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Published on: January 28, 2020
Multimarker Approach to Identify Patients with Coronary Artery Disease at High Risk for Subsequent Cardiac Adverse
Georgiana-Aura Giurgea1, Katrin Zlabinger2, Alfred Gugerell2
1Department of Angiology, Internal Medicine II, Medical University of Vienna, 1090 Vienna, Austria.
Insights
This study shows a multimarker approach using seven biomarkers can predict cardiac adverse events in coronary artery disease patients. Canonical discriminant analysis offers personalized risk assessment for better patient management.
Area of Science:
- Cardiology
- Biomarker Discovery
- Predictive Analytics
Background:
- Coronary artery disease (CAD) poses a significant risk for adverse cardiac events (AE).
- Accurate prediction of AE is crucial for timely intervention and personalized treatment strategies.
- Existing risk stratification models may not fully capture the dynamic nature of CAD progression.
Purpose of the Study:
- To evaluate a multimarker approach for predicting subsequent cardiac adverse events in CAD patients.
- To assess the combined discriminatory predictive value of seven specific biomarkers.
- To compare the predictive performance of canonical discriminant analysis with traditional logistic regression.
Main Methods:
- Prospective, non-randomized, single-center cohort study with 161 patients.
- Evaluation of seven biomarkers: S100A12, IL1R4, adrenomedullin, copeptin, NGAL, suPAR, and IMA.
- Primary endpoint assessed using canonical discriminant function analysis for AE prediction over 1-year follow-up.
Main Results:
- Canonical discriminant analysis yielded a significant predictive model (Wilk's lambda = 0.78, p < 0.001).
- The multimarker model achieved 79.4% sensitivity and 74.3% specificity in predicting AE.
- The developed model demonstrated superior predictive performance compared to traditional logistic regression models.
Conclusions:
- Canonical discriminant analysis of a multimarker panel effectively predicts cardiac adverse events in CAD patients.
- This approach allows for defining individual patient risk thresholds, facilitating personalized medicine.
- The findings support the integration of these biomarkers into clinical practice for enhanced risk stratification.
Abstract:
In our prospective non-randomized, single-center cohort study (n = 161), we have evaluated a multimarker approach including S100 calcium binding protein A12 (S100A1), interleukin 1 like-receptor-4 (IL1R4), adrenomedullin, copeptin, neutrophil gelatinase-associated lipocalin (NGAL), soluble urokinase plasminogen activator receptor (suPAR), and ischemia modified albumin (IMA) in prediction of subsequent cardiac adverse events (AE) during 1-year follow-up in patients with coronary artery disease. The primary endpoint was to assess the combined discriminatory predictive value of the selected 7 biomarkers in prediction of AE (myocardial infarction, coronary revascularization, death, stroke, and hospitalization) by canonical discriminant function analysis. The main secondary endpoints were the levels of the 7 biomarkers in the groups with/without AE; comparison of the calculated discriminant score of the biomarkers with traditional logistic regression and C-statistics. The canonical correlation coefficient was 0.642, with a Wilk's lambda value of 0.78 and p < 0.001. By using the calculated discriminant equation with the weighted mean discriminant score (centroid), the sensitivity and specificity of our model were 79.4% and 74.3% in prediction of AE. These values were higher than that of the calculated C-statistics if traditional risk factors with/without biomarkers were used for AE prediction. In conclusion, canonical discriminant analysis of the multimarker approach is able to define the risk threshold at the individual patient level for personalized medicine.
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