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Digital PCR for Quantifying Circulating MicroRNAs in Acute Myocardial Infarction and Cardiovascular Disease
Published on: July 3, 2018
Cell-Free circulating DNA: a new biomarker for the acute coronary syndrome
Ming Cui1, Mengkang Fan, Rongrong Jing
1Center of Laboratory Medicine, Affiliated Hospital of Nantong University, Nantong, China.
Insights
Elevated cell-free circulating DNA (cf-DNA) levels are significantly higher in acute coronary syndrome (ACS) patients. This finding suggests cf-DNA may serve as a diagnostic and prognostic biomarker for ACS severity and risk stratification.
Area of Science:
- Biochemistry
- Cardiology
- Molecular Diagnostics
Background:
- Cell-free circulating DNA (cf-DNA) concentrations correlate with prognosis in various diseases.
- The association between cf-DNA and acute coronary syndrome (ACS) is not well-established.
- Detection of cf-DNA in ACS using branched DNA (bDNA)-based Alu assay lacks data.
Purpose of the Study:
- To investigate cf-DNA concentrations in ACS patients.
- To explore the relationship between cf-DNA levels and clinical features in ACS.
- To evaluate cf-DNA as a potential biomarker in ACS.
Main Methods:
- Plasma cf-DNA concentrations were measured using a bDNA-based Alu assay.
- 137 ACS patients, 60 healthy individuals, and 13 stable angina (SA) patients were included.
- Correlations with Gensini and GRACE scores were analyzed.
Main Results:
- ACS patients exhibited significantly higher plasma cf-DNA concentrations compared to healthy and SA controls.
- ST-segment elevation myocardial infarction patients showed the highest cf-DNA levels.
- Positive correlations were observed between cf-DNA and Gensini/GRACE scoring in ACS.
Conclusions:
- cf-DNA may serve as a valuable marker for ACS diagnosis.
- cf-DNA can potentially predict coronary artery lesion severity.
- Elevated cf-DNA levels aid in risk stratification for ACS patients.
Background:
In recent studies, concentrations of cell-free circulating DNA (cf-DNA) have been correlated with clinical characteristics and prognosis in several diseases. The relationship between cf-DNA concentrations and the acute coronary syndrome (ACS) remains unknown. Moreover, no data are available for the detection cf-DNA in ACS by a branched DNA (bDNA)-based Alu assay. The aim of the present study was to investigate cf-DNA concentrations in ACS and their relationship with clinical features.
Methods:
Plasma cf-DNA concentrations of 137 ACS patients at diagnosis, of 60 healthy individuals and of 13 patients with stable angina (SA) were determined using a bDNA-based Alu assay.
Results:
ACS patients (median 2,285.0, interquartile range 916.4-4,857.3 ng/ml), especially in ST-segment elevation myocardial infarction patients (median 5,745.4, interquartile range 4,013.5-8,643.9 ng/ml), showed a significant increase in plasma cf-DNA concentrations compared with controls (healthy controls: median 118.3, interquartile range 81.1-221.1 ng/ml; SA patients: median 202.3, interquartile range 112.7-256.1 ng/ml) using a bDNA-based Alu assay. Moreover, we found positive correlations between cf-DNA and Gensini scoring and GRACE (Global Registry of Acute Coronary Events) scoring in ACS.
Conclusion:
cf-DNA may be a valuable marker for diagnosing and predicting the severity of coronary artery lesions and risk stratification in ACS.
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