Cardiovascular and non-cardiovascular death distinction: the utility of troponin beyond N-terminal pro-B-type natriuretic peptide. Findings from the BIOSTAT-CHF study.

Cardiovascular death Events Heart failure Natriuretic peptides Non-cardiovascular death Risk Troponin

Journal

European journal of heart failure
ISSN: 1879-0844
Titre abrégé: Eur J Heart Fail
Pays: England
ID NLM: 100887595

Informations de publication

Date de publication:
01 2020
Historique:
received: 13 06 2019
revised: 24 09 2019
accepted: 27 09 2019
pubmed: 4 12 2019
medline: 18 5 2021
entrez: 4 12 2019
Statut: ppublish

Résumé

Heart failure (HF) patients are at high-risk of cardiovascular (CV) events, including CV death. Nonetheless, a substantial proportion of these patients die from non-CV causes. Identifying patients at higher risk for each individual event may help selecting patients for clinical trials and tailoring cardiovascular therapies. The aims of the present study are to: (i) characterize patients according to CV vs. non-CV death; (ii) develop models for the prediction of the respective events; (iii) assess the models' performance to differentiate CV from non-CV death. This study included 2309 patients with HF from the BIOSTAT-CHF (a systems BIOlogy Study to TAilored Treatment in Chronic Heart Failure) study. Competing-risk models were used to assess the best combination of variables associated with each cause-specific death. Results were validated in an independent cohort of 1738 HF patients. The best model to predict CV death included low blood pressure, estimated glomerular filtration rate ≤ 60 mL/min, peripheral oedema, previous HF hospitalization, ischaemic HF, chronic obstructive pulmonary disease, elevated N-terminal pro-B-type natriuretic peptide (NT-proBNP), and troponin (c-index = 0.73). The non-CV death model incorporated age > 75 years, anaemia and elevated NT-proBNP (c-index = 0.71). Both CV and non-CV death rose by quintiles of the risk scores; yet these models allowed the identification of patients in whom absolute CV death rates clearly outweigh non-CV death ones. These findings were externally replicated, but performed worse in a less severely diseased population. Risk models for predicting CV and non-CV death allowed the identification of patients at higher absolute risk of dying from CV causes (vs. non-CV ones). Troponin helped in predicting CV death only, whereas NT-proBNP helped in the prediction of both CV and non-CV death. These findings can be useful both for tailoring therapies and for patient selection in HF trials in order to attain CV event enrichment.

Identifiants

pubmed: 31793144
doi: 10.1002/ejhf.1654
doi:

Substances chimiques

Biomarkers 0
Peptide Fragments 0
Troponin 0
pro-brain natriuretic peptide (1-76) 0
Natriuretic Peptide, Brain 114471-18-0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

81-89

Subventions

Organisme : European Commission
ID : FP7-242209-BIOSTAT-CHF
Pays : International
Organisme : European Commission
ID : EudraCT 2010-020808-29
Pays : International
Organisme : French National Research Agency Fighting Heart Failure
ID : ANR-15-RHU-0004
Pays : International
Organisme : French PIA project 'Lorraine Université d'Excellence' GEENAGE
ID : ANR-15-IDEX-04-LUE
Pays : International

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2019 The Authors. European Journal of Heart Failure © 2019 European Society of Cardiology.

Références

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Auteurs

João Pedro Ferreira (JP)

Université de Lorraine, Inserm, Centre d'Investigations Cliniques- Plurithématique 14-33, and Inserm U1116, CHRU, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France.

Wouter Ouwerkerk (W)

National Heart Centre Singapore, Hospital Drive, Singapore.
Department of Dermatology, Amsterdam UMC, Amsterdam Infection & Immunity Institute, University of Amsterdam, Amsterdam, The Netherlands.

Jasper Tromp (J)

National Heart Centre Singapore, Hospital Drive, Singapore.
Department of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.

Leong Ng (L)

Department of Cardiovascular Sciences, NIHR Leicester Biomedical Research Centre, Glenfield Hospital, University of Leicester, Leicester, UK.

Kenneth Dickstein (K)

Stavanger University Hospital, University of Bergen, Bergen, Norway.

Stefan Anker (S)

Department of Cardiology (CVK), and Berlin-Brandenburg Center for Regenerative Therapies (BCRT), German Centre for Cardiovascular Research (DZHK) partner site Berlin, Charité Universitätsmedizin, Berlin, Germany.

Gerasimos Filippatos (G)

National and Kapodistrian University of Athens, Attikon General Hospital, Athens, Greece.
University of Cyprus, School of Medicine, Nicosia, Cyprus.

John G Cleland (JG)

Robertson Centre for Biostatistics and Clinical Trials, University of Glasgow, Glasgow, UK.
National Heart and Lung Institute, Imperial College London, London, UK.

Marco Metra (M)

Institute of Cardiology, Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.

Dirk J van Veldhuisen (DJ)

Department of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.

Adriaan A Voors (AA)

Department of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.

Faiez Zannad (F)

Université de Lorraine, Inserm, Centre d'Investigations Cliniques- Plurithématique 14-33, and Inserm U1116, CHRU, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France.

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