Abstract

Aims: We aimed to assess the prognostic role of copeptin in patients presenting to the emergency department with acute symptoms and increased high-sensitivity cardiac troponin T. Methods: A total of 3890 patients presenting with acute symptoms to the emergency department of Heidelberg University Hospital were assessed for increased hs-cTnT (>14 ng/L) from three cohorts: the Heidelberg Acute Coronary Syndrome (ACS) Registry (n = 2477), the BIOPS Registry (n = 320), and the ACS OMICS Registry (n = 1093). In a pooled analysis, 1956 patients remained, comprising of 1600 patients with ACS and 356 patients with non-ACS. Results: Median follow-up was 1468 days in the ACS cohort and 709 days in the non-ACS cohort. Elevated copeptin levels (>10 pmol/L) were found in 1174 patients (60.0%) in the entire cohort (58.1% in ACS and 68.5% in non-ACS, respectively) and mortality rates were significantly higher than in patients with normal copeptin levels (29.0% vs. 10.7%, p < 0.001). In a multivariate Cox regression, elevated copeptin was independently associated with all-cause death in the ACS (HR = 1.7, 1.3–2.3, p = 0.002) and non-ACS cohort (HR = 2.7, 1.4–5.0, p = 0.0018). Conclusion: Copeptin may aid in identifying patients at risk for adverse outcomes in patients with increased levels of hs-cTnT in ACS patients and in non-ACS conditions.

Highlights

  • Copeptin is a marker of endogenous stress and the most promising application in clinical practice is the combination with cardiac troponin for early rule-out of acute myocardial infarction (AMI) in patients presenting with symptoms suggestive of acute coronary syndrome (ACS) [1,2,3]

  • The aim of the ConTrACS study was to assess the prognostic impact of copeptin in patients with increased hs-cTnT presenting to the emergency department with acute symptoms, including ACS and non-ACS conditions

  • Elevated copeptin levels (>10 pmol/L) on admission were found in 1174 patients (60.0%) in the entire cohort as well as 58.1% in ACS and 68.5% in non-ACS, respectively

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Summary

Introduction

Copeptin is a marker of endogenous stress and the most promising application in clinical practice is the combination with cardiac troponin (cTn) for early rule-out of acute myocardial infarction (AMI) in patients presenting with symptoms suggestive of acute coronary syndrome (ACS) [1,2,3]. A dual-marker strategy (DMS) with normal levels of copeptin and conventional cTn is recommended by guidelines for non-ST-elevation myocardial infarction [4,5]. Elevated copeptin values in patients with suspected ACS and non-ACS conditions were found to confer incremental prognostic information beyond an increased hs-cTn [10,14]. The aim of the ConTrACS study was to assess the prognostic impact of copeptin in patients with increased hs-cTnT presenting to the emergency department with acute symptoms, including ACS and non-ACS conditions

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