# Emerging therapeutic potential of glucagon-like Peptide-1 receptor agonists in knee osteoarthritis: a systematic review

**Authors:** Yapeng Li, Lanbo Yang, Feng Li, Jia Fu, Wangyu Zhao, Xiaolong Wu, Jiayi Guo, Chen Yue

PMC · DOI: 10.3389/fphar.2025.1627691 · 2025-10-13

## TL;DR

This paper reviews how GLP-1 receptor agonists may help treat knee osteoarthritis by reducing pain and inflammation, especially in obese or diabetic patients.

## Contribution

The study systematically reviews GLP-1 RAs as a novel therapeutic approach for knee osteoarthritis, highlighting their metabolic and anti-inflammatory mechanisms.

## Key findings

- GLP-1 RAs improved pain and function in knee osteoarthritis patients.
- Mechanisms include metabolic regulation, anti-inflammatory effects, and cartilage preservation.
- Safety concerns include gastrointestinal issues and potential tumor risks.

## Abstract

This study aims to systematically investigate the clinical efficacy and mechanisms of glucagon-like peptide-1 (GLP-1) receptor agonists (GLP-1 RAs) in the treatment of knee osteoarthritis (KOA), elucidate their underlying mechanisms, and propose potential future research directions.

This study followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. We reviewed literature from PubMed, Embase, Web of Science, Cochrane Library, and ClinicalTrials.gov up to 31 December 2024. The search strategy combined “GLP-1″ and “KOA”. We included studies on GLP-1 RAs and KOA in humans and animals, excluding conference abstracts, reviews, letters, case reports, and other similar types of publications.

Fifteen studies were included, covering six clinical investigations and nine fundamental research studies. Clinical evidence showed GLP-1 RAs significantly improved pain scores and function while reducing KOA incidence. Mechanistic studies reveal multi-target effects, including: 1) Metabolic regulation, 2) Anti-inflammatory action, and 3) Cartilage preservation through autophagy activation and apoptosis inhibition. Safety analysis notes gastrointestinal and tumor events. At the same time, we are concerned about a declining trend in long-term compliance with GLP-1 RAs.

These findings positioned GLP-1 RAs as promising disease-modifying agents for metabolic-associated KOA, particularly in obese or diabetic subpopulations. While current evidence supports therapeutic potential, confirmatory phase III trials and long-term safety monitoring are needed to establish clinical guidelines.

https://www.crd.york.ac.uk/PROSPERO2/view/CRD420250656321, Identifier, CRD420250656321.

## Linked entities

- **Diseases:** obesity (MONDO:0011122), diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}
- **Diseases:** pain (MESH:D010146), KOA (MESH:D020370), inflammatory (MESH:D007249), obese (MESH:D009765), diabetic (MESH:D003920), gastrointestinal and tumor (MESH:D005770)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12554640/full.md

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Source: https://tomesphere.com/paper/PMC12554640