Key result
Dapagliflozin initiation linked to greater ventricular repolarization marker reductions, most pronounced in HFrEF.
Why the study?
T2DM is associated with abnormal ventricular repolarization and increased arrhythmic risk, and the electrophysiological effects of SGLT-2 inhibitors beyond glycemic control are unclear.
Does dapagliflozin improve surrogate ECG markers of ventricular repolarization at 3 months in SGLT-2 inhibitor-naïve patients with T2DM across different heart failure phenotypes?
Observational (n=700)
Does dapagliflozin improve surrogate ECG markers of ventricular repolarization at 3 months in SGLT-2 inhibitor-naïve patients with T2DM across different heart failure phenotypes?
Effect estimate: Cohen's d 0.48-1.08
p-value: p=<0.001
Initiation of dapagliflozin in patients with Type 2 diabetes significantly improved surrogate ECG markers of ventricular repolarization, with the most pronounced effects observed in patients with HFrEF.
Hypothesis-generating for arrhythmic risk reduction with dapagliflozin in T2DM-HF; should not yet change practice.
Background Type 2 diabetes mellitus (T2DM) is associated with abnormal ventricular repolarization and increased arrhythmic risk. Sodium-glucose cotransporter-2 (SGLT-2) inhibitors may exert electrophysiological effects beyond glycemic control. We investigated changes in electrocardiographic (ECG) markers of ventricular repolarization after dapagliflozin initiation in SGLT-2 inhibitor-naïve patients with T2DM according to heart failure (HF) phenotype.Methods In this prospective, non-randomized, controlled observational study, 700 patients with T2DM were enrolled between June 2023 and February 2026. Patients initiating dapagliflozin (n = 350) were classified as HFrEF (LVEF <50%, n = 87), HFpEF (LVEF ≥50% with HF, n = 93), or no HF (LVEF ≥50% without HF, n = 170); 350 controls continued pre-existing antidiabetic therapy. Twelve-lead ECG and echocardiography were performed at baseline and 3 months. Prespecified endpoints included QT, QTc, QT dispersion, Tp-e, Tp-e/QT, and Tp-e/QTc. Inverse probability of treatment weighting and Holm-Bonferroni correction were applied.Results Dapagliflozin was associated with greater reductions in all prespecified ECG parameters than controls (all between-group p <0.001; Cohen’s d = 0.48–1.08), with consistent findings after IPTW. Reductions were greatest in HFrEF (QTc = −14.3 ms; Tp-e = −9.1 ms), followed by HFpEF (−11.2 and −7.4 ms) and no HF (−7.6 and −3.8 ms); all between-subgroup comparisons p <0.001. HFrEF independently predicted greater QTc reduction (β = −4.8 ms vs no HF, p < 0.001). Change in Tp-e correlated weakly with HbA1c change (r = −0.145, p = 0.037). LVEF increased in HFrEF (+3.2%) and HFpEF (+0.9%).Conclusions Dapagliflozin initiation was associated with reductions in multiple ECG markers of ventricular repolarization, with the greatest changes observed in HFrEF. These findings concern surrogate ECG measures and do not establish a reduction in clinical arrhythmic events. Confirmation in prospective randomized trials is warranted.
No takes yet. Share an insight, caveat, or question.
Traş et al. (2026) conducted an observational in Type 2 diabetes mellitus (n=700). Dapagliflozin vs. Continued pre-existing antidiabetic therapy was evaluated on QT, QTc, QT dispersion, Tp-e, Tp-e/QT, and Tp-e/QTc (Cohen's d 0.48-1.08, p=<0.001). Dapagliflozin initiation was associated with greater reductions in ECG markers of ventricular repolarization compared to controls (Cohen's d 0.48-1.08, p<0.001), with the greatest changes in HFrEF.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: