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Association of glp-1 receptor agonist prescriptions and alcohol consumption in the national institutes of health's all of us cohort
Tyndall, B., Gasdaska, A., Brannock, M. D., Preble, E., McPheeters, M., Marcial, L., Huda, A., Egan, J., Litwin, T. R., Adjemian, J., Sastry, C., Farokhnia, M., & Leggio, L. (2026). Association of glp-1 receptor agonist prescriptions and alcohol consumption in the national institutes of health's all of us cohort. medRxiv : the preprint server for health sciences. Advance online publication. https://doi.org/10.64898/2026.01.15.26344218
IMPORTANCE: Alcohol use is a leading cause of morbidity and mortality worldwide. Growing evidence suggests that glucagon-like peptide-1 receptor agonists (GLP-1RAs) may represent a novel potential pharmacotherapeutic tool for alcohol use disorder (AUD).
OBJECTIVE: To examine the association between GLP-1RA prescriptions and alcohol use.
DESIGN: This cohort study used a cross-sectional measure of alcohol consumption and longitudinal electronic health record (EHR) data collected between 1981 and October 2023 from NIH's All of Us Research Program participants.
SETTING: All of Us is a large program to recruit and collect surveys, EHR, genomic, and wearable data from a wide array of Americans. The data presented here are from the All of Us Curated Data Repository version 8.
PARTICIPANTS: 393,596 All of Us participants with EHR data recruited across the United States.
EXPOSURE: At least two GLP-1RA prescription records in the EHR.
MAIN OUTCOMES AND MEASURES: Alcohol Use Disorders Identification Test (AUDIT-C) scores and responses to individual AUDIT-C questions.
RESULTS: Among 15,447 participants with at least two recorded GLP-1RA prescriptions on separate days, 3650 had active GLP-1RA prescriptions, 5642 would have future GLP-1RA prescriptions (primary comparison group), and 544 had former GLP-1RA prescriptions. Those with active GLP-1RA prescriptions had statistically significant but modestly lower AUDIT-C scores on average compared with those with future prescriptions (incidence rate ratio [IRR] of 0.95; 95% CI, 0.91-0.99; P = 0.01). Participants with a former GLP-1RA prescription had lower AUDIT-C scores compared with those with future prescriptions, but this difference was not statistically significant. Results were similar using a propensity-score matched comparison group with a lower average AUDIT-C score for the current GLP-1RA group (IRR = 0.89; 95% CI, 0.85-0.93; P = <0.001) and no significant difference for the former prescription group. Analysis of individual AUDIT-C questions shows a significant association with GLP-1RA prescriptions and frequency of drinking but not drinks per occasion or binge drinking.
CONCLUSIONS AND RELEVANCE: This study's findings indicate that GLP-1RAs may reduce alcohol consumption by decreasing use frequency. Experimental studies and randomized controlled trials are needed to test the mechanisms and potential efficacy of GLP-1RAs in people with AUD.
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