Evidence mapPaperPMID 42423024Full record

ArticleAlcohol, clinical & experimental research2026

Association of GLP-1 Receptor Agonist Prescriptions and Alcohol Consumption in the National Institutes of Health's All of Us Cohort.

Benjamin Tyndall, Angela Gasdaska, M Daniel Brannock, Ed Preble, Melissa McPheeters, Laura Marcial, Ariba Huda, Josephine Egan, Tamara R Litwin, Jennifer Adjemian and 3 more

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Article in Alcohol, clinical & experimental research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Benjamin TyndallRTI International, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0001-5514-4149
Angela GasdaskaRTI International, Durham, North Carolina, USA.
M Daniel BrannockRTI International, Durham, North Carolina, USA.
Ed PrebleRTI International, Durham, North Carolina, USA.
Melissa McPheetersRTI International, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0002-4423-797X
Laura MarcialRTI International, Durham, North Carolina, USA.
Ariba HudaRTI International, Durham, North Carolina, USA.
Josephine EganNational Institutes of Health, Bethesda, Maryland, USA.
Tamara R LitwinNational Institutes of Health, Bethesda, Maryland, USA.
Jennifer AdjemianNational Institutes of Health, Bethesda, Maryland, USA.
Chandan SastryNational Institutes of Health, Bethesda, Maryland, USA.
Mehdi FarokhniaNational Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0003-0902-4212
Lorenzo LeggioNational Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0001-7284-8754

Funding

All of Us Research Program Engagement and Retention InnovatorsOT2OD028395 · OD · RESEARCH TRIANGLE INSTITUTE · 2020 to 2025
$13.6M
NIAAA NIH HHSNIA NIH HHSNIDA NIH HHSNIH Office of the Director OT2OD028395
6 · The paper itself

Abstract

backgroundGrowing evidence suggests glucagon-like peptide-1 receptor agonists (GLP-1RAs) may represent a novel potential pharmacotherapeutic tool for alcohol use disorder (AUD). The objective of this study is to examine the association between GLP-1RA prescriptions and alcohol use.

methodsThis 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, a large program to recruit and collect surveys, EHR, genomic, and wearable data from a wide array of Americans. Among 15,447 participants with at least two recorded GLP-1RA prescriptions on separate days, we created three groups based on the timing of Alcohol Use Disorders Identification Test-Consumption (AUDIT-C) responses relative to first GLP-1RA prescription. This resulted in 3650 with current GLP-1RA prescriptions, 5642 with future GLP-1RAs (primary comparison group), and 544 with previous GLP-1RAs. AUDIT-C scores were compared across these groups and to propensity-score matched comparison groups.

resultsThose with current GLP-1RA prescriptions had statistically significant but modestly lower AUDIT-C scores compared with those with future prescriptions (incidence rate ratio [IRR] = 0.95; 95% CI: 0.91-0.99; p = 0.01). Participants with a previous 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 matched comparison group with the current GLP-1RA group (IRR = 0.89; 95% CI: 0.85-0.93; p ≤ 0.001) and no significant difference for the previous 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.

conclusionsThis 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.

Indexed as

Alcohol DrinkingAlcoholismGlucagon-Like Peptide-1 Receptor AgonistsAdultCohort StudiesCross-Sectional StudiesFemaleHumansMaleMiddle AgedUnited StatesGlucagon-Like Peptide-1 Receptor Agonistsalcohol consumptionall of usAUDIT‐Cglucagon‐like peptide‐1 receptor agonists

Identifiers

PMID42423024
PMCPMC13347274

What Socratic holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.