Abstract 4142910: Role of High-Sensitivity Troponin I and Troponin T in Prediction of Sudden Arrhythmic Death in Patients with Coronary Artery Disease

Introduction: While implantable cardiac defibrillators (ICDs) can prevent sudden arrhythmic death (SAD), less than 30% of SAD patients meet criteria for implantation. Improved risk stratification and prediction is necessary to identify individuals at risk. Objective: The purpose of this study was to evaluate the role of high-sensitivity troponin T (hs-TnT) and high sensitivity troponin I (hs-TnI) in predicting SAD. Methods: We prospectively evaluated the associations of hs-TnT and hs-TnI with the incidence of SAD in 5,764 participants enrolled in the PREDETERMINE study, which enrolled individuals with history of coronary artery disease (CAD) not meeting criteria for ICD implantation with left ventricular ejection fraction (LVEF) above 30%. Using multivariable Cox proportional hazards models, hs-TnT and hs-TnI were evaluated as continuous (log-transformed) variables, by quintile, and dichotomously by clinical thresholds. Spearman coefficients were calculated to assess biomarker correlations. Results: Over a median 8.1 years follow-up, 4.3% (n=249) of the study cohort experienced SAD. Within our cohort, hs-TnT and hs-TnI were highly correlated with a Spearman coefficient of 0.77. After multivariable adjustment, both hs-TnT and hs-TnI were associated with increased risk of SAD (HR 1.18, 95% CI 1.03-1.36 per 1-SD change for hs-TnT, and HR 1.19, 95% CI 1.04-1.37 per 1-SD change for hs-TnI). Risk for SAD was elevated in the highest quintile of hs-TnT (HR 2.53, 95% CI 1.47-4.37) and the highest quintile of hs-TnI (HR 3.23, 95% CI 1.86-5.60) compared to the lowest quintile. Elevated hs-TnT ≥19 ng/L (median) was associated with increased risk of SAD (1.69, 95% CI 1.27-2.25), as was hs-TnI ≥ 8.5 ng/L (HR 1.69, 95% CI 1.29-2.23). Conclusion: In our large, prospectively enrolled cohort of participants with CAD and LVEF above 30%, both increased hs-TnT and hs-TnI were each significantly associated with similarly increased risks of SAD. Among individuals who are at risk for SAD but do not qualify for prevention with ICD implantation, measurement of high-sensitivity troponin in conjunction with clinical data may help to identify those most likely to benefit from preventative therapy.

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Journal
Circulation
Published
2024-11-12
DOI
https://doi.org/10.1161/circ.150.suppl_1.4142910
Primary Topic
Acute Myocardial Infarction Research
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article
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article

Abstract 4142910: Role of High-Sensitivity Troponin I and Troponin T in Prediction of Sudden Arrhythmic Death in Patients with Coronary Artery Disease

Jessica Mao, Chi‐Hong Tseng, Natasha Cuk, M. Vinayaga Moorthy et al.
Circulation
Acute Myocardial Infarction Research
article

Abstract 4142910: Role of High-Sensitivity Troponin I and Troponin T in Prediction of Sudden Arrhythmic Death in Patients with Coronary Artery Disease

Jessica Mao, Chi‐Hong Tseng, Natasha Cuk, M. Vinayaga Moorthy, Christine M. Albert, D. John Morrow, Alan H. Kadish, Nancy R. Cook, Yunxian Liu
article en

Abstract

Introduction: While implantable cardiac defibrillators (ICDs) can prevent sudden arrhythmic death (SAD), less than 30% of SAD patients meet criteria for implantation. Improved risk stratification and prediction is necessary to identify individuals at risk. Objective: The purpose of this study was to evaluate the role of high-sensitivity troponin T (hs-TnT) and high sensitivity troponin I (hs-TnI) in predicting SAD. Methods: We prospectively evaluated the associations of hs-TnT and hs-TnI with the incidence of SAD in 5,764 participants enrolled in the PREDETERMINE study, which enrolled individuals with history of coronary artery disease (CAD) not meeting criteria for ICD implantation with left ventricular ejection fraction (LVEF) above 30%. Using multivariable Cox proportional hazards models, hs-TnT and hs-TnI were evaluated as continuous (log-transformed) variables, by quintile, and dichotomously by clinical thresholds. Spearman coefficients were calculated to assess biomarker correlations. Results: Over a median 8.1 years follow-up, 4.3% (n=249) of the study cohort experienced SAD. Within our cohort, hs-TnT and hs-TnI were highly correlated with a Spearman coefficient of 0.77. After multivariable adjustment, both hs-TnT and hs-TnI were associated with increased risk of SAD (HR 1.18, 95% CI 1.03-1.36 per 1-SD change for hs-TnT, and HR 1.19, 95% CI 1.04-1.37 per 1-SD change for hs-TnI). Risk for SAD was elevated in the highest quintile of hs-TnT (HR 2.53, 95% CI 1.47-4.37) and the highest quintile of hs-TnI (HR 3.23, 95% CI 1.86-5.60) compared to the lowest quintile. Elevated hs-TnT ≥19 ng/L (median) was associated with increased risk of SAD (1.69, 95% CI 1.27-2.25), as was hs-TnI ≥ 8.5 ng/L (HR 1.69, 95% CI 1.29-2.23). Conclusion: In our large, prospectively enrolled cohort of participants with CAD and LVEF above 30%, both increased hs-TnT and hs-TnI were each significantly associated with similarly increased risks of SAD. Among individuals who are at risk for SAD but do not qualify for prevention with ICD implantation, measurement of high-sensitivity troponin in conjunction with clinical data may help to identify those most likely to benefit from preventative therapy.

CirculationVol. 150(Suppl_1)
Cedars-Sinai Medical Center (US), Brigham and Women's Hospital (US), University of California, Los Angeles (US), Touro College (US), University Health System (US)
Good health and well-being
Openalex Percentile: Top 62%
Acute Myocardial Infarction Research
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