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Clinical Trial
. 2016 Apr;9(4):e002729.
doi: 10.1161/CIRCHEARTFAILURE.115.002729.

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

Affiliations
Clinical Trial

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

Imad Hussain et al. Circ Heart Fail. 2016 Apr.

Abstract

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.

Clinical trial registration: URL: http://www.clinicaltrials.gov. Unique identifier: NCT00763867.

Keywords: diastole; exercise; heart failure; hypertension; pulmonary hypertension.

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Figures

Figure 1
Figure 1. Changes in RV function, exercise capacity and ventilatory efficiency in Sildenafil vs placebo treated patients according to right ventricular – pulmonary artery coupling
Bars show the least square means with 95% confidence intervals from a model which include baseline values (excluded for change in TAPSE model), randomized treatment, RV-PA coupling subgroups and the interaction between randomized treatment and RV-PA coupling subgroup. Abbreviations: Nl, normal; RV, right ventricular; RVD, RV dysfunction; PH, pulmonary hypertension; TAPSE, tricuspid annular plane systolic excursion; pVO2, peak oxygen consumption; VE/VCO2, expiratory to carbon dioxide volume ratio

References

    1. Iglesias-Garriz I, Olalla-Gomez C, Garrote C, Lopez-Benito M, Martin J, Alonso D, Rodriguez MA. Contribution of right ventricular dysfunction to heart failure mortality: A meta-analysis. Rev Cardiovasc Med. 2012;13:e62–e69. - PubMed
    1. Mohammed SF, Hussain I, AbouEzzeddine OF, Takahama H, Kwon SH, Forfia P, Roger VL, Redfield MM. Right ventricular function in heart failure with preserved ejection fraction: A community based study. Circulation. 2014;130:2310–2320. - PMC - PubMed
    1. Melenovsky V, Hwang SJ, Lin G, Redfield MM, Borlaug BA. Right heart dysfunction in heart failure with preserved ejection fraction. Eur Heart J. 2014;35:3452–3462. - PMC - PubMed
    1. Shah SJ, Katz DH, Selvaraj S, Burke MA, Yancy CW, Gheorghiade M, Bonow RO, Huang CC, Deo RC. Phenomapping for novel classification of heart failure with preserved ejection fraction. Circulation. 2014;131:269–279. - PMC - PubMed
    1. Bursi F, McNallan SM, Redfield MM, Nkomo VT, Lam CS, Weston SA, Jiang R, Roger VL. Pulmonary pressures and death in heart failure: A community study. J Am Coll Cardiol. 2012;59:222–231. - PMC - PubMed

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