Do Glucagon-like peptide-1 (GLP-1) analogs work for treating addiction?

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Last updated: June 19, 2025View editorial policy

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From the Guidelines

GLP-1 analogs are not yet FDA-approved for treating addiction, and their use for this purpose is still being researched. While medications like semaglutide and liraglutide have shown promise in reducing cravings and substance use by affecting reward pathways in the brain, the current evidence is limited to early research studies 1. The mechanism of GLP-1 analogs in treating addiction appears to involve modulation of dopamine signaling in the mesolimbic reward system, which is common to both food intake and addictive behaviors.

Some key points to consider when evaluating the potential of GLP-1 analogs for addiction treatment include:

  • The lack of standardized dosing protocols or treatment guidelines for using GLP-1 analogs off-label for addiction treatment
  • The need for further research to fully understand the efficacy and safety of GLP-1 analogs for this purpose
  • The importance of consulting with addiction medicine specialists or psychiatrists familiar with emerging GLP-1 research for patients interested in this approach
  • The continued use of traditional evidence-based treatments for addiction, including FDA-approved medications, behavioral therapies, and support groups, as the first-line approaches while research on GLP-1 analogs continues to develop.

It is essential to prioritize traditional evidence-based treatments for addiction and to approach the use of GLP-1 analogs with caution, considering the limited current evidence and the potential risks and benefits of this treatment approach 1.

From the Research

GLP-1 Analogs and Addiction Treatment

  • GLP-1 analogs have shown potential in treating addiction, with studies suggesting they may reduce alcohol and substance use disorders (ASUDs) 2, 3, 4, 5, 6.
  • The exact mechanisms underlying the impact of GLP-1R agonists on addiction are not fully understood, but proposed mechanisms include reward processing, stress, and cognitive function, as well as broader mechanisms related to satiety, changes in gastric motility, and glucose homeostasis 2, 3, 6.

Preclinical Evidence

  • Preclinical studies have demonstrated that GLP-1R agonists reduce alcohol and substance use in animal models, with effects observed on binge-like drinking, operant self-administration, and dependence-induced drinking 3, 4.
  • GLP-1R agonists have also been shown to modulate central GABA neurotransmission, which may contribute to their anti-addictive effects 4.

Clinical Evidence

  • Clinical studies on the use of GLP-1R agonists for addiction treatment are limited, but suggest that these medications may be safe and effective in reducing ASUDs 2, 3, 5.
  • A systematic review of randomized trials found that GLP-1R agonists significantly decreased substance use disorder (SUD) in patients, with notable reductions in body weight, BMI, and HbA1c also observed 5.

Future Directions

  • Further research is needed to fully understand the mechanisms of action of GLP-1R agonists in addiction treatment and to identify preferred compounds and patient subgroups who may benefit most from these medications 2, 6.
  • Ongoing clinical trials will help to determine the efficacy and safety of GLP-1R agonists for addiction treatment, with potential implications for the development of new therapies for ASUDs 2, 5.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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