Impact of GLP-1 Receptor Agonists on Alcohol-Related Liver Disease Development and Progression in Alcohol Use Disorder
- PMID: 39891379
- DOI: 10.1111/apt.70007
Impact of GLP-1 Receptor Agonists on Alcohol-Related Liver Disease Development and Progression in Alcohol Use Disorder
Abstract
Background and aims: Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have shown promise in reducing alcohol consumption, but their impact on clinical outcomes in patients with alcohol use disorder (AUD) remains unclear. We investigated the association between GLP-1RAs and the development and progression of alcohol-related liver disease (ArLD) in patients with AUD.
Methods: Using the TriNetX Research Network, we conducted two retrospective cohort studies comparing GLP-1RAs versus dipeptidyl peptidase-4 inhibitors (DPP-4is) in patients with type 2 diabetes. The first cohort included patients with AUD but without ArLD (n = 7132 after propensity score matching), while the second comprised patients with established ArLD (n = 1896 after matching). Primary outcomes were incident ArLD in the AUD cohort and hepatic decompensation in the ArLD cohort.
Results: In the AUD cohort (median follow-up: 63.2 months), GLP-1RA users showed significantly lower risks of developing ArLD compared to DPP-4i users (incidence rate: 6.0 vs. 8.7 per 1000 person-years; HR: 0.62, 95% CI: 0.44-0.87, p = 0.006). GLP-1RAs were also associated with reduced risks of all-cause mortality (HR: 0.53, p < 0.001). In the ArLD cohort (median follow-up: 28.2 months), GLP-1RA users demonstrated lower risks of hepatic decompensation (incidence rate: 39.5 vs. 51.4 per 1000 person-years; HR: 0.66, 95% CI: 0.51-0.85, p = 0.001) and all-cause mortality (HR: 0.53, p < 0.001) compared to DPP-4i users.
Conclusions: GLP-1RAs were associated with reduced risks of developing and progressing ArLD in patients with AUD, suggesting potential therapeutic benefits in this population.
Keywords: alcohol use disorder; alcohol‐related liver disease; glucagon‐like peptide‐1 receptor agonists; mortality; real‐world evidence.
© 2025 John Wiley & Sons Ltd.
References
-
- J. P. Connor, P. S. Haber, and W. D. Hall, “Alcohol Use Disorders,” Lancet 387, no. 10022 (2016): 988–998.
-
- H. Y. Choi, D. R. Balter, and L. Y. Haque, “Epidemiology and Health Care Burden of Alcohol Use Disorder,” Clinics in Liver Disease 28, no. 4 (2024): 577–588.
-
- Substance Abuse and Mental Health Services Administration, “Key Substance Use and Mental Health Indicators in the United States: Results from the 2022 National Survey on Drug Use and Health,” accessed October 12, 2024, https://www.samhsa.gov/data/sites/default/files/reports/rpt42731/2022‐ns....
-
- A. F. Carvalho, M. Heilig, A. Perez, C. Probst, and J. Rehm, “Alcohol Use Disorders,” Lancet (London, England) 394, no. 10200 (2019): 781–792.
-
- J. Rehm, A. V. Samokhvalov, and K. D. Shield, “Global Burden of Alcoholic Liver Diseases,” Journal of Hepatology 59, no. 1 (2013): 160–168.
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