High‐Sensitivity Cardiac Troponin T and Recurrent Vascular Events After First Ischemic Stroke

Author:

Scheitz Jan F.123ORCID,Lim Jess2,Broersen Leonie H. A.12ORCID,Ganeshan Ramanan12,Huo Shufan12ORCID,Sperber Pia S.14ORCID,Piper Sophie K.56ORCID,Heuschmann Peter U.78ORCID,Audebert Heinrich J.12,Nolte Christian H.12435ORCID,Siegerink Bob1ORCID,Endres Matthias12439ORCID,Liman Thomas G.12

Affiliation:

1. Center for Stroke Research Berlin (CSB) Charité Universitätsmedizin Berlin Berlin Germany

2. Klinik für Neurologie mit Experimenteller Neurologie Charité–Universitätsmedizin Berlin Berlin Germany

3. German Center for Neurodegenerative Diseases (Deutsches Zentrum für Neurodegenerative Erkrankungen), partner site Berlin Germany

4. German Center for Cardiovascular Research (Deutsches Zentrum für Herz‐Kreislaufforschung, DHZK), partner site Berlin Germany

5. Berlin Institute of Health (BIH) Germany

6. Institute of Biometry and Clinical Epidemiology Charité–Universitätsmedizin Berlin Berlin Germany

7. Institute of Clinical Epidemiology and Biometry University of Würzburg Germany

8. Clinical Trial Center University Hospital Würzburg Germany

9. ExcellenceCluster NeuroCure Berlin Germany

Abstract

Background Recent evidence suggests cardiac troponin levels to be a marker of increased vascular risk. We aimed to assess whether levels of high‐sensitivity cardiac troponin T (hs‐cTnT) are associated with recurrent vascular events and death in patients with first‐ever, mild to moderate ischemic stroke. Methods and Results We used data from the PROSCIS‐B (Prospective Cohort With Incident Stroke Berlin) study. We computed Cox proportional hazards regression analyses to assess the association between hs‐cTnT levels upon study entry (Roche Elecsys, upper reference limit, 14 ng/L) and the primary outcome (composite of recurrent stroke, myocardial infarction, and all‐cause death). A total of 562 patients were analyzed (mean age, 67 years [SD 13]; 38.6% women; median National Institutes of Health Stroke Scale=2; hs‐cTnT above upper reference limit, 39.2%). During a mean follow‐up of 3 years, the primary outcome occurred in 89 patients (15.8%), including 40 (7.1%) recurrent strokes, 4 (0.7%) myocardial infarctions, and 51 (9.1%) events of all‐cause death. The primary outcome occurred more often in patients with hs‐cTnT above the upper reference limit (27.3% versus 10.2%; adjusted hazard ratio, 2.0; 95% CI, 1.3–3.3), with a dose‐response relationship when the highest and lowest hs‐cTnT quartiles were compared (15.2 versus 1.8 events per 100 person‐years; adjusted hazard ratio, 4.8; 95% CI, 1.9–11.8). This association remained consistent in sensitivity analyses, which included age matching and stratification for sex. Conclusions Hs‐cTnT is dose‐dependently associated with an increased risk of recurrent vascular events and death within 3 years after first‐ever, mild to moderate ischemic stroke. These findings support further studies of the utility of hs‐cTnT for individualized risk stratification after stroke. Registration URL: https://www.clinicaltrials.gov ; Unique identifier: NCT01363856.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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