EClinicalMedicine

Link between using glucagon-like peptide-1 receptor agonists and changes in alcohol drinking

Updated

Abstract

Among 88,190 participants, 43.9% received glucagon-like peptide-1 receptor agonists (GLP-1 RAs).

  • Randomized controlled trials (RCTs) did not show a reduction in alcohol consumption after 24 weeks of treatment with exenatide compared to placebo.
  • A subgroup analysis indicated a positive effect on alcohol consumption in individuals with obesity (BMI >30 kg/m).
  • Participants taking dulaglutide were 29% more likely to reduce alcohol intake compared to those on placebo.
  • Observational studies reported fewer alcohol-related healthcare events with GLP-1 RAs treatment compared to no treatment and other medications.
  • There is limited high-quality evidence on the effects of GLP-1 RAs on alcohol use, necessitating further research.

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Funding

Competing interests

All authors have submitted the ICMJE COI form. Authors (MS, JK, FCW, SC, SE, SB, JG, NB) declare no conflict of interest. Authors (AD, MJD, PAG, RB, SK, GPA) have declared the following conflicts of interest. AD: Received grants or contracts from ARMS-Hub study (NIHR PHR) and BOOST trial (NIHR RfPB). Participates in the NIHR BASIS trial Drug Monitoring Committee. MJD: Received grants or contracts from AstraZeneca, Novo Nordisk, Boehringer Ingelheim, Janssen, Sanofi-Aventis, and Eli Lilly. Consulting fees from Lilly, Boehringer Ingelheim, Novo Nordisk, and Sanofi. Honoraria for lectures and presentations from Boehringer Ingelheim, Lilly, Novo Nordisk, Sanofi, and AstraZeneca. Participates in Data Safety Monitoring Boards for Boehringer Ingelheim, Eli Lilly, Novo Nordisk, Sanofi, Carmot, Zealand Pharma, Pfizer, Medtronic, and AstraZeneca. PAG: Received grants or contracts from EPSRC, BBSRC, MRC, Wellcome Leap, and NIHR. Honoraria for lectures from the International Society for Magnetic Resonance in Medicine (ISMRM). Holds leadership roles as Secretary of ISMRM and Councillor for Nottinghamshire County Council and Rushcliffe Borough Council. Received equipment or services from ASG and Philips. RB: Consulting fees from GSK, Novonordisk, and Boehringer Ingelheim. Honoraria for lectures from Gilead and Abbvie. SK: Received grants from UK NIHR for the MHIN Grant Alcohol Assertive Outreach Study, MAHSC Grant for Early Detection in Liver Fibrosis Study, and EME Grant for the MORE-KARE Study. Honoraria for a presentation to the British Association of Psychopharmacology. GPA: Received grants from NIHR, EU DILI consortium, and Gilead. Consulting fees through the Nottingham University Consultants team.
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