Key result
SGLT2 inhibitors linked to ~6-point improvement in RV global longitudinal strain in HFpEF.
Why the study?
Although SGLT2 inhibitors have demonstrated overall cardiovascular benefit, their specific impact on right ventricular performance and RV-arterial uncoupling in patients with HFpEF remained incompletely defined.
Does SGLT2 inhibitor therapy improve right ventricular systolic function, strain parameters, and RV-PA coupling in patients with HFpEF?
Observational (n=100)
No
Does SGLT2 inhibitor therapy improve right ventricular systolic function, strain parameters, and RV-PA coupling in patients with HFpEF?
Six months of SGLT2 inhibitor therapy in patients with HFpEF is associated with significant improvements in right ventricular systolic function, myocardial strain, pulmonary artery pressures, and RV-PA coupling, alongside reductions in NT-proBNP.
SGLT2i-associated RV improvements in HFpEF warrant cautious interpretation; extends prior HF benefits but leaves open causal confirmation in RCTs.
Background Right ventricular (RV) dysfunction and RV–arterial uncoupling contribute substantially to symptoms and prognosis in heart failure with preserved ejection fraction (HFpEF). Although Sodium–glucose cotransporter 2 inhibitors (SGLT2 i) have demonstrated overall cardiovascular benefit, their specific impact on RV performance in HFpEF remains incompletely defined. Purpose To assess the effect of SGLT2 inhibitor therapy on right ventricular systolic function, strain parameters, and RV–PA coupling in patients with HFpEF. Methods In this prospective single-center study, 100 SGLT2 inhibitor–naïve HFpEF patients were initiated on SGLT2i therapy (at a dose 10 mg/day) and followed for six months. Clinical evaluation, NT-proBNP measurement, and detailed echocardiographic assessment including conventional RV systolic parameters, RV strain analysis and RV–PA coupling were performed before and 6-months after regular SGLT2i administration Results Thirty-five percent of patients had reduced RV global longitudinal strain (RV GLS <18%) at baseline. The cohort was predominantly female (82%), the mean age of patients was 64.55 ± 9.27 years and the mean body mass index (BMI) was 37.04 ± 7.21 kg/m2. Comorbidities included hypertension (96%), diabetes mellitus (52%), dyslipidemia (64%), and atrial fibrillation (53%). After six months, the NT-proBNP levels significantly decreased (median 176.5 pg/mL and range 10940 pg/mL vs median 683 pg/mL and range 34772.1 pg/mL at baseline, p-value ≤0.001). Echocardiography revealed a significant reduction in estimated pulmonary artery systolic pressure (25.25 ± 9.26 mmHg vs 36.32 ± 9.50 mmHg at baseline, p-value ≤0.001). Conventional RV systolic parameters improved significantly, including tricuspid annular plane systolic excursion (TAPSE) (26.89 ± 4.41 mm vs 24.64 ± 5.18 mm at baseline, p-value ≤0.001), fractional area change (51.34 ± 6.14 % vs 44.68 ± 6.62 % at baseline, p-value ≤0.001), and tricuspid annulus tissue Doppler S`-wave velocity (13.84 ± 2.30 cm/s vs 12.59 ± 2.36 cm/s at baseline, p-value ≤0.001). Speckle-tracking analysis demonstrated significant improvement in RV GLS (-26.47 ± 5.59 % vs -20.63 ± 5.16 % at baseline, p-value ≤0.001) and RV free wall strain (-31.05 ± 6.21 % vs -26.99 ± 6.53 % at baseline, p-value ≤0.001). RV–PA coupling improved significantly (1.26 ± 0.61 vs 0.73 ± 0.28 at baseline, p-value ≤0.001), reflecting better ventriculo-vascular interaction. Conclusion SGLT2 inhibitor therapy was associated with significant improvement in RV systolic function, myocardial deformation, pulmonary pressures and RV–PA coupling in patients with HFpEF. These findings highlight a potential role of SGLT2 inhibitors in targeting right ventricular dysfunction and improving overall hemodynamic performance in HFpEF.
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Ashraf et al. (2026) conducted an observational in Heart failure with preserved ejection fraction (HFpEF) (n=100). SGLT2 inhibitor vs. Baseline (pre-treatment) was evaluated on Right ventricular systolic function, strain parameters (RV GLS), and RV-PA coupling at 6 months (p=≤0.001). SGLT2 inhibitor therapy for 6 months significantly improved RV global longitudinal strain (-26.47% vs -20.63%, p≤0.001) and RV-PA coupling (1.26 vs 0.73, p≤0.001) in HFpEF patients.
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