Abstract 4359705: Glucagon-like Peptide-1 Receptor Agonists and Sodium-Glucose Cotransporter-2 Inhibitors Reduce Dementia Risk in Type 2 Diabetes: A Comprehensive Bayesian Network Meta-Analysis
Abstract
Background: Glucagon-like peptide-1 receptor agonists (GLP-1RAs) and sodium-glucose cotransporter-2 inhibitors (SGLT2is) are cardioprotective glucose-lowering therapies, but their impact on dementia risk in type 2 diabetes remains underexplored. Methods: We searched PubMed, Scopus, and Embase from inception to May 1, 2025, for randomized controlled trials (RCTs) comparing GLP-1RAs or SGLT2is with controls, reporting dementia or cognitive score changes. Included trials featured guideline-recommended drugs for cardiovascular risk reduction. A Bayesian network meta-analysis estimated risk ratios (RR) with 95% credible intervals (CrI) using Markov Chain Monte Carlo methods, with Gelman-Rubin diagnostics for convergence. Surface under the cumulative ranking curve (SUCRA) ranked treatments. Results: From 22 RCTs with 156,697 patients, therapies showed varied dementia risk reductions. For all-cause dementia versus control according to the SUCRA: albiglutide (RR: 0.03, 95% CrI: 0.00 to 0.08; SUCRA: 94.4%), lixisenatide (RR: 0.08, 95% CrI: 0.00 to 0.20; SUCRA: 93.62%), efpeglenatide (RR: 0.24, 95% CrI: 0.00 to 1.38; SUCRA: 70.09%), canagliflozin (RR: 0.31, 95% CrI: 0.01 to 1.47; SUCRA: 61.81%), semaglutide (RR: 0.50, 95% CrI: 0.03 to 1.98; SUCRA: 50.06%), liraglutide (RR: 2.12, 95% CrI: 0.02 to 9.89; SUCRA: 41.91%), empagliflozin (RR: 0.68, 95% CrI: 0.05 to 2.35; SUCRA: 39.63%), exenatide (RR: 4.13, 95% CrI: 0.02 to 20.28; SUCRA: 35.41%), dulaglutide (RR: 3.38, 95% CrI: 0.03 to 15.72; SUCRA: 32.89%), dapagliflozin (RR: 1.19, 95% CrI: 0.09 to 4.96; SUCRA: 30.37%), ertugliflozin (RR: 6.79, 95% CrI: 0.02 to 29.23; SUCRA: 30.1%), control (SUCRA: 19.67%). For vascular dementia versus control: dapagliflozin (RR: 0.01, 95% CrI: 0.00 to 0.08; SUCRA: 86.65%), ertugliflozin (RR: 0.03, 95% CrI: 0.00 to 0.16; SUCRA: 85.98%), dulaglutide (RR: 0.05, 95% CrI: 0.00 to 0.32; SUCRA: 84.35%), while semaglutide (RR: 3.83, 95% CrI: 0.05 to 21.72; SUCRA: 17.4%), and control (SUCRA: 13.2%). For Alzheimer’s dementia versus control: dulaglutide showed the lowest (RR: 0.87, 95% CrI: 0.01 to 4.68; SUCRA: 77.64%), while exenatide the highest (RR: 60.62, 95% CrI: 0.21 to 185.09; SUCRA: 23.36%), and control (SUCRA: 50.29%). Conclusions: GLP-1RAs and SGLT2is reduce dementia risk, with albiglutide and lixisenatide excelling for all-cause dementia, dapagliflozin and ertugliflozin for vascular dementia, and dulaglutide for Alzheimer’s. Higher risks with some drugs highlight tailored therapy needs.
Article Details
Authors (6)
Ibrahim Khalil
Dhaka Medical College and Hospital, Dhaka, Bangladesh
Md. Imran Hossain
Mst. Mahmuda Akter
Manikganj Medical College, Manikganj, Bangladesh
Mohd Turzo Rahman
Flushing Hospital Medical Center, Flushing, New York, United States
Sajjad Ghanim Al-Badri
College of Medicine, University of Baghdad, Baghdad, Iraq
Sunjida Amin Promi
Chittagong Medical College, Chittagong, Bangladesh