Key result
SGLT2 inhibitors linked to ~11 ms reduction in total atrial conduction time in T2D.
Why the study?
The effect of SGLT2 inhibitors on echocardiography-derived total atrial conduction time, a marker of atrial remodeling in type 2 diabetes mellitus, remains unclear.
Does SGLT2 inhibitor therapy reduce echocardiography-derived total atrial conduction time in patients with type 2 diabetes mellitus?
Observational (n=107)
No
Does SGLT2 inhibitor therapy reduce echocardiography-derived total atrial conduction time in patients with type 2 diabetes mellitus?
In patients with type 2 diabetes mellitus, 6 months of SGLT2 inhibitor therapy was associated with a significant reduction in echocardiography-derived total atrial conduction time, suggesting potential improvement in atrial structural and electrical remodeling.
SGLT2 inhibitor use was associated with shorter atrial conduction time in T2DM with preserved EF; hypothesis-generating and requires randomized confirmation before practice change.
Background: Sodium-glucose cotransporter 2 inhibitors (SGLT2i) have been shown to improve cardiovascular outcomes in patients with type 2 diabetes mellitus (T2DM). Structural and electrical atrial remodeling are among the myocardial alterations associated with diabetes. Total atrial conduction time (TACT), derived from echocardiography, serves as a marker of atrial remodeling. However, the effect of SGLT2i on TACT remains unclear. Methods: In this prospective, single-center pilot study, 130 patients with T2DM and preserved left ventricular ejection fraction were enrolled between March and December 2022. After excluding patients who discontinued therapy or met other exclusion criteria, 107 patients (57 treated with dapagliflozin and 50 with empagliflozin) were included in the analysis. Echocardiographic and laboratory evaluations were performed at baseline and six months after initiation of SGLT2i therapy. TACT was defined as the mean time between the onset of the P wave in lead II and the peak A' wave on tissue Doppler imaging (PA-TDI). Paired statistical tests, correlation analyses, and multiple linear regression were used to identify independent predictors of Δ TACT. Results: = 0.026, respectively). The mean duration of SGLT2i use was 183 days. Conclusions: SGLT2i therapy was associated with a significant reduction in TACT among T2DM patients, suggesting potential improvements in atrial remodeling and diastolic function. These findings support the hypothesis that the cardiovascular benefits of SGLT2i may extend to atrial conduction properties. Nonetheless, larger randomized studies are warranted to confirm these observations.
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Taştan et al. (2026) conducted an observational in Type 2 diabetes mellitus (n=107). Sodium-glucose cotransporter 2 inhibitors (SGLT2i) vs. Baseline (Pre-treatment) was evaluated on Mean total atrial conduction time (TACT) derived from PA-TDI duration (p=< 0.001). Six months of SGLT2 inhibitor therapy significantly reduced echocardiography-derived total atrial conduction time from a median of 121.1 ms at baseline to 110.5 ms in patients with type 2 diabetes and preserved ejection fraction.
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