Heart failure with preserved ejection fraction, red cell distribution width, and sacubitril/valsartan

Author:

Butt Jawad H.12,McDowell Kirsty1,Kondo Toru1,Desai Akshay S.3,Lefkowitz Martin P.4,Packer Milton5,Petrie Mark C.1,Pfeffer Marc A.3,Rouleau Jean L.6,Vaduganathan Muthiah3,Zile Michael R.7,Jhund Pardeep S.1,Køber Lars2,Solomon Scott3,McMurray John J.V.1

Affiliation:

1. British Heart Foundation Cardiovascular Research Centre University of Glasgow 126 University Place Glasgow G12 8TA UK

2. Department of Cardiology Rigshospitalet Copenhagen University Hospital Copenhagen Denmark

3. Cardiovascular Division Brigham and Women's Hospital Boston MA USA

4. Novartis Pharmaceuticals Corporation East Hanover NJ USA

5. Baylor Heart and Vascular Institute Baylor University Medical Center Dallas TX USA

6. Institut de Cardiologie de Montréal Université de Montréal Montreal QC Canada

7. Medical University of South Carolina and Ralph H. Johnson Veterans Administration Medical Center Charleston SC USA

Abstract

AbstractAimsRed cell distribution width (RDW) is a strong prognostic marker in patients with heart failure (HF) and reduced ejection fraction and other conditions. However, very little is known about its prognostic significance in HF with preserved ejection fraction. We examined the relationship between RDW and outcomes and the effect of sacubitril/valsartan, compared with valsartan, on RDW and clinical outcomes in PARAGON‐HF.Methods and resultsPARAGON‐HF enrolled patients with a left ventricular ejection fraction of ≥45%, structural heart disease, and elevated N‐terminal pro‐B‐type natriuretic peptide (NT‐proBNP). The primary endpoint was a composite of total HF hospitalizations and cardiovascular deaths. Median RDW at randomization was 14.1% (interquartile range 13.5–15.0%). Patients with higher RDW levels were more often men and had more comorbidity, a higher heart rate and NT‐proBNP concentration, more advanced New York Heart Association class, and worse Kansas City Cardiomyopathy Questionnaire scores. There was a graded relationship between quartiles of RDW at randomization and the primary endpoint, with a significantly higher risk associated with increasing RDW, even after adjustment for NT‐proBNP and other prognostic variables {Quartile 1, reference; Quartile 2, rate ratio 1.03 [95% confidence interval (CI) 0.83 to 1.28]; Quartile 3, 1.25 [1.01 to 1.54]; Quartile 4, 1.70 [1.39 to 2.08]}. This association was seen for each of the secondary outcomes, including cardiovascular and all‐cause death. Compared with valsartan, sacubitril/valsartan reduced RDW at 48 weeks [mean change −0.09 (95% CI −0.15 to −0.02)]. The effect of sacubitril/valsartan vs. valsartan was not significantly modified by RDW levels at randomization.ConclusionsRDW, a routinely available and inexpensive biomarker, provides incremental prognostic information when added to established predictors. Compared with valsartan, sacubitril/valsartan led to a small reduction in RDW.

Funder

Novartis

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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