# Effect of liraglutide on depressive symptoms in overweight or obese patients with type 2 diabetes: protocol for a pilot randomized controlled trial

**Authors:** Wei Fang, Zinan Li, Jie Xu, Jing Zhao, Hongxia Zhu, Huanping Wang

PMC · DOI: 10.3389/fendo.2025.1629157 · Frontiers in Endocrinology · 2026-01-21

## TL;DR

This study tests if liraglutide, a diabetes drug, can also help reduce depression in overweight or obese patients with type 2 diabetes.

## Contribution

This is the first pilot trial to investigate liraglutide's antidepressant effects in patients with obesity, diabetes, and depression.

## Key findings

- Liraglutide's effects on depression will be evaluated alongside glucose control and weight changes.
- The study will use brain imaging and biomarkers to explore liraglutide's antidepressant mechanisms.
- Results may guide future large-scale trials on treating depression in diabetic patients.

## Abstract

Patients with concurrent obesity, type 2 diabetes, and depression experience high disease severity and prevalence. This triad of conditions compromises quality of life and treatment adherence, further exacerbating disease progression. Therapeutic strategies for such patients must address both glycemic control and psychological well-being. Liraglutide, a glucagon-like peptide-1 receptor agonist (GLP-1RA), offers benefits beyond glucose-lowering and weight reduction, with emerging evidence suggesting it may also alleviate depressive symptoms. Therefore, liraglutide represents a promising intervention for managing depression in patients with obesity and diabetes.

This study aims to assess the therapeutic efficacy of liraglutide in overweight or obese patients with type 2 diabetes and comorbid depression, with a specific focus on its antidepressant effects.

This is a randomized, double-blind, placebo-controlled pilot trial. Sixty eligible participants will be randomly assigned (1:1) to receive either liraglutide (initiated at 0.6 mg/day, titrated weekly to a maximum of 1.8 mg/day) or a matched placebo, as an adjunct to standard care for 12 weeks. The primary endpoints include blood glucose levels, glycated hemoglobin, body mass index, Hamilton Depression Rating Scale score, and metrics derived from resting-state functional magnetic resonance imaging (resting-state fMRI). Secondary endpoints will assess changes in inflammatory biomarkers (tumor necrosis factor-α, interleukin-6), oxidative stress indicators (superoxide dismutase, malondialdehyde), homeostasis model assessment of insulin resistance, insulin sensitivity index, and homeostasis model assessment of β-cell function.

This trial will provide preliminary data on the effects of liraglutide on depressive symptoms in overweight/obese patients with type 2 diabetes. The findings are expected to provide a basis and reference for subsequent large-scale clinical research.

## Linked entities

- **Chemicals:** liraglutide (PubChem CID 16134956), malondialdehyde (PubChem CID 10964)
- **Diseases:** type 2 diabetes (MONDO:0005148), depression (MONDO:0002050), obesity (MONDO:0011122)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** type 2 diabetes (MESH:D003924), obese (MESH:D009765), inflammatory (MESH:D007249), Depression (MESH:D003866), insulin resistance (MESH:D007333), diabetes (MESH:D003920), weight (MESH:D015431), overweight (MESH:D050177)
- **Chemicals:** glucose (MESH:D005947), blood glucose (MESH:D001786), malondialdehyde (MESH:D008315)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12867914/full.md

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Source: https://tomesphere.com/paper/PMC12867914