Isosorbide Dinitrate, With or Without Hydralazine, Does Not Reduce Wave Reflections, Left Ventricular Hypertrophy, or Myocardial Fibrosis in Patients With Heart Failure With Preserved Ejection Fraction

Author:

Zamani Payman1,Akers Scott2,Soto‐Calderon Haideliza1,Beraun Melissa1,Koppula Maheswara R.1,Varakantam Swapna1,Rawat Deepa1,Shiva‐Kumar Prithvi1,Haines Philip G.13,Chittams Jesse4,Townsend Raymond R.5,Witschey Walter R.6,Segers Patrick7,Chirinos Julio A.1

Affiliation:

1. Division of Cardiovascular Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA

2. Department of Radiology, Philadelphia Veterans' Affairs Medical Center, Philadelphia, PA

3. Rhode Island Hospital, Warren Alpert Medical School of Brown University, Providence, RI

4. Office of Nursing Research, School of Nursing, University of Pennsylvania, Philadelphia, PA

5. Division of Nephrology/Hypertension, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA

6. Department of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA

7. Biofluid, Tissue, and Solid Mechanics for Medical Applications, IBiTech, iMinds Medical IT, Ghent University, Ghent, Belgium

Abstract

Background Wave reflections, which are increased in patients with heart failure with preserved ejection fraction, impair diastolic function and promote pathologic myocardial remodeling. Organic nitrates reduce wave reflections acutely, but whether this is sustained chronically or affected by hydralazine coadministration is unknown. Methods and Results We randomized 44 patients with heart failure with preserved ejection fraction in a double‐blinded fashion to isosorbide dinitrate ( ISDN ; n=13), ISDN +hydralazine ( ISDN +hydral; n=15), or placebo (n=16) for 6 months. The primary end point was the change in reflection magnitude ( RM ; assessed with arterial tonometry and Doppler echocardiography). Secondary end points included change in left ventricular mass and fibrosis, measured with cardiac magnetic resonance imaging, and the 6‐minute walk distance. ISDN reduced aortic characteristic impedance (mean baseline=0.15 [95% CI , 0.14–0.17], 3 months=0.11 [95% CI , 0.10–0.13], 6 months=0.10 [95% CI , 0.08–0.12] mm Hg/mL per second; P =0.003) and forward wave amplitude (P f , mean baseline=54.8 [95% CI , 47.6–62.0], 3 months=42.2 [95% CI , 33.2–51.3]; 6 months=37.0 [95% CI , 27.2–46.8] mm Hg, P =0.04), but had no effect on RM ( P =0.64), left ventricular mass ( P =0.33), or fibrosis ( P =0.63). ISDN +hydral increased RM (mean baseline=0.39 [95% CI , 0.35–0.43]; 3 months=0.31 [95% CI , 0.25–0.36]; 6 months=0.44 [95% CI , 0.37–0.51], P =0.03), reduced 6‐minute walk distance (mean baseline=343.3 [95% CI , 319.2–367.4]; 6 months=277.0 [95% CI , 242.7–311.4] meters, P =0.022), and increased native myocardial T1 (mean baseline=1016.2 [95% CI , 1002.7–1029.7]; 6 months=1054.5 [95% CI , 1036.5–1072.3], P =0.021). A high proportion of patients experienced adverse events with active therapy ( ISDN =61.5%, ISDN +hydral=60.0%; placebo=12.5%; P =0.007). Conclusions ISDN , with or without hydralazine, does not exert beneficial effects on RM , left ventricular remodeling, or submaximal exercise and is poorly tolerated. ISDN +hydral appears to have deleterious effects on RM , myocardial remodeling, and submaximal exercise. Our findings do not support the routine use of these vasodilators in patients with heart failure with preserved ejection fraction. Clinical Trial Registration URL : www.clinicaltrials.gov . Unique identifier: NCT 01516346.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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