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Abstract Number: 2657

Incidence of Rheumatic Diseases Among Patients Receiving GLP-1 Receptor Agonists: A Comparative Analysis with DPP-4 Inhibitors in a Propensity Score-Matched Cohort

Betul Ibis1, Furkan Bahar1, Yu-Che Lee2, Ko-Yun Chang3, Yu Chang4 and Cho-Han Chiang5, 1Mount Auburn Hospital, Harvard Medical School, Cambridge, MA, 2University at Buffalo, Buffalo, NY, 3National Jewish Health, Denver, CO, 4National Cheng Kung University Hospital, Tainan, Taiwan (Republic of China), 5Mount Auburn Hospital, Harvard Medical School, Cambridge

Meeting: ACR Convergence 2025

Keywords: Cohort Study, Epidemiology

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Session Information

Date: Wednesday, October 29, 2025

Title: Abstracts: Epidemiology & Public Health I (2657–2662)

Session Type: Abstract Session

Session Time: 11:30AM-11:45AM

Background/Purpose: GLP-1 receptor agonists (GLP-1RAs) are increasingly utilized in diabetes mellitus management due to their glucose-lowering and cardiovascular benefits. However, the effect of GLP-1RAs on rheumatic disease incidence is not well defined. This study evaluates the incidence of rheumatic diseases in patients treated with GLP-1RAs, using patients receiving DPP-4 inhibitors (DPP-4i) as a comparator group.

Methods: We conducted a propensity score-matched cohort study utilizing the TriNetX Analytics Network database, comprising anonymized patient data from healthcare institutions worldwide. Adult patients (≥18 years) initiating treatment with GLP-1RAs were matched 1:1 with those initiating DPP-4i therapy based on age, sex, race, hemoglobin A1c levels, BMI, underlying comorbidities, commonly used medications, and diabetes medications to ensure baseline comparability. The primary outcomes included the incidence rates of rheumatoid arthritis, gout, systemic lupus erythematosus, ankylosing spondylitis, scleroderma, psoriatic arthritis, and osteoarthritis within 1 year after the index date. Cox proportional hazards models were employed to assess and compare the risk (hazard ratios [HRs]) of developing various rheumatic diseases between the groups. Statistical significance was set at a p-value < 0.05.

Results: After matching, each group comprised 217,302 patients. Mean age (59.5±12.5 vs. 59.6±13.3 years), sex (50.9% vs. 51.2% males), mean hemoglobin A1c (8.4 ± 2.0 vs. 8.4 ± 2.1), and BMI (33.5 ± 7.6 vs. 32.7 ± 7.3) were similar between groups. Additionally, the GLP-1RA group showed significantly reduced risks of rheumatoid arthritis (HR 0.87; 95% CI 0.77–0.98; p=0.026), gout (HR 0.82; 95% CI 0.77–0.88; p< 0.001), and osteoarthritis (HR 0.92; 95% CI 0.89–0.94; p< 0.001). No significant differences were noted for systemic lupus erythematosus, ankylosing spondylitis, scleroderma, or psoriatic arthritis.

Conclusion: In this propensity score-matched study, GLP-1RA therapy was associated with a significantly reduced incidence of rheumatoid arthritis, gout, osteoarthritis, compared to DPP-4i treatment. These findings suggest beneficial effects of GLP-1RAs on rheumatological outcomes, supporting their broader therapeutic implications in diabetes management.

Supporting image 1Table 1. Patient baseline characteristics before and after propensity score matching

Supporting image 2Table 2. Incidence of rheumatic diseases among patients with GLP-1RA vs DPP-4i group


Disclosures: B. Ibis: None; F. Bahar: None; Y. Lee: None; K. Chang: None; Y. Chang: None; C. Chiang: None.

To cite this abstract in AMA style:

Ibis B, Bahar F, Lee Y, Chang K, Chang Y, Chiang C. Incidence of Rheumatic Diseases Among Patients Receiving GLP-1 Receptor Agonists: A Comparative Analysis with DPP-4 Inhibitors in a Propensity Score-Matched Cohort [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/incidence-of-rheumatic-diseases-among-patients-receiving-glp-1-receptor-agonists-a-comparative-analysis-with-dpp-4-inhibitors-in-a-propensity-score-matched-cohort/. Accessed .
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All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

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