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Digital PCR for Quantifying Circulating MicroRNAs in Acute Myocardial Infarction and Cardiovascular Disease
Published on: July 3, 2018
Predictive value of circulating cardiomyocyte-specific cell-free DNA levels for heart failure risk after acute
Yanling Feng1, Yufeng Zhuo1, Hongji Cheng1
1Department of Cardiology, Panyu District He Xian Memorial Hospital, Guangzhou, China.
Insights
Elevated circulating cardiomyocyte-specific cell-free DNA (CS cfDNA) levels predict heart failure (HF) risk after ST-segment elevation myocardial infarction (STEMI). CS cfDNA offers a promising biomarker for HF prediction post-STEMI.
Area of Science:
- Cardiology
- Biomarker Discovery
Background:
- Heart failure (HF) onset after acute ST-segment elevation myocardial infarction (STEMI) indicates disease progression and poor prognosis.
- Identifying reliable biomarkers for HF risk prediction post-STEMI is crucial for patient management.
Purpose of the Study:
- To evaluate circulating cardiomyocyte-specific cell-free DNA (CS cfDNA) as a predictive biomarker for HF development following STEMI.
- To compare the predictive performance of CS cfDNA against established biomarkers like NT-proBNP and sST2.
Main Methods:
- 146 STEMI patients were enrolled and stratified into two groups based on admission CS cfDNA levels (≤164 copies/ml vs. >164 copies/ml).
- Patients were followed for approximately 355 days to monitor HF onset.
- Receiver Operating Characteristic (ROC) curve analysis and Cox proportional hazards regression were employed.
Main Results:
- The high CS cfDNA group (>164 copies/ml) exhibited a significantly higher prevalence of HF (77.4%) compared to the low CS cfDNA group (18.3%, p < 0.001).
- CS cfDNA demonstrated a strong predictive performance for HF post-STEMI with an Area Under the Curve (AUC) of 0.838, outperforming NT-proBNP (AUC=0.726) and sST2 (AUC=0.635).
- Elevated CS cfDNA levels were independently associated with increased HF risk (HR=2.804, p=0.035) and showed a positive correlation with cardiac injury markers.
Conclusions:
- Circulating cardiomyocyte-specific cell-free DNA (CS cfDNA) is a significant and independent predictor of heart failure following STEMI.
- CS cfDNA represents a promising novel biomarker for early risk stratification and clinical management of STEMI patients.
- Further research into CS cfDNA could enhance prognostic evaluation and therapeutic strategies for post-STEMI care.
Introduction:
The onset of heart failure (HF) often signifies disease progression and unfavorable prognoses in cases of acute ST-segment elevation myocardial infarction (STEMI).
Aim:
To explore the potential value of circulating cardiomyocyte-specific cell-free DNA (CS cfDNA) levels as an indicator for predicting risk of HF after acute STEMI.
Material And Methods:
Overall, 146 STEMI patients were included and classified into two groups according to CS cfDNA levels at admission: Group N1: ≤ 164 copies/ml, Group N2: > 164 copies/ml. A follow-up period of approximately 355 days was completed.
Results:
The prevalence of HF in Group N2 was significantly higher than that in Group N1 (77.4% vs. 18.3%, p < 0.001). ROC curve analysis revealed an AUC of 0.838 (95% CI: 0.688-0.899) for CS cfDNA in predicting onset of HF after STEMI. This AUC value was notably elevated in comparison to that of conventional biomarkers, namely NT-proBNP (AUC = 0.726) and soluble suppression of tumorigenicity-2 (sST2) (AUC = 0.635). Cox proportional hazards regression model analysis further confirmed that level of CS cfDNA at the time of admission was an independent predictor of HF following STEMI, with a hazard ratio (HR) of 2.804 and a 95% CI of 1.086-7.243, achieving statistical significance at p = 0.035.Conclusions: There was a significant positive association between CS cfDNA levels and cardiac injury biomarkers (such as cTnI and sST2). CS cfDNA levels may represent a promising and important biomarker for predicting the occurrence of HF after STEMI, providing novel strategies for clinical management and prognostic evaluation of patients.
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