Impaired Right Ventricular-Pulmonary Arterial Coupling and Effect of Sildenafil in Heart Failure With Preserved Ejection Fraction: An Ancillary Analysis From the Phosphodiesterase-5 Inhibition to Improve Clinical Status And Exercise Capacity in Diastolic Heart Failure (RELAX) Trial

被引:70
作者
Hussain, Imad [1 ]
Mohammed, Selma F. [1 ]
Forfia, Paul R. [2 ]
Lewis, Gregory D. [3 ]
Borlaug, Barry A. [1 ]
Gallup, Dianne S. [4 ]
Redfield, Margaret M. [1 ]
机构
[1] Mayo Clin, Div Cardiovasc Dis, 200 First St SW, Rochester, MN 55905 USA
[2] Temple Univ, Philadelphia, PA 19122 USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Cardiol, Boston, MA 02115 USA
[4] Duke Clin Res Inst, Durham, NC USA
关键词
diastole; exercise; heart failure; hypertension; pulmonary hypertension; RANDOMIZED CONTROLLED-TRIAL; PLANE SYSTOLIC EXCURSION; VENTILATORY EFFICIENCY; CARDIAC STRUCTURE; OXYGEN-UPTAKE; HYPERTENSION; HEMODYNAMICS; 1-YEAR; DYSFUNCTION; PROGNOSIS;
D O I
10.1161/CIRCHEARTFAILURE.115.002729
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Right ventricular (RV) dysfunction (RVD) is a poor prognostic factor in heart failure with preserved ejection fraction (HFpEF). The physiological perturbations associated with RVD or RV function indexed to load (RV-pulmonary arterial [PA] coupling) in HFpEF have not been defined. HFpEF patients with marked impairment in RV-PA coupling may be uniquely sensitive to sildenafil. Methods and Results In a subset of HFpEF patients enrolled in the Phosphodiesteas-5 Inhibition to Improve Clinical Status And Exercise Capacity in Diastolic Heart Failure (RELAX) trial, physiological variables and therapeutic effect of sildenafil were examined relative to the severity of RVD (tricuspid annular plane systolic excursion [TAPSE]) and according to impairment in RV-PA coupling (TAPSE/pulmonary artery systolic pressure) ratio. The prevalence of atrial fibrillation and diuretic use, n-terminal probrain natriuretic peptide levels, renal dysfunction, neurohumoral activation, myocardial necrosis and fibrosis biomarkers, and the severity of diastolic dysfunction all increased with severity of RVD. Peak oxygen consumption decreased and ventilatory inefficiency (VE/VCO2 slope) increased with increasing severity of RVD. Many but not all physiological derangements were more closely associated with the TAPSE/pulmonary artery systolic pressure ratio. Compared with placebo, at 24 weeks, TAPSE decreased, and peak oxygen consumption and VE/CO2 slope were unchanged with sildenafil. There was no interaction between RV-PA coupling and treatment effect, and sildenafil did not improve TAPSE, peak oxygen consumption, or VE/VCO2 in patients with pulmonary hypertension and RVD. Conclusions HFpEF patients with RVD and impaired RV-PA coupling have more advanced heart failure. In RELAX patients with RVD and impaired RV-PA coupling, sildenafil did not improve RV function, exercise capacity, or ventilatory efficiency.
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