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


Journal

Circulation. Heart failure
ISSN: 1941-3297
Titre abrégé: Circ Heart Fail
Pays: United States
ID NLM: 101479941

Informations de publication

Date de publication:
05 2023
Historique:
medline: 18 5 2023
pubmed: 1 5 2023
entrez: 1 5 2023
Statut: ppublish

Résumé

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). 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. 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 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. URL: https://www. gov; Unique identifier: NCT02924727.

Sections du résumé

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
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.

Identifiants

pubmed: 37125529
doi: 10.1161/CIRCHEARTFAILURE.122.010259
doi:

Substances chimiques

sacubitril 17ERJ0MKGI
pro-brain natriuretic peptide (1-76) 0
Natriuretic Peptide, Brain 114471-18-0
Ramipril L35JN3I7SJ
Biomarkers 0
Valsartan 80M03YXJ7I
Peptide Fragments 0

Banques de données

ClinicalTrials.gov
['NCT02924727']

Types de publication

Randomized Controlled Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e010259

Commentaires et corrections

Type : CommentIn

Auteurs

Karola S Jering (KS)

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.).

Brian L Claggett (BL)

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.).

Marc A Pfeffer (MA)

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.).

Christopher B Granger (CB)

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

Lars Køber (L)

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

Eldrin F Lewis (EF)

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

Aldo P Maggioni (AP)

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

Douglas L Mann (DL)

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

John J V McMurray (JJV)

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

Margaret F Prescott (MF)

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

Jean L Rouleau (JL)

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

Scott D Solomon (SD)

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.).

Phillippe Gabriel Steg (PG)

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.).

Dirk von Lewinski (D)

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

Eugene Braunwald (E)

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.).

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Classifications MeSH