Evaluating the Risk of Autoimmune Disorders Associated with GLP-1 Receptor Agonists, DPP-4 Inhibitors, and SGLT2 Inhibitors in Diabetic Patients
By
Arjun Mahajan
David W. Bates
Alessandro Doria
Dinah Foer
Avery H. LaChance
Jeffrey A. Sparks
July 1, 2026
Objective: To systematically compare the risk of autoimmune diseases among patients with type 2 diabetes treated with DPP-4 inhibitors, GLP-1 receptor agonists, and SGLT2 inhibitors.
Approach: Outcomes: Primary outcomes included incidences of systemic lupus erythematosus, cutaneous lupus erythematosus, rheumatoid arthritis, psoriasis, psoriatic arthritis, multiple sclerosis, inflammatory bowel disease, antineutrophilic cytoplasmic antibody-associated vasculitis, giant cell arteritis, dermatomyositis, systemic sclerosis, celiac disease, autoimmune thyroiditis, myasthenia gravis, pemphigus, bullous pemphigoid, polymyositis, and polymyalgia rheumatica.Key Findings: Thesudyincl1849maprofG0256vk Interpretation: The study evaluates the association of commonly used antidiabetic agents with autoimmune diseases.
Limitations: The study is observational and may be subject to residual confounding. Data sharing restrictions prevent public access to individual-level data. The observational design limits the ability to establish causality. Conclusion: The study aims to enhance understanding of the autoimmune disease risk associated with different diabetes medications.