Key result
The combination of elevated soluble ST2 and highly sensitive Troponin T was strongly associated with an increased risk of sudden cardiac death (HR 6.4) in patients with stable coronary artery disease.
Why the study?
Do elevated biomarkers (sST2, hs-TnT, hs-CRP, BNP) predict sudden cardiac death in patients with coronary artery disease and preserved left ventricular function?
Cohort (n=1,946)
No
Do elevated biomarkers (sST2, hs-TnT, hs-CRP, BNP) predict sudden cardiac death in patients with coronary artery disease and preserved left ventricular function?
Hazard Ratio: 6.4 (95% CI 2.6–15.5)
p-value: p=<0.001
Elevated sST2 and hs-TnT are strong predictors of sudden cardiac death in patients with CAD and preserved LV function, especially when combined.
May support SCD risk stratification in CAD with preserved LVEF; hypothesis-generating pending prospective validation.
AIMS: Biomarkers have shown promising results in risk assessment of cardiovascular events. Their role in predicting the risk of sudden cardiac death (SCD) is not well established. We tested the performance of several biomarkers in risk assessment for SCD in patients with coronary artery disease (CAD) and preserved left ventricular function. METHODS AND RESULTS: The study population consisted of 1,946 CAD patients (68% male; mean age 66.9±8.6 yrs; type 2 diabetes (T2D) 43%) enrolled in the ARTEMIS study. The study subjects underwent examinations with echocardiography and measurement of several biomarkers. The primary endpoint of the study was SCD. During the mean follow up of 76±20 months 50 patients experienced SCD. Elevated high sensitive CRP (hs-CRP, p = 0.001), soluble ST2 (sST2, p<0.001), B-type natriuretic peptide (BNP, p<0.001), and highly sensitive TroponinT (hs-TnT, p<0.001) predicted the occurrence of SCD in univariate analysis. Using the optimal cutoff points, elevated sST2 (≥27.45ng/mL; hazard ratio [HR] 2.7; 95%CI 1.4-5.1, p = 0.003) and hs-TnT (≥15 ng/mL; HR 2.9; 95% CI 1.5-5.6, p = 0.002) were the strongest predictors of SCD followed by hs-CRP (HR 2.4; 95% CI 1.3-4.4, p = 0.004) and BNP (HR 1.9; 95% CI 1.0-3.7, p = 0.046) in adjusted analysis. Combination of elevated hs-TnT and sST2 resulted in adjusted HR of 6.4 (95% CI 2.6-15.5, p<0.001). CONCLUSION: Elevated sST2 and hs-TnT predict the occurrence of SCD among patients with CAD and preserved left ventricular function. The association between sST2, hs-TnT and SCD may be explained by an ongoing myocardial apoptosis followed by fibrosis leading to vulnerability to malignant arrhythmias.
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Lepojärvi et al. (2018) conducted a cohort in Coronary artery disease with preserved left ventricular function (n=1,946). Elevated soluble ST2 and highly sensitive Troponin T vs. Normal levels of sST2 and hs-TnT was evaluated on Sudden cardiac death (HR 6.4, 95% CI 2.6-15.5, p=<0.001). The combination of elevated soluble ST2 and highly sensitive Troponin T was strongly associated with an increased risk of sudden cardiac death (HR 6.4) in patients with stable coronary artery disease.
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