# The role of dulaglutide in the treatment of alcohol use disorder: a case report

**Authors:** Olivia Hill, Sarah Hughes, Aakanksha Singh, Michael Ang-Rabanes, Raja Mogallapu

PMC · DOI: 10.3389/fpsyt.2025.1420316 · Frontiers in Psychiatry · 2025-05-01

## TL;DR

This case report shows that dulaglutide, a diabetes medication, may help reduce alcohol use and cravings in a patient with alcohol use disorder.

## Contribution

The paper presents a novel case report suggesting dulaglutide's potential as a treatment for Alcohol Use Disorder.

## Key findings

- The patient experienced reduced alcohol cravings and consumption while on dulaglutide.
- Discontinuation of dulaglutide led to a return to previous drinking patterns.
- Dulaglutide also contributed to weight loss in the patient.

## Abstract

Glucagon-like peptide 1 (GLP-1) receptor agonists, medications commonly employed in the treatment of type 2 diabetes mellitus, have illustrated several additional benefits, including weight loss and potentially reduce addictive cravings. Several studies have indicated that GLP-1 receptor agonists may be effective in treating Alcohol Use Disorder (AUD), for which current pharmacologic therapies are often inadequate. Proposed mechanisms include modulation of dopaminergic transmission and reduced gastric emptying, both of which reduce alcohol craving and tolerance. This case report discusses dulaglutide’s ability to reduce alcohol consumption. During a visit to an outpatient behavioral health clinic, a 44-year-old male was evaluated for weight loss. His medical history revealed a BMI of 41.8, hypertension, major depressive disorder, and pre-diabetes. The individual also reported the consumption of approximately ninety beers per month and was in the pre-contemplation phase of change. As part of the treatment plan, the patient was prescribed dulaglutide to manage pre-diabetes and facilitate weight loss. During subsequent appointments, the individual not only experienced weight loss but also noted a substantial reduction in alcohol cravings and consumption. However, following a lapse in insurance coverage the following year, the individual had to discontinue his dulaglutide, resulting in a return to previous drinking patterns. Future research should focus on confirming existing animal study results in humans, with the hope that GLP-1 receptor agonists can become a mainstay treatment for AUD.

## Linked entities

- **Diseases:** type 2 diabetes mellitus (MONDO:0005148), major depressive disorder (MONDO:0002009), pre-diabetes (MONDO:0006920)

## Full-text entities

- **Genes:** Glp1r (glucagon-like peptide 1 receptor) [NCBI Gene 14652] {aka GLP-1R, GLP1Rc}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, Gcg (glucagon) [NCBI Gene 14526] {aka GLP-1, Glu, PPG}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** AUD (MESH:D000437), type 2 diabetes (MESH:D003924), obesity (MESH:D009765), substance use disorder (MESH:D019966), Insulin resistance (MESH:D007333), liver disease (MESH:D008107), pre (MESH:D058246), seizures (MESH:D012640), binge eating (MESH:D002032), Binge eating and substance use disorders (MESH:D056912), craving (MESH:C564883), binge drinking (MESH:D063425), word-finding difficulty (MESH:D009461), back injury (MESH:D019567), diabetes (MESH:D003920), depression (MESH:D003866), weight gain (MESH:D015430), hypertension (MESH:D006973), weight loss (MESH:D015431), renal disease (MESH:D007674), prediabetes (MESH:D011236), deaths (MESH:D003643)
- **Chemicals:** blood sugar (MESH:D001786), acamprosate (MESH:D000077443), naltrexone (MESH:D009271), lipid (MESH:D008055), acetaldehyde (MESH:D000079), dopamine (MESH:D004298), triglyceride (MESH:D014280), Exendin-4 (MESH:D000077270), phentermine (MESH:D010645), Wellbutrin (MESH:D016642), ethanol (MESH:D000431), hydrochlorothiazide (MESH:D006852), topiramate (MESH:D000077236), glucose (MESH:D005947), Disulfiram (MESH:D004221), alcohol (MESH:D000438)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Mutations:** R 168Ser, 168Ser

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12078295/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC12078295/full.md

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Source: https://tomesphere.com/paper/PMC12078295