Prognostic significance of chronic myocardial injury diagnosed by three different cardiac troponin assays in patients admitted with suspected acute coronary syndrome

Author:

Steiro Ole-Thomas1,Langørgen Jørund1,Tjora Hilde L.2,Bjørneklett Rune O.23,Skadberg Øyvind4,Bonarjee Vernon V.S.5,Mjelva Øistein R.6,Steinsvik Trude7,Lindahl Bertil89,Omland Torbjørn1011,Aakre Kristin M.11213ORCID,Vikenes Kjell112

Affiliation:

1. Department of Heart Disease , Haukeland University Hospital , Bergen , Norway

2. Emergency Care Clinic , Haukeland University Hospital , Bergen , Norway

3. Department of Clinical Medicine , University of Bergen , Bergen , Norway

4. Laboratory of Medical Biochemistry , Stavanger University Hospital , Stavanger , Norway

5. Department of Cardiology , Stavanger University Hospital , Stavanger , Norway

6. Department of Internal Medicine , Stavanger University Hospital , Stavanger , Norway

7. Department of Laboratory Medicine , Vestre Viken Hospital Trust , Bærum , Norway

8. Department of Medical Sciences , Uppsala University Hospital , Uppsala , Sweden

9. Uppsala Clinical Research Center , Uppsala , Sweden

10. Center for Heart Failure Research , Institute of Clinical Medicine, University of Oslo , Oslo , Norway

11. Department of Cardiology , Akershus University Hospital , Oslo , Norway

12. Department of Clinical Science , University of Bergen , Bergen , Norway

13. Department of Medical Biochemistry and Pharmacology , Haukeland University Hospital , Bergen , Norway

Abstract

Abstract Objectives Chronic myocardial injury (CMI) is defined as stable concentrations of cardiac troponin T or I (cTnT or cTnI) above the assay-specific 99th percentile upper reference limit (URL) and signals poor outcome. The clinical implications of diagnosing CMI are unclear. We aimed to assess prevalence and association of CMI with long-term prognosis using three different high-sensitivity cTn (hs-cTn) assays. Methods A total of 1,292 hospitalized patients without acute myocardial injury had cTn concentrations quantified by hs-cTn assays by Roche Diagnostics, Abbott Diagnostics and Siemens Healthineers. The median follow-up time was 4.1 years. The prevalence of CMI and hazard ratios for mortality and cardiovascular (CV) events were calculated based on the URL provided by the manufacturers and compared to the prognostic accuracy when lower percentiles of cTn (97.5, 95 or 90), limit of detection or the estimated bioequivalent concentrations between assays were used as cutoff values. Results There was no major difference in prognostic accuracy between cTnT and cTnI analyzed as continuous variables. The correlation between cTnT and cTnI was high (r=0.724–0.785), but the cTnT assay diagnosed 3.9–4.5 times more patients with having CMI based on the sex-specific URLs (TnT, n=207; TnI Abbott, n=46, TnI Siemens, n=53) and had higher clinical sensitivity and AUC at the URL. Conclusions The prevalence of CMI is highly assay-dependent. cTnT and cTnI have similar prognostic accuracy for mortality or CV events when measured as continuous variables. However, a CMI diagnosis according to cTnT has higher prognostic accuracy compared to a CMI diagnosis according to cTnI.

Funder

Helse Vest

Grieg Foundation

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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