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Updated: Jun 13, 2025

Digital PCR for Quantifying Circulating MicroRNAs in Acute Myocardial Infarction and Cardiovascular Disease
Published on: July 3, 2018
Postmortem-Derived Exosomal MicroRNA 486-5p as Potential Biomarkers for Ischemic Heart Disease Diagnosis
So-Yeon Kim1, Sookyoung Lee2, Jong-Tae Park1
1Department of Forensic Medicine, Chonnam National University Medical School, Gwangju 61469, Republic of Korea.
Abstract:
Exosomes are nanovesicles 30-150 nm in diameter released extracellularly. Those isolated from human body fluids reflect the characteristics of their cells or tissues of origin. Exosomes carry extensive biological information from their parent cells and have significant potential as biomarkers for disease diagnosis and prognosis. However, there are limited studies utilizing exosomes in postmortem diagnostics. In this study, we extended our initial research which identified the presence and established detection methodologies for exosomes in postmortem fluids. We analyzed exosomal miRNA extracted from plasma and pericardial fluid samples of a control group (n = 13) and subjects with acute myocardial infarction (AMI; n = 24). We employed next-generation sequencing (NGS) to investigate whether this miRNA could serve as biomarkers for coronary atherosclerosis leading to acute myocardial infarction. Our analysis revealed 29 miRNAs that were differentially expressed in the AMI group compared to the control group. Among these, five miRNAs exhibited more than a twofold increase in expression across all samples from the AMI group. Specifically, miR-486-5p levels were significantly elevated in patients with high-grade (type VI or above) atherosclerotic plaques, as per the American Heart Association criteria, highlighting its potential as a predictive biomarker for coronary atherosclerosis progression. Our results indicate that postmortem-derived exosomal microRNAs can serve as potential biomarkers for various human diseases, including cardiovascular disorders. This finding has profound implications for forensic diagnostics, a field critically lacking diagnostic markers.
Insights
Postmortem exosomes contain microRNAs (miRNAs) that can diagnose acute myocardial infarction (AMI). Elevated miR-486-5p in exosomes may predict coronary atherosclerosis progression, aiding forensic diagnostics.
Area of Science:
- Biochemistry
- Molecular Biology
- Forensic Science
Background:
- Exosomes, nanovesicles from body fluids, carry biological information and show potential as disease biomarkers.
- Limited research exists on using exosomes for postmortem diagnostics.
- This study investigates exosomal microRNAs (miRNAs) in postmortem samples for diagnosing acute myocardial infarction (AMI) and coronary atherosclerosis.
Purpose of the Study:
- To identify exosomal miRNAs in postmortem plasma and pericardial fluid as potential biomarkers for AMI.
- To assess the utility of these miRNAs in diagnosing coronary atherosclerosis progression.
- To explore the application of postmortem exosomal miRNAs in forensic diagnostics.
Main Methods:
- Analysis of exosomal miRNA from postmortem plasma and pericardial fluid samples using next-generation sequencing (NGS).
- Comparison of miRNA expression profiles between a control group (n=13) and an acute myocardial infarction group (n=24).
- Correlation of specific miRNA levels with the severity of atherosclerotic plaques based on American Heart Association criteria.
Main Results:
- Twenty-nine differentially expressed miRNAs were identified between the AMI and control groups.
- Five miRNAs showed more than a twofold increase in expression in the AMI group.
- miR-486-5p levels significantly correlated with high-grade atherosclerotic plaques, indicating its potential as a predictive biomarker.
Conclusions:
- Postmortem-derived exosomal miRNAs are viable biomarkers for diagnosing cardiovascular diseases like AMI.
- miR-486-5p shows promise as a predictive biomarker for coronary atherosclerosis progression.
- These findings have significant implications for advancing forensic diagnostics with novel molecular markers.
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