Effect of Empagliflozin on Hemodynamics in Patients With Heart Failure and Reduced Ejection Fraction
[摘要] BACKGROUND Inhibition of the sodium-glucose cotransporter-2 (SGLT2i) improves outcomes in patients with heart failure (HF) and reduced ejection fraction (HFrEF), but the mechanism by which they improve outcomes remains unclear. OBJECTIVES This study aimed to investigate the effects of sodium-glucose cotransporter-2 inhibitor empagliflozin on central hemodynamics in patients with HF and HFrEF. METHODS This investigator-initiated, double-blinded, placebo-controlled, randomized trial enrolled 70 patients with HFrEF from March 6, 2018, to September 10, 2019. Patients were assigned to empagliflozin of 10 mg or matching placebo once daily on guideline-driven HF therapy for 12 weeks. The primary outcome was ratio of pulmonary capillary wedge pressure (PCWP) to cardiac index (CI) at peak exercise after 12 weeks. Patients underwent right-heart catheterization at rest and during exercise at baseline and 12-week follow-up. RESULTS Patients with HFrEF, mean age of 57 years, mean left-ventricular ejection fraction, 26%, and 12 (17%) with type 2 diabetes mellitus were randomized. There was no significant treatment effect on peak PCWP/CI (-0.13 mm Hg/l/min/m(2); 95% confidence interval: -1.60 to 1.34 mm Hg/l/min/m(2); p = 0.86). Considering hemodynamics over the full range of exercise loads, PCWP was significantly reduced (-2.40 mm Hg; 95% confidence interval: -3.96 to -0.84 mm Hg; p = 0.003), but not CI (-0.09 l/min/m(2); 95% confidence interval: -0.14 to 0.32 l/min/m(2); p = 0.448) by empagliflozin. This was consistent among patients with and without type 2 diabetes. CONCLUSIONS Among patients with stable HFrEF, empagliflozin for 12 weeks reduced PCWP compared with placebo. There was no significant improvement in neither CI nor PCWP/CI at rest or exercise. (C) 2020 by the American College of Cardiology Foundation.
[发布日期] 2020-12-08 [发布机构]
[效力级别] [学科分类]
[关键词] exercise;heart failure reduced ejection fraction;hemodynamics;SGLT2 inhibitor [时效性]