High-Sensitivity Cardiac Troponin T and Recurrent Vascular Events After First Ischemic Stroke
Jan F Scheitz1,2,3, Jess Lim2, Leonie H A Broersen1,2
1Center for Stroke Research Berlin (CSB) Charité Universitätsmedizin Berlin Berlin Germany.
Insights
Elevated high-sensitivity cardiac troponin T (hs-cTnT) levels predict a higher risk of recurrent vascular events and death after a first ischemic stroke. This association shows a dose-response relationship, highlighting hs-cTnT
Area of Science:
- Cardiology
- Neurology
- Biomarkers
Background:
- Cardiac troponin levels are increasingly recognized as indicators of vascular risk.
- High-sensitivity cardiac troponin T (hs-cTnT) is a sensitive biomarker for myocardial injury.
- Previous research suggests a link between troponin levels and vascular complications.
Purpose of the Study:
- To investigate the association between hs-cTnT levels and the risk of recurrent vascular events and death in patients experiencing their first mild to moderate ischemic stroke.
- To determine if hs-cTnT levels can aid in stratifying risk for post-stroke complications.
Main Methods:
- Utilized data from the Prospective Cohort With Incident Stroke Berlin (PROSCIS-B) study.
- Employed Cox proportional hazards regression to analyze the relationship between baseline hs-cTnT levels and a composite outcome of recurrent stroke, myocardial infarction, and all-cause death.
- Analyzed data from 562 patients with a mean follow-up of 3 years.
Main Results:
- Patients with hs-cTnT levels above the upper reference limit (14 ng/L) had a significantly higher incidence of the primary outcome (27.3% vs. 10.2%).
- An adjusted hazard ratio of 2.0 (95% CI, 1.3-3.3) indicated increased risk for those with elevated hs-cTnT.
- A clear dose-response relationship was observed, with the highest hs-cTnT quartile showing a 4.8-fold increased risk (adjusted HR, 4.8; 95% CI, 1.9-11.8) compared to the lowest.
Conclusions:
- Baseline hs-cTnT levels are dose-dependently associated with an increased risk of recurrent vascular events and all-cause death within 3 years following a first ischemic stroke.
- Elevated hs-cTnT may serve as a valuable biomarker for identifying patients at higher risk of adverse vascular outcomes after stroke.
- Further research is warranted to explore the clinical utility of hs-cTnT for individualized risk stratification in stroke patients.
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.
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