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Published on: January 15, 2022
Risk classification of highly sensitive troponin I predict presence of vulnerable plaque assessed by dual source
Ting Liu1, Guan Wang1, Peiling Li1
1Department of Radiology, The First Affiliated Hospital of China Medical University, 155 Nanjing Bei St, Heping District, Shenyang, China.
Insights
Highly sensitive troponin I (hsTn I) combined with coronary computed tomography angiography (DSCTA) can improve acute coronary syndrome (ACS) risk classification. Early DSCTA assessment of stenosis and plaque features aids in identifying high-risk patients with intermediate hsTn I levels.
Area of Science:
- Cardiology
- Medical Imaging
- Biomarkers
Background:
- Patients with acute chest pain and negative initial troponin/ECG require serial testing for acute coronary syndrome (ACS).
- Highly sensitive troponin I (hsTn I) is a key biomarker, but its association with coronary plaque characteristics needs further elucidation.
- Coronary dual-source computed tomography angiography (DSCTA) can visualize plaque morphology and stenosis.
Purpose of the Study:
- To investigate the association between hsTn I levels and vulnerable plaque features on DSCTA.
- To determine if combining hsTn I with early DSCTA improves risk stratification for ACS.
- To enhance the diagnostic accuracy for ACS in patients with intermediate hsTn I levels.
Main Methods:
- A study included 220 patients with acute chest pain, negative ECG, and conventional troponin, who underwent DSCTA and hsTn I measurement.
- Patients were categorized into low, intermediate, and high hsTn I risk groups.
- DSCTA was assessed for significant stenosis, plaque types, and vulnerable plaque features.
Main Results:
- ACS occurred in 16.3% of patients; prevalence of significant stenosis and high-risk plaque increased with hsTn I levels.
- No ACS events were observed in the low hsTn I group.
- ACS incidence was 10.1% in the intermediate hsTn I group and 52.3% in the high hsTn I group.
- Combined hsTn I and DSCTA improved ACS diagnostic accuracy, particularly in the intermediate risk group.
Conclusions:
- Increasing hsTn I levels correlate with coronary stenosis severity and vulnerable plaque presence detected by DSCTA.
- Early DSCTA assessment of stenosis and high-risk plaque features, alongside hsTn I, refines ACS risk stratification.
- This combined approach enhances diagnostic accuracy for ACS, especially in intermediate-risk patients.
Abstract:
Patients presenting to the emergency department with acute chest pain, negative conventional troponin and electrocardiogram require serial testing to rule out acute coronary syndrome (ACS). We studied the association of highly sensitive troponin (hsTn) I with vulnerable plaque features as detected by coronary dual source computed tomography angiography (DSCTA) and determined whether hsTn I at the time of presentation combined with early DSCTA could improve classification of patients as high-risk or low risk for ACS. We included 220 patients with acute chest pain, negative electrocardiogram and conventional troponin who underwent DSCTA and had hsTn I measured at the time of presentation. The patients were categorized as having hsTn I below the limit of detection (low risk), intermediate and above the 99th percentile (high risk). Readers assessed DSCTA qualitatively for the presence of significant CAD (≥50% stenosis), calcified and non-calcified coronary plaque, and vulnerable plaque features (positive remodeling, low CT attenuation plaque, napkin-ring sign, spotty calcium). The mean age of the population was 50.3 ± 8.2 years (43% women). ACS during the index hospitalization occurred in 36 (16.3%) patients (myocardial infarction n = 8, unstable angina pectoris n = 28). HsTn I was below the limit of detection, intermediate, and above 99th percentile in 39 (17.7%), 139 (86.9%), and 42 (19.1%) patients, respectively. Across the categories of low risk, intermediate and high risk of hsTn I, there was increase in prevalence of ≥50% stenosis (0, 11.5, and 61.9% of patients; p < 0.001), any plaque (35.9, 51.1, and 85.7% of patients; p < 0.001) and high-risk plaque (0, 36.0, and 85.7% of patients; p < 0.001). None of the patients in low risk HsTn I group had ACS. ACS occurred in 10.1% of the intermediate hsTn I group and in 52.3% of the patients with high risk hsTnI group. Severity of stenosis and presence of vunerable plaque as detected by DSCTA are associated with increasing levels of hsTn I. DSCTA at the time of presentation with the assessment for both stenosis and high-risk plaque improved the diagnostic accuracy for ACS in the intermediate hsTn I group patients.
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