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Updated: Apr 25, 2026

Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
Small-size circulating endothelial microparticles in coronary artery disease
Shuai-Shuai Hu1, Hong-Gang Zhang1, Qiu-Ju Zhang1
1Institute of Microcirculation, Peking Union Medical College & Chinese Academy of Medical Sciences; Key Laboratory of Microcirculation, National Health and Family Planning Commission, Beijing, China.
Small endothelial microparticles (SEMPs) show promise as a biomarker for monitoring endothelial dysfunction in coronary artery disease (CAD). Elevated CD62E(+) SEMPs indicate potential endothelial dysfunction in CAD patients.
Area of Science:
- Cardiovascular Research
- Biomarker Discovery
- Endothelial Biology
Background:
- Endothelial microparticles (EMPs) are emerging biomarkers for endothelial dysfunction in coronary artery disease (CAD).
- Limited data exist on the detection and significance of small microparticles (diameter <0.5 µm).
Purpose of the Study:
- To investigate the detection of small-size endothelial microparticles (SEMPs) in CAD patients.
- To assess the utility of SEMPs as biomarkers for monitoring endothelial dysfunction in CAD.
Main Methods:
- Flow cytometry was used to quantify CD31(+)/CD42b- SEMPs and CD62E(+) SEMPs.
- The study included 19 CAD patients and 14 healthy controls.
- Clinical parameters were recorded for correlation analysis.
Main Results:
- The percentage of CD62E(+) SEMPs was significantly higher in CAD patients compared to healthy subjects.
- The receiver operating characteristic curve analysis indicated a cut-off value of 1.35 for CD62E(+) SEMPs (AUC = 0.795).
- No significant correlation was found between CD62E(+) SEMP levels and clinical parameters.
Conclusions:
- The percentage of CD62E(+) SEMPs is a potential biomarker for assessing endothelial function in CAD.
- SEMPs, particularly CD62E(+) SEMPs, may aid in monitoring endothelial dysfunction in coronary artery disease.
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