Convalescent troponin and cardiovascular death following acute coronary syndrome.


Journal

Heart (British Cardiac Society)
ISSN: 1468-201X
Titre abrégé: Heart
Pays: England
ID NLM: 9602087

Informations de publication

Date de publication:
11 2019
Historique:
received: 18 03 2019
revised: 17 06 2019
accepted: 21 06 2019
pubmed: 25 7 2019
medline: 17 6 2020
entrez: 25 7 2019
Statut: ppublish

Résumé

High-sensitivity cardiac troponin testing is used in the diagnosis of acute coronary syndromes but its role during convalescence is unknown. We investigated the long-term prognostic significance of serial convalescent high-sensitivity cardiac troponin concentrations following acute coronary syndrome. In a prospective multicentre observational cohort study of 2140 patients with acute coronary syndrome, cardiac troponin I concentrations were measured in 1776 patients at 4 and 12 months following the index event. Patients were stratified into three groups according to the troponin concentration at 4 months using the 99th centile (women>16 ng/L, men>34 ng/L) and median concentration of those within the reference range. The primary outcome was cardiovascular death. Troponin concentrations at 4 months were measurable in 99.0% (1759/1776) of patients (67±12 years, 72% male), and were ≤5 ng/L (median) and >99th centile in 44.8% (795) and 9.3% (166), respectively. There were 202 (11.4%) cardiovascular deaths after a median of 4.8 years. After adjusting for the Global Registry of Acute Coronary Events score, troponin remained an independent predictor of cardiovascular death (HR 1.4, 95% CI 1.3 to 1.5 per doubling) with the highest risk observed in those with increasing concentrations at 12 months. Patients with 4-month troponin concentrations >99th centile were at increased risk of cardiovascular death compared with those ≤5 ng/L (29.5% (49/166) vs 4.3% (34/795); adjusted HR 4.9, 95% CI 3.8 to 23.7). Convalescent cardiac troponin concentrations predict long-term cardiovascular death following acute coronary syndrome. Recognising this risk by monitoring troponin may improve targeting of therapeutic interventions. ACTRN12605000431628;Results.

Identifiants

pubmed: 31337669
pii: heartjnl-2019-315084
doi: 10.1136/heartjnl-2019-315084
pmc: PMC6855795
doi:

Substances chimiques

Biomarkers 0
Troponin I 0

Banques de données

ANZCTR
['ACTRN12605000431628']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1717-1724

Subventions

Organisme : British Heart Foundation
ID : CH/09/002/26360
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/16/14/32023
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/15/51/31596
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: NLM has received consultancy, research grants and speaker fees from manufacturers of cardiac troponin testing including Abbott Diagnostics, Roche and Singulex. AMR has received consultancy, research grants and speaker fees from manufacturers of cardiac troponin testing including Abbott Diagnostics and Roche Diagnostics. AS has received consultancy from Abbott Diagnostics. PDA, DM, AP, JWP, KP, DEN, CE, CP, RWT and RND report no other potential conflict of interest relevant to this article.

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Auteurs

Philip D Adamson (PD)

Christchurch Heart Institute, University of Otago Christchurch, Christchurch, New Zealand.
British Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.

David McAllister (D)

McAllister, David, Edinburgh, UK.

Anna Pilbrow (A)

Christchurch Heart Institute, University of Otago Christchurch, Christchurch, New Zealand.

John William Pickering (JW)

Medicine, University of Otago, Christchurch, New Zealand.

Katrina Poppe (K)

Epidemiology & Biostatistics, University of Auckland, Auckland, New Zealand.

Anoop Shah (A)

BHF/University Centre for Cardiovascular Science, Royal Infirmary of Edinburgh, Edinburgh, UK.

Gillian Whalley (G)

Department of Medicine, University of Otago, Dunedin, New Zealand.

Chris Ellis (C)

Cardiology, Greenlane CVS Services, Auckland City Hospital, Auckland, New Zealand.

Nicholas L Mills (NL)

BHF Centre for Cardiovascular Sciences, The University of Edinburgh, Edinburgh, UK.

David E Newby (DE)

Centre for Cardiovascular Sciences, University of Edinburgh, Edinburgh, UK.

Chris Pemberton (C)

Christchurch Heart Institute, University of Otago Christchurch, Christchurch, New Zealand.

Richard W Troughton (RW)

Cardiology, Christchurch Hospital, Christchurch, New Zealand.
Medicine, University of Otago, Christchurch, New Zealand.

Rob N Doughty (RN)

Department of Medicine, University of Auckland, Auckland, New Zealand.

A Mark Richards (AM)

Christchurch Heart Institute, University of Otago Christchurch, Christchurch, New Zealand.

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Classifications MeSH