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Updated: Sep 14, 2025

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Published on: February 26, 2013
Association of Glucagon-Like Peptide-1 Receptor Agonist with Incident Atrial Fibrillation
Suzan Khalil1,2, William Hicks1,2, Floyd W Burke3
1University of Central Florida/HCA Florida Healthcare, Greater Orlando, FL, USA.
Background:
Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have shown efficacy in reducing cardiovascular events in patients with diabetes mellitus (DM), but conflicting evidence exists regarding their impact on cardiac arrhythmias. Whereas some studies associated GLP-1RAs with arrhythmogenesis, other studies suggested a decreased association with atrial fibrillation (AF).
Objective:
The aim was to compare the risk of incident AF after initiation of GLP-1RAs versus dipeptidyl peptidase-4 inhibitors (DPP4is), as active comparators, in patients with DM.
Design:
A retrospective propensity score-matched cohort study was conducted.
Setting:
The national data of Veterans Health Administration during fiscal years 2006-2021 were used for the study.
Patients:
Adults who initiated either GLP-1RA or DPP4i medications were included.
Measurements:
The primary outcome was a composite outcome of AF (diagnosis of AF/flutter or undergoing an AF procedure).
Results:
Out of 116,235 GLP-1RA users and 217,668 DPP4i users, we propensity score-matched 80,948 pairs, on 88 characteristics. The composite outcome of AF was similar in the GLP-1RA group (4.1%) and DPP4i group (4.3%); odds ratio (OR) 0.96, 95% confidence interval (CI) 0.92-1.01. Secondary analyses stratified by medication use duration showed no significant differences in composite AF risk (p > 0.05). Individuals achieving 5% weight loss from baseline body weight had significantly lower AF incidence (OR 0.83, 95% CI 0.78-0.89), whereas no significant differences were observed in those with no weight loss or weight gain (OR 1.05, 95% CI 0.97-1.12).
Conclusions:
GLP-1RA use was not associated with a decreased or increased risk of AF compared to DPP4i use. In subgroup analysis, lower AF risk was seen in GLP-1RA versus DPP4i users who achieved weight loss, which suggests weight loss as a potential modifier of response to GLP-1RAs.
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