Novel biomarker-driven prognostic models to predict morbidity and mortality in chronic heart failure: the EMPEROR-Reduced trial.


Journal

European heart journal
ISSN: 1522-9645
Titre abrégé: Eur Heart J
Pays: England
ID NLM: 8006263

Informations de publication

Date de publication:
14 11 2021
Historique:
received: 31 05 2021
revised: 09 07 2021
accepted: 11 08 2021
pubmed: 24 8 2021
medline: 25 11 2021
entrez: 23 8 2021
Statut: ppublish

Résumé

The aim of this study was to generate a biomarker-driven prognostic tool for patients with chronic HFrEF. Circulating levels of N-terminal pro B-type natriuretic peptide (NT-proBNP) and high-sensitivity cardiac troponin T (hs-cTnT) each have a marked positive relationship with adverse outcomes in heart failure with reduced ejection fraction (HFrEF). A risk model incorporating biomarkers and clinical variables has not been validated in contemporary heart failure (HF) trials. In EMPEROR-Reduced, 33 candidate variables were pre-selected. Multivariable Cox regression models were developed using stepwise selection for: (i) the primary composite outcome of HF hospitalization or cardiovascular death, (ii) all-cause death, and (iii) cardiovascular mortality. A total of 3730 patients were followed up for a median of 16 months, 823 (22%) patients had a primary outcome and 515 (14%) patients died, of whom 389 (10%) died from a cardiovascular cause. NT-proBNP and hs-cTnT were the dominant predictors of the primary outcome, and in addition, a shorter time since last HF hospitalization, longer time since HF diagnosis, lower systolic blood pressure, New York Heart Association (NYHA) Class III or IV, higher heart rate and peripheral oedema were key predictors (eight variables in total, all P < 0.001). The primary outcome risk score discriminated well (c-statistic = 0.73), with patients in the top 10th of risk having an event rate >9 times higher than those in the bottom 10th. Empagliflozin benefitted patients across risk levels for the primary outcome. NT-proBNP and hs-cTnT were also the dominant predictors of all-cause and cardiovascular mortality, followed by NYHA Class III or IV and ischaemic aetiology (four variables in total, all P < 0.001). The mortality risk model presented good event discrimination for all-cause and cardiovascular mortality (c-statistic = 0.69 for both). These simple models were externally validated in the BIOSTAT-CHF study, achieving similar c-statistics. The combination of NT-proBNP and hs-cTnT with a small number of readily available clinical variables provides prognostic assessment for patients with HFrEF. This predictive tool kit can be easily implemented for routine clinical use.

Identifiants

pubmed: 34423361
pii: 6356321
doi: 10.1093/eurheartj/ehab579
pmc: PMC8599073
doi:

Substances chimiques

Biomarkers 0
Peptide Fragments 0
Troponin T 0
Natriuretic Peptide, Brain 114471-18-0

Banques de données

ClinicalTrials.gov
['NCT03057977']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

4455-4464

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the European Society of Cardiology.

Références

J Am Coll Cardiol. 2019 Sep 3;74(9):1205-1217
pubmed: 31466618
Circulation. 2021 Jan 26;143(4):326-336
pubmed: 33081531
Circ Heart Fail. 2014 Jul;7(4):590-5
pubmed: 24874200
Eur J Heart Fail. 2020 Jan;22(1):81-89
pubmed: 31793144
Am Heart J. 2006 Jan;151(1):76-83
pubmed: 16368295
Circ Heart Fail. 2020 Jun;13(6):e006946
pubmed: 32482089
JAMA Cardiol. 2020 Apr 1;5(4):432-441
pubmed: 31995119
Eur J Heart Fail. 2018 Feb;20(2):323-331
pubmed: 29314455
JACC Heart Fail. 2021 Jan;9(1):42-51
pubmed: 33189630
Eur Heart J. 2013 May;34(19):1404-13
pubmed: 23095984
Circ Heart Fail. 2017 Jun;10(6):
pubmed: 28615366
J Am Coll Cardiol. 2010 Sep 28;56(14):1071-8
pubmed: 20863950
N Engl J Med. 2020 Oct 8;383(15):1413-1424
pubmed: 32865377
Lancet Glob Health. 2017 Jul;5(7):e665-e672
pubmed: 28476564
Circulation. 2018 Oct 16;138(16):1666-1676
pubmed: 29871978
JACC Heart Fail. 2019 Feb;7(2):158-168
pubmed: 30611722
Eur J Heart Fail. 2017 May;19(5):627-634
pubmed: 28247565
Lancet. 2020 Sep 19;396(10254):819-829
pubmed: 32877652
Eur J Prev Cardiol. 2020 Dec;27(2_suppl):12-18
pubmed: 33238734
JAMA. 2019 Sep 17;322(11):1085-1095
pubmed: 31475295
Eur J Heart Fail. 2019 Jan;21(1):40-49
pubmed: 30537261
Eur J Heart Fail. 2019 Oct;21(10):1270-1278
pubmed: 31584231
Circ Heart Fail. 2021 Jun;14(6):e008410
pubmed: 33998243
Circulation. 2006 Mar 21;113(11):1424-33
pubmed: 16534009
Eur J Heart Fail. 2018 Feb;20(2):373-381
pubmed: 29027329
Eur J Heart Fail. 2016 Jun;18(6):716-26
pubmed: 27126231
JACC Heart Fail. 2018 Jun;6(6):452-462
pubmed: 29852929

Auteurs

Stuart J Pocock (SJ)

Department of Medical Statistics, London School of Hygiene and Tropical Medicine, London, UK.

João Pedro Ferreira (JP)

Université de Lorraine, Inserm, Centre d'Investigations Cliniques Plurithématique 1433, and Inserm U1116, CHRU, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France.
Cardiovascular Research and Development Center, Department of Surgery and Physiology, Faculty of Medicine of the University of Porto, Porto, Portugal.

John Gregson (J)

Department of Medical Statistics, London School of Hygiene and Tropical Medicine, London, UK.

Stefan D Anker (SD)

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

Javed Butler (J)

Department of Medicine, University of Mississippi, Jackson.

Gerasimos Filippatos (G)

Department of Cardiology, Attikon University Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Nicholas D Gollop (ND)

Boehringer Ingelheim International GmbH, Ingelheim, Germany.

Tomoko Iwata (T)

Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach, Germany.

Martina Brueckmann (M)

Boehringer Ingelheim International GmbH, Ingelheim, Germany.
Faculty of Medicine Mannheim, University of Heidelberg, Mannheim, Germany.

James L Januzzi (JL)

Massachusetts General Hospital, Boston, MA, USA.
Harvard Medical School, Boston, MA, USA.
Baim Institute for Clinical Research, Boston, MA, USA.

Adriaan A Voors (AA)

University of Groningen, Groningen, The Netherlands.

Faiez Zannad (F)

Université de Lorraine, Inserm, Centre d'Investigations Cliniques Plurithématique 1433, and Inserm U1116, CHRU, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France.

Milton Packer (M)

Baylor Heart and Vascular Institute, Baylor University Medical Center, Dallas, TX, USA.
Imperial College London, London, UK.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH