Endothelial microparticles correlate with high-risk angiographic lesions in acute coronary syndromes

Background: Endothelial Microparticles (EMP) are small fragments of endothelial cell membrane shed during apoptosis or activation. Our group has previously reported elevations of EMP in patients with coronary artery disease (CAD), thrombotic thrombocytopenic purpura (TTP), pre-eclampsia, multiple sc...

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Veröffentlicht in:International journal of cardiology 2004-12, Vol.97 (3), p.439-446
Hauptverfasser: Bernal-Mizrachi, Leon, Jy, Wenche, Fierro, Christian, Macdonough, Rick, Velazques, Hermes A., Purow, Joshua, Jimenez, Joaquin J., Horstman, Lawrence L., Ferreira, Alexandre, de Marchena, Eduardo, Ahn, Yeon S.
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Sprache:eng
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Zusammenfassung:Background: Endothelial Microparticles (EMP) are small fragments of endothelial cell membrane shed during apoptosis or activation. Our group has previously reported elevations of EMP in patients with coronary artery disease (CAD), thrombotic thrombocytopenic purpura (TTP), pre-eclampsia, multiple sclerosis (MS), and severe hypertension (HTN). In the present study, we evaluate the possible relationship between EMP levels and the angiographic severity and characteristics of coronary obstructive lesions. Methods: We studied a total of 43 patients undergoing coronary angiography. Fifteen had presented with acute myocardial infarction (MI), 20 with unstable anginas (UA), 5 with stable angina (SA) and 3 with congestive heart failure. Coronary angiography was reviewed and coronary lesions were classified using the Ambrose classification. Coronary stenoses were classified as high and low risk. High-risk included lesions with eccentric appearance (type II), presence of thrombi, or multiple irregularities. Low-risk lesions were defined as concentric or type I. Lesions were also analyzed by degree of stenosis and history of acute coronary syndrome (ACS). EMP in plasma was assayed by flow cytometry. Results: EMP in eccentric type II or multiple irregular lesions (high-risk) were 2.5-fold higher than in type I or concentric (low-risk) lesions, p20%–45%), and five-fold higher than those without stenosis ( p
ISSN:0167-5273
1874-1754
DOI:10.1016/j.ijcard.2003.10.029