Prognostic Importance of NT-proBNP (N-Terminal Pro-B-Type Natriuretic Peptide) Following High-Risk Myocardial Infarction in the PARADISE-MI Trial

Author:

Jering Karola S.1ORCID,Claggett Brian L.1ORCID,Pfeffer Marc A.1ORCID,Granger Christopher B.2ORCID,Køber Lars3ORCID,Lewis Eldrin F.4,Maggioni Aldo P.5ORCID,Mann Douglas L.6ORCID,McMurray John J.V.7ORCID,Prescott Margaret F.8,Rouleau Jean L.9,Solomon Scott D.1ORCID,Steg Phillippe Gabriel10ORCID,von Lewinski Dirk11ORCID,Braunwald Eugene1ORCID

Affiliation:

1. Cardiovascular Division, Brigham and Women’s Hospital and Harvard Medical School Boston, MA (K.S.J., B.L.C., M.A.P., S.D.S., E.B.).

2. Division of Cardiology, Duke University School of Medicine, Durham, NC (C.B.G.).

3. Heart Centre, Ringshospitalet Copenhagen University Hospital, Denmark (L.K.).

4. Division of Cardiovascular Medicine, Stanford University School of Medicine, Palo Alto, CA (E.F.L.).

5. ANMCO Research Center, Heart Care Foundation, Florence, Italy (A.P.M.).

6. Department of Medicine, Washington University, St Louis, MO (D.L.M.).

7. British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Scotland (J.J.V.M.).

8. Novartis Pharmaceutical Corporation, East Hanover, NJ (M.F.P.).

9. Institut de Cardiologie de Montréal, Université de Montréal, QB, Canada (J.L.R.).

10. Université Paris-Cité, Institut Universitaire de France, AP-HP (Assistance Publique-Hôpitaux de Paris), FACT (French Alliance for Cardiovascular Trials) and INSERM U-1148, Paris, France (P.G.S.).

11. Department of Cardiology, Medical University of Graz, Austria (D.v.L.).

Abstract

Background: NT-proBNP (N-terminal pro-B-type natriuretic peptide) is a potent predictor of death and heart failure (HF) across multiple populations. We evaluated the prognostic importance of NT-proBNP in patients with acute myocardial infarction (MI) complicated by left ventricular systolic dysfunction, pulmonary congestion, or both and ≥1 of 8 risk-augmenting factors enrolled in the PARADISE-MI trial (Prospective ARNI vs ACE Inhibitor Trial to Determine Superiority in Reducing Heart Failure Events After Myocardial Infarction). Methods: Patients were randomized to sacubitril/valsartan 200 mg or ramipril 5 mg twice daily within 0.5 to 7 days of a MI. Patients with prior HF were excluded. NT-proBNP and hs-cTnT (high-sensitivity troponin T) were collected at randomization in a prespecified substudy of 1129 patients. The primary end point of PARADISE-MI was a composite of cardiovascular death or incident HF (hospitalization or outpatient symptomatic HF), analyzed as time-to-first event; additional end points included all-cause death and the composite of fatal or nonfatal MI or stroke. Results: Median NT-proBNP was 1757 ng/L (25th–75th percentiles, 896–3462 ng/L) at randomization (4.0±1.8 days after the index MI). Patients in the highest quartile of NT-proBNP were older, more commonly women and had more hypertension, atrial fibrillation, renal dysfunction, and pulmonary congestion on presentation (all P <0.001). NT-proBNP was strongly associated with the primary end point (adjusted hazard ratio, 1.45 per doubling of NT-proBNP; [95% CI, 1.23–1.70]), adjusted for clinical variables and baseline hs-cTnT. NT-proBNP was also independently associated with all-cause death (adjusted hazard ratio, 1.74 [95% CI, 1.38–2.21]) and fatal or nonfatal MI or stroke (adjusted hazard ratio, 1.24 [95% CI, 1.05–1.45]). NT-proBNP did not significantly modify the neutral treatment effect of sacubitril/valsartan relative to ramipril ( P interaction=0.46). Conclusions: Within the first week of a high-risk MI NT-proBNP is associated with incident HF, death and atherosclerotic events. This prognostic information is independent of hs-cTnT. Registration: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT02924727.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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