Diagnostic and prognostic performance of the ratio between high-sensitivity cardiac troponin I and troponin T in patients with chest pain.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2022
Historique:
received: 04 05 2022
accepted: 11 10 2022
entrez: 1 11 2022
pubmed: 2 11 2022
medline: 4 11 2022
Statut: epublish

Résumé

Elevations of high-sensitivity cardiac troponin (hs-cTn) concentrations not related to type 1 myocardial infarction are common in chest pain patients presenting to emergency departments. The discrimination of these patients from those with type 1 myocardial infarction (MI) is challenging and resource-consuming. We aimed to investigate whether the hs-cTn I/T ratio might provide diagnostic and prognostic increment in this context. We calculated the hs-cTn I/T ratio in 888 chest pain patients having hs-cTnI (Abbott Laboratories) or hs-cTnT (Roche Diagnostics) concentrations above the respective 99th percentile at 2 hours from presentation. All patients were followed for one year regarding mortality. The median hs-cTn I/T ratio was 3.45 (25th, 75th percentiles 1.80-6.59) in type 1 MI patients (n = 408 ☯46.0%]), 1.18 (0.81-1.90) in type 2 MI patients (n = 56 ☯6.3%]) and 0.67 (0.39-1.12) in patients without MI. The hs-cTn I/T ratio provided good discrimination of type 1 MI from no type 1 MI (area under the receiver-operator characteristic curve 0.89 ☯95% confidence interval 0.86-0.91]), of type 1 MI from type 2 MI (area under the curve 0.81 ☯95% confidence interval 0.74-0.87]), and was associated with type 1 MI in adjusted analyses. The hs-cTn I/T ratio provided no consistent prognostic value. The hs-cTn I/T ratio appears to be useful for early diagnosis of type 1 MI and its discrimination from type 2 MI in chest pain patients presenting with elevated hs-cTn. Differences in hs-cTn I/T ratio values may reflect variations in hs-cTn release mechanisms in response to different types of myocardial injury.

Sections du résumé

BACKGROUND
Elevations of high-sensitivity cardiac troponin (hs-cTn) concentrations not related to type 1 myocardial infarction are common in chest pain patients presenting to emergency departments. The discrimination of these patients from those with type 1 myocardial infarction (MI) is challenging and resource-consuming. We aimed to investigate whether the hs-cTn I/T ratio might provide diagnostic and prognostic increment in this context.
METHODS
We calculated the hs-cTn I/T ratio in 888 chest pain patients having hs-cTnI (Abbott Laboratories) or hs-cTnT (Roche Diagnostics) concentrations above the respective 99th percentile at 2 hours from presentation. All patients were followed for one year regarding mortality.
RESULTS
The median hs-cTn I/T ratio was 3.45 (25th, 75th percentiles 1.80-6.59) in type 1 MI patients (n = 408 ☯46.0%]), 1.18 (0.81-1.90) in type 2 MI patients (n = 56 ☯6.3%]) and 0.67 (0.39-1.12) in patients without MI. The hs-cTn I/T ratio provided good discrimination of type 1 MI from no type 1 MI (area under the receiver-operator characteristic curve 0.89 ☯95% confidence interval 0.86-0.91]), of type 1 MI from type 2 MI (area under the curve 0.81 ☯95% confidence interval 0.74-0.87]), and was associated with type 1 MI in adjusted analyses. The hs-cTn I/T ratio provided no consistent prognostic value.
CONCLUSIONS
The hs-cTn I/T ratio appears to be useful for early diagnosis of type 1 MI and its discrimination from type 2 MI in chest pain patients presenting with elevated hs-cTn. Differences in hs-cTn I/T ratio values may reflect variations in hs-cTn release mechanisms in response to different types of myocardial injury.

Identifiants

pubmed: 36318533
doi: 10.1371/journal.pone.0276645
pii: PONE-D-22-13082
pmc: PMC9624427
doi:

Substances chimiques

Biomarkers 0
Troponin I 0
Troponin T 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0276645

Déclaration de conflit d'intérêts

Dr Eggers has consulted for Roche Diagnostics. Professor Cullen has consulted for Abbott Diagnostics, Siemens Healthineers and Beckman Coulter. Dr Parsonage has consulted for Abbott Diagnostics and Siemens Healthineers. Professor Cullens and Dr Parsonages institution has received research funding from Abbott Diagnostics, Siemens Healthineers and Beckman Coulter. Professor Pickering has consulted for Abbott Diagnostics. Professor Richards has consulted for and/or received grants/in-kind support from Roche Diagnostics, Abbott Laboratories and Thermo Fisher. Dr Than has consulted for Abbott Diagnostics, Radiometer, Roche Diagnostics, Siemens Healthineers and received funding from Abbott Diagnostics, Beckman Coulter and Roche Diagnostics. The authors have declared that no competing interests exist.

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Auteurs

Kai M Eggers (KM)

Department of Medical Sciences and Uppsala Clinical Research Center, Uppsala University, Uppsala, Sweden.

Ola Hammarsten (O)

Department of Clinical Chemistry, Sahlgrenska University Hopsital, Göteborg, Sweden.

Sally J Aldous (SJ)

Department of Cardiology, Christchurch Hospital, Christchurch, New Zealand.

Louise Cullen (L)

Emergency Department, Royal Brisbane and Women's Hospital, Brisbane, Australia.

Jaimi H Greenslade (JH)

Emergency Department, Royal Brisbane and Women's Hospital, Brisbane, Australia.

Bertil Lindahl (B)

Department of Medical Sciences and Uppsala Clinical Research Center, Uppsala University, Uppsala, Sweden.

William A Parsonage (WA)

Department of Cardiology, Royal Brisbane and Women's Hospital, Brisbane, Australia.

Christopher J Pemberton (CJ)

Christchurch Heart Institute, Department of Medicine, University of Ontago, Christchurch, New Zealand.

John W Pickering (JW)

Christchurch Heart Institute, Department of Medicine, University of Ontago, Christchurch, New Zealand.
Emergency Department, Christchurch Hospital, Christchurch, New Zealand.

A Mark Richards (AM)

Christchurch Heart Institute, Department of Medicine, University of Ontago, Christchurch, New Zealand.
Cardiovascular Research Institute, National University of Singapore, Singapore, Singapore.

Richard W Troughton (RW)

Christchurch Heart Institute, Department of Medicine, University of Ontago, Christchurch, New Zealand.

Martin P Than (MP)

Emergency Department, Christchurch Hospital, Christchurch, New Zealand.

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Classifications MeSH