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The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
Sodium-Glucose Cotransporter-2 Inhibitors and Stroke Risk in Patients With Atrial Fibrillation
Ghee Kheng Lim1, Ramzi Ibrahim1, Xuan Ci Mee1
1Department of Cardiovascular Medicine, Mayo Clinic, Phoenix, Arizona, USA.
Insights
Sodium-glucose cotransporter 2 inhibitors (SGLT2-Is) significantly reduce stroke risk in patients with atrial fibrillation (AF). SGLT2-Is also lower risks for mortality, hospitalizations, and cardiac arrest in this population.
Area of Science:
- Cardiology
- Pharmacology
- Epidemiology
Background:
- Sodium-glucose cotransporter 2 inhibitors (SGLT2-Is) are established treatments for type 2 diabetes mellitus (T2DM) and heart failure (HF).
- The potential of SGLT2-Is to mitigate stroke risk in patients with atrial fibrillation (AF) is not well-established.
- This study investigates the effect of SGLT2-Is on stroke risk in patients diagnosed with AF.
Purpose of the Study:
- To evaluate the impact of SGLT2 inhibitors on stroke risk reduction in patients with atrial fibrillation.
- To assess the association of SGLT2 inhibitors with other cardiovascular and non-cardiovascular outcomes in AF patients.
Main Methods:
- A retrospective cohort study utilizing the TriNetX database.
- Inclusion criteria: patients aged 18 years or older with AF on anticoagulation.
- Propensity score matching (PSM) was employed to balance cohorts of SGLT2-Is users and non-users.
Main Results:
- The study included 152,778 patients (76,389 in each cohort) after PSM, with a mean age of 72.8 years.
- SGLT2-Is users demonstrated significantly lower risks of both ischemic stroke (aOR: 0.889) and hemorrhagic stroke (aOR: 0.682) compared to non-users.
- Secondary outcomes also showed reduced risks for SGLT2-Is users, including all-cause mortality (aOR: 0.615), hospitalizations (aOR: 0.599), AF cardioversion (aOR: 0.846), antiarrhythmic drug initiation (aOR: 0.790), and cardiac arrest (aOR: 0.643).
Conclusions:
- SGLT2 inhibitor use in patients with atrial fibrillation is linked to reduced risks of stroke.
- The findings suggest a broader benefit of SGLT2-Is, encompassing lower risks of mortality, hospitalizations, and cardiac arrest.
- Further prospective research is recommended to confirm these observational findings.
Background:
Sodium-glucose cotransporter 2 inhibitors (SGLT2-Is) are primarily used to manage type 2 diabetes mellitus (T2DM) and heart failure (HF), but their impact on reducing stroke risk in patients with atrial fibrillation (AF) remains underexplored. We aimed to investigate the impact of SGLT2-Is for stroke risk mitigation in patients with AF.
Methods:
Using the TriNetX database, we performed a retrospective cohort study on patients ≥ 18 years with AF and on anticoagulation. These patients were then classified into two cohorts based on their use of SGLT2-Is. To balance the baseline demographics, comorbidities, and medication use, propensity score matching (PSM) was used. The primary outcome was ischemic and hemorrhagic strokes, and the secondary outcomes were all-cause mortality, all-cause hospitalizations, need for AF cardioversion or antiarrhythmic drug initiation, and cardiac arrest. Adjusted odds ratio (aORs) and hazard ratios (HRs) were estimated for both the primary and secondary outcomes.
Results:
A total of 152,778 patients with 76,389 patients were included in each cohort (SGLT2-Is users, and non-users) after PSM. The mean age of both SGLT2-Is users and non-users was 72.8 years. For the SGLT2-Is users, the mean follow-up period was 317 days, whereas the mean follow-up period for the non-users was 306 days. For the primary outcome, we found that SGLT2-Is users had a lower risk of ischemic stroke (aOR: 0.889; 95% CI: 0.857-0.923) and hemorrhagic stroke (aOR: 0.682; 95% CI: 0.620-0.749) compared to non-users. Regarding the secondary outcomes, SGLT2-Is users also had lower risk for all-cause mortality (aOR: 0.615; 95% CI: 0.595-0.636), all-cause hospitalizations (aOR: 0.599; 95% CI: 0.587-0.611), need of AF cardioversion (aOR: 0.846; 95% CI: 0.813-0.881), antiarrhythmic drug initiation (aOR: 0.790; 95% CI: 0.766-0.815), and cardiac arrest (aOR: 0.643; 95% CI: 0.601-0.688).
Conclusions:
SGLT2-I use in patients with AF is associated with lower risks of stroke and other cardiovascular and non-cardiovascular outcomes. Future prospective research is needed to validate these findings.
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Secondary Active Transport
Glucose Transporters
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:

