Association Between Angiotensin Receptor–Neprilysin Inhibition, Cardiovascular Biomarkers, and Cardiac Remodeling in Heart Failure With Reduced Ejection Fraction

Author:

Murphy Sean P.1ORCID,Prescott Margaret F.2,Maisel Alan S.3,Butler Javed4,Piña Ileana L.5ORCID,Felker G. Michael6ORCID,Ward Jonathan H.2,Williamson Kristin M.2,Camacho Alexander1ORCID,Kandanelly Ritvik R.1,Solomon Scott D.78ORCID,Januzzi James L.189ORCID

Affiliation:

1. Massachusetts General Hospital, Boston (S.P.M., A.C., R.R.K., J.L.J.).

2. Novartis Pharmaceuticals, East Hanover, NJ (M.F.P., J.H.W., K.M.W.).

3. University of California, San Diego School of Medicine (A.S.M.).

4. University of Mississippi Medical Center, Jackson (J.B.).

5. Detroit Medical Center, Detroit, MI (I.L.P.).

6. Duke University Medical Center and Duke Clinical Research Institute, Durham, NC (G.M.F.).

7. Brigham and Women’s Hospital, Boston, MA (S.D.S.).

8. Harvard Medical School, Boston, MA (S.D.S., J.L.J.).

9. Baim Institute for Clinical Research, Boston, MA (J.L.J.).

Abstract

Background: Sacubitril/valsartan (S/V) treatment is associated with reverse cardiac remodeling and reductions in biomarkers reflecting ventricular wall stress and myocardial injury, such as NT-proBNP (N-terminal pro-B-type natriuretic peptide), hs-cTnT (high-sensitivity cardiac troponin T), and soluble suppressor of tumorigenicity 2 (sST2). How longitudinal changes in these biomarkers analyzed collectively are associated with cardiac remodeling in patients with heart failure with reduced ejection fraction treated with S/V is uncertain. Methods: In a prospective study of S/V in patients with heart failure with reduced ejection fraction, this prespecified exploratory analysis included patients with serially collected biomarkers and echocardiographic measures of cardiac remodeling through 12 months of treatment. A multivariate latent growth curve model assessed associations between simultaneous changes in biomarkers and left ventricular ejection fraction and left atrial volume index. Results: Seven hundred fifteen out of 794 total study participants were included (mean age 65 years, 73% male). Mean baseline left ventricular ejection fraction and left atrial volume index were 29% and 40 mL/m 2 , respectively. Adjusted geometric mean baseline concentrations for biomarkers included NT-proBNP of 649 pg/mL, hs-cTnT of 15.9 ng/L, and sST2 of 24.7 ng/mL. Following initiation of S/V, circulating concentrations of NT-proBNP, hs-cTnT, and sST2 significantly decreased within 30 days and remained significantly different than baseline at all subsequent timepoints. From baseline to month 12, decreases in adjusted biomarker concentrations averaged −27.9% (95% CI, −35.1% to −20.7%; P <0.001) for NT-proBNP; −6.7% (95% CI, −8.8% to −4.7%; P <0.001) for hs-cTnT; and −1.6% (95% CI, −2.9% to −0.4%; P <0.001) for sST2. NT-proBNP concentrations were predictive of later changes in hs-cTnT. The magnitude of reductions in NT-proBNP and hs-cTnT concentrations associated with improvements in left ventricular ejection fraction and left atrial volume index. There was no association between changes in sST2 and changes in other measures. Conclusions: Following initiation of S/V, NT-proBNP, hs-cTnT, and sST2 concentrations decreased significantly. Longitudinal changes in NT-proBNP and hs-cTnT together associated with left atrial and left ventricular reverse remodeling. Registration: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT02887183.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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