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Published on: February 26, 2013
Effect of SLGT2 Inhibitors on Patients with Atrial Fibrillation
Justin Haloot1, Lucijana Krokar1, Auroa Badin1
1University of Texas Health San Antonio, San Antonio, TX.
Insights
Sodium glucose cotransporter 2 (SGLT2) inhibitors show reduced cardioversion and mortality risks in atrial fibrillation (AF) patients. However, SGLT2 inhibitors were linked to a higher risk of ischemic stroke in this population.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Sodium glucose cotransporter 2 (SGLT2) inhibitors are known for cardiovascular benefits.
- Limited data exists on SGLT2 inhibitors' impact on atrial fibrillation (AF) clinical outcomes.
Purpose of the Study:
- To compare ischemic stroke, acute coronary syndrome (ACS), cardioversion, and all-cause mortality in AF patients using SGLT2 inhibitors versus propensity-matched controls.
Main Methods:
- Retrospective study using a global medical research network database.
- Identified AF patients and those on SGLT2 inhibitors (dapagliflozin, empagliflozin, canagliflozin) for at least one month.
- Propensity matched 26,269 AF patients based on demographics, comorbidities, procedures, and medications.
Main Results:
- SGLT2 inhibitors associated with lower risk of cardioversion (HR 0.921) and all-cause mortality (HR 0.676).
- Increased risk observed for ischemic stroke (HR 1.081).
- No clear association found with acute coronary syndrome (ACS) events.
Conclusions:
- SGLT2 inhibitor use in AF patients correlates with reduced cardioversion and all-cause mortality.
- Kaplan-Meier analysis suggests a higher probability of survival with SGLT2 inhibitors in AF patients.
- Further research is needed to understand the increased ischemic stroke risk.
Background:
Sodium glucose cotransporter 2 (SGLT2) inhibitors have been associated with various cardiovascular benefits. There is limited data examining the effect of these medications on atrial fibrillation (AF) associated clinical outcomes. We compared ischemic stroke, acute coronary syndrome (ACS), cardioversion, and all-cause mortality outcomes in AF patients on SGLT2 inhibitors to propensity matched controls.
Materials And Methods:
We conducted a retrospective study with a global medical research network database. AF patients were identified via ICD codes that must have been present for at least one month. Patients on SGLT2 inhibitors were identified as those on dapagliflozin, empagliflozin, or canagliflozin for at least one month. AF patients on SGLT2 inhibitors were propensity matched to those not on SGLT2 inhibitors based on age, race, ethnicity, cardiovascular comorbidities, valvular disease, pulmonary disease, urinary diseases, cardiovascular procedures, cardiovascular medications, and anticoagulants. We examined incidence of ischemic stroke, at least one ACS episode, cardioversion, and all-cause mortality.
Results:
In 26,269 AF patients, SGLT2 inhibitors were associated with lower risk of cardioversion (HR 0.921, 95% CI 0.841 - 0.999, p = 0.0245) and all-cause mortality (HR 0.676, 95% CI 0.635 - 0.721, p < 0.0001). However, there was an association with increased risk for ischemic stroke (HR 1.081, 95% CI 1.012 - 1.154, p 0.0201). There was no clear association with ACS events.
Conclusions:
In patients with AF, use of SGLT2 inhibitors was associated with a lower risk of cardioversion and all-cause mortality and higher probability of survival based on Kaplan-Meier analysis.
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