医学
达帕格列嗪
内科学
心脏病学
心力衰竭
射血分数
复极
糖尿病
血糖性
QT间期
心室复极
心电图
促心律失常
心源性猝死
心房颤动
观察研究
Copeptin蛋白
长QT综合征
多非利特
作者
Gülüzar Traş,Fuat Polat,Melike Saday Bozkurt,İsmail Altıntaş
标识
DOI:10.1080/03007995.2026.2741494
摘要
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.
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