Diagnosing Myocardial Injury in an Acute Chest Pain Cohort; Long-Term Prognostic Implications of Cardiac Troponin T and I

Author:

Saeed Nasir1ORCID,Steiro Ole-Thomas2ORCID,Langørgen Jørund2,Tjora Hilde L3ORCID,Bjørneklett Rune O34,Skadberg Øyvind5,Bonarjee Vernon V S6,Mjelva Øistein R7,Norekvål Tone M12,Steinsvik Trude8ORCID,Vikenes Kjell12ORCID,Omland Torbjørn910,Aakre Kristin M1211ORCID

Affiliation:

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

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

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

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

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

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

7. Department of Medicine, Stavanger University Hospital , Stavanger , Norway

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

9. Institute of Clinical Medicine, University of Oslo , Oslo , Norway

10. K.G. Jebsen Centre for Cardiac Biomarkers, Institute of Clinical Medicine, University of Oslo , Oslo , Norway

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

Abstract

Abstract Background There are limited data regarding the utility of follow-up cardiac troponin (cTn) measurements after admission for acute chest pain and how long-term stability of myocardial injury and prognostic value differ when using cardiac troponin T (cTnT) or I (cTnI). Methods We measured high-sensitivity (hs)-cTnT (Roche Diagnostics) and hs-cTnI (Siemens Healthineers) during hospitalization for acute chest pain and after 3 months. Acute myocardial injury was defined as concentrations > sex-specific upper reference limit (URL) during hospitalization and ≤URL at 3-months. Chronic myocardial injury (CMI) was defined as concentrations > URL at both time points. Patients were followed from the 3-month sampling point for a median of 1586 (IQR 1161–1786) days for a primary composite endpoint of all-cause mortality, myocardial infarction (MI), revascularization, and heart failure, and a secondary endpoint of all-cause mortality. Results Among 754 patients, 33.8% (hs-cTnT) and 19.2% (hs-cTnI) had myocardial injury during hospitalization. The rate of CMI was 5 times higher by hs-cTnT (20%) assay than hs-cTnI (4%), while acute myocardial injury was equally common; 14% (hs-cTnT) and 15% (hs-cTnI), respectively (6% and 5% when excluding index non-ST-elevation MI (NSTEMI). For hs-cTnT, peak index concentration, 3-month concentration and classification of CMI predicted the primary endpoint; hazard ratios (HRs) 1.38 (95% CI 1.20–1.58), 2.34 (1.70–3.20), and 2.31 (1.30–4.12), respectively. For hs-cTnI, peak index concentration predicted the primary endpoint; HR 1.14 (1.03–1.25). This association was nonsignificant after excluding index NSTEMI. Conclusions Acute myocardial injury is equally frequent, whereas CMI is more prevalent using hs-cTnT assay than hs-cTnI. Measuring hs-cTnT 3 months after an acute chest pain episode could assist in further long-term risk assessment. ClinicalTrials.gov Registration Number: NCT02620202

Publisher

Oxford University Press (OUP)

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