Risk Estimates of Imminent Cardiovascular Death and Heart Failure Hospitalization Are Improved Using Serial Natriuretic Peptide Measurements in Patients With Coronary Artery Disease and Type 2 Diabetes.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
19 04 2022
Historique:
pubmed: 7 4 2022
medline: 22 4 2022
entrez: 6 4 2022
Statut: ppublish

Résumé

Background Baseline and temporal changes in natriuretic peptide (NP) concentrations have strong prognostic value with regard to long-term cardiovascular risk stratification. To increase the clinical utility of NP sampling for patient management, we wanted to assess the incremental predictive value of 2 serial NP measurements compared with a single measurement and provide absolute risk estimates for cardiovascular death or heart failure hospitalization (HFH) within 6 months based on 2 serial NP measurements. Methods and Results Consecutive NP samples obtained from 5393 patients with a recent coronary event and type 2 diabetes enrolled in the ELIXA (Evaluation of Cardiovascular Outcomes in Patients With Type 2 Diabetes After Acute Coronary Syndrome During Treatment With Lixisenatide) trial were used to construct best logistic regression models with outcome of cardiovascular death or HFH (136 events). Absolute risk estimates of cardiovascular death or HFH within 6 months using either BNP (B-type natriuretic peptide) or NT-proBNP (N-terminal pro-BNP) serial measurements were depicted based on the concentrations of 2 serial NP measurements. During the 6-month follow-up periods, the incidence rate (±95% CIs) of cardiovascular death or HFH for patients was 14.0 (11.8‒16.6) per 1000 patient-years. Risk prediction depended on NP concentrations from both prior and current sampling. NP sampling 6 months apart improved the predictive value and reclassification of patients compared with a single sample (AUROC [Area Under the Receiver Operating Characteristic curve]: BNP,

Identifiants

pubmed: 35383463
doi: 10.1161/JAHA.121.021327
pmc: PMC9238457
doi:

Substances chimiques

Biomarkers 0
Natriuretic Peptides 0
Peptide Fragments 0
Vasodilator Agents 0
Natriuretic Peptide, Brain 114471-18-0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e021327

Commentaires et corrections

Type : CommentIn

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Auteurs

Emil Wolsk (E)

Division of Cardiovascular Medicine Brigham and Women's Hospital Harvard Medical School Boston MA.
Department of Cardiology Herlev-Gentofte Hospital Herlev Denmark.

Brian Claggett (B)

Division of Cardiovascular Medicine Brigham and Women's Hospital Harvard Medical School Boston MA.

Rafael Diaz (R)

Estudios Clínicos Latinoamérica Rosario Argentina.

Kenneth Dickstein (K)

University of Bergen Stavanger University Hospital Stavanger Norway.

Hertzel C Gerstein (HC)

Division of Endocrinology & Metabolism McMaster University Hamilton ON Canada.

Lars Køber (L)

Department of Cardiology Rigshospitalet Copenhagen Denmark.

Eldrin F Lewis (EF)

Cardiovascular Medicine Department of Medicine Stanford University Stanford CA.

Aldo P Maggioni (AP)

Research Center of the Italian Association of Hospital Cardiologists Florence Italy.
Maria Cecilia Hospital GVM Care & Research Cotignola RA Italy.

John J V McMurray (JJV)

British Heart Foundation Cardiovascular Research Centre University of Glasgow Glasgow United Kingdom.

Jeffrey L Probstfield (JL)

Division of Cardiology University of Washington Medical Center Seattle WA.

Matthew C Riddle (MC)

Division of Endocrinology Oregon Health and Science University Portland OR.

Scott D Solomon (SD)

Division of Cardiovascular Medicine Brigham and Women's Hospital Harvard Medical School Boston MA.

Jean-Claude Tardif (JC)

Montreal Heart Institute Université de Montréal Montreal Canada.

Marc A Pfeffer (MA)

Division of Cardiovascular Medicine Brigham and Women's Hospital Harvard Medical School Boston MA.

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Classifications MeSH