Can Glucagon-like peptide-1 (GLP-1) receptor agonists, such as liraglutide (Victoza) or semaglutide (Ozempic), be used to manage depression in patients with type 2 diabetes?

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Last updated: June 27, 2025View editorial policy

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From the Guidelines

GLP-1 receptor agonists, such as liraglutide and semaglutide, can be considered as a potential adjunctive treatment for managing depression in patients with type 2 diabetes, as they have been shown to improve depressive symptoms in this population 1.

Key Points to Consider

  • The primary indication for GLP-1 receptor agonists remains glycemic control and cardiovascular risk reduction in type 2 diabetes.
  • Emerging evidence suggests that GLP-1 receptor agonists may have a positive effect on depressive symptoms, possibly through improved metabolic health or anti-inflammatory mechanisms.
  • A systematic review and meta-analysis found that the use of GLP-1 receptor agonists led to significant improvement in depressive symptoms among adults with type 2 diabetes 1.
  • Patients with type 2 diabetes experiencing depression should still receive standard depression treatments, including psychotherapy and/or antidepressant medications, as GLP-1 receptor agonists are not a replacement for these therapies.
  • Healthcare providers should discuss comprehensive treatment options with their patients, considering the potential benefits of GLP-1 receptor agonists on both glycemic control and depressive symptoms.

Important Considerations

  • The evidence for the use of GLP-1 receptor agonists in managing depression is still evolving and primarily based on their effects on glycemic control and cardiovascular risk reduction.
  • Other treatments, such as lifestyle interventions (e.g., changing nutrition and/or physical activity) and psychological interventions (e.g., cognitive behavioral therapy), have also demonstrated benefits for depressive symptoms and should be considered as part of a comprehensive treatment plan 1.

From the Research

GLP-1 Receptor Agonists and Depression

  • GLP-1 receptor agonists, such as liraglutide and semaglutide, are commonly used to manage type 2 diabetes and have been shown to have potential effects on mental health, including depression 2, 3, 4.
  • Some studies suggest that GLP-1 receptor agonists may have neuroprotective and antidepressant properties, although the evidence is mixed and more research is needed to fully understand their effects on depression 3, 5, 6.

Case Reports and Observational Studies

  • Case reports have described instances of depression associated with the use of GLP-1 receptor agonists, such as semaglutide and liraglutide, in patients with type 2 diabetes 2, 4.
  • Observational studies have found mixed results regarding the potential of GLP-1 receptor agonists to lower the risk of incident depression in patients with diabetes mellitus, with some studies suggesting a significant reduction in risk and others showing no effect 3.

Mechanisms and Potential Therapeutic Effects

  • GLP-1 receptor agonists may exert their effects on depression through various mechanisms, including modulation of glucose fluctuations, dopamine regulation, and influence on the brain reward system 4, 5.
  • Some studies have suggested that GLP-1 receptor agonists, such as liraglutide, may have therapeutic potential in the treatment of depression, particularly in patients with comorbid metabolic disorders 5, 6.

Limitations and Future Directions

  • The current evidence is limited by the small number of studies and the lack of controlled trials, highlighting the need for further research to fully understand the effects of GLP-1 receptor agonists on depression 3, 4.
  • Future studies should aim to investigate the neuroprotective potential of different classes and doses of GLP-1 receptor agonists using controlled trials and explore their potential therapeutic applications in the treatment of depression 3, 6.

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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