve in liver fibrosis) [243].”
From Obesity and MASLD: Is weight loss the (only) key to treat metabolic liver disease? (2024) · cites this paper as [243]
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References 25 · Cited by 323
- Authors
- Haukeland, J. W., Konopski, Z., Eggesbø, H. B., von Volkmann, H. L., Raschpichler, G., Bjøro, K., Haaland, T., Løberg, E. M., & Birkeland, K.
- Affiliations
- University of Oslo (NO)
- Oslo University Hospital (NO)
- University Hospital of North Norway (NO)
- Corresponding author
- Haukeland, John Willy
- Venue
- Scandinavian Journal of Gastroenterology
- Publisher
- Informa UK Limited
- Published
- 2009-01
- Volume
- 44
- Issue
- 7
- Pages
- 853-860
- ISSN
- 0036-5521 (ISSN-L)
- 1502-7708
- OpenAlex
- W2059196301
- Cited by
- 323
- References
- 25
- Citations by year
- 2026: 4 · 2025: 14 · 2024: 15 · 2023: 13 · 2022: 22 · 2021: 35 · 2020: 27 · 2019: 18 · 2018: 23 · 2017: 12 · 2016: 20 · 2015: 28 · 2014: 27 · 2013: 23 · 2012: 14
- FWCI
- 9.22
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Scandinavian Journal of Gastroenterology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of South Australia
- Topics
- Health Sciences › Medicine › Epidemiology › Liver Disease Diagnosis and Treatment
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Keywords
- metformin, non-alcoholic fatty liver disease, insulin resistance, hepatic steatosis, NAFLD activity score, liver histopathology, weight loss, serum lipids, glycemic control, HbA1c, liver transaminases, inflammatory markers
- MeSH terms
- Administration, Oral, Adult, Biopsy, Double-Blind Method, Enzyme-Linked Immunosorbent Assay, Fatty Liver, Female, Humans, Hypoglycemic Agents, Liver Function Tests, Male, Metformin, Middle Aged, Placebos, Tomography, X-Ray Computed, Linear Models, Treatment Outcome, Statistics, Nonparametric
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