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Endothelial Progenitor Cell Number to Apoptotic Endothelial Cell-Derived Micro Particles Ratio in Chronic Heart Failure Phenotypes | OMICS International| Abstract

Atherosclerosis: Open Access
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  • Short Communication   
  • Atheroscler Open Access 2017, Vol 2(1): 108

Endothelial Progenitor Cell Number to Apoptotic Endothelial Cell-Derived Micro Particles Ratio in Chronic Heart Failure Phenotypes

Alexander E. Berezin*
Internal Medicine Department, Senior Consultant of Therapeutic Unit, State Medical University of Zaporozhye, 26, Mayakovsky av., Zaporozhye, Ukraine
*Corresponding Author : Alexander E. Berezin, Internal Medicine Department, Senior Consultant of Therapeutic Unit, State Medical University of Zaporozhye, 26, Mayakovsky Av., Zaporozhye, Ukraine, Tel: +380612894585, Email: [email protected]

Received Date: Mar 20, 2017 / Accepted Date: Mar 25, 2017 / Published Date: Mar 31, 2017

Abstract

Heart failure (HF) remains a leading cause of cardiovascular (CV) mortality and morbidity worldwide. Endothelium is considered a target organ that is involved in the pathogenesis of HF at the earliest stages and corresponds to CV risk factors, CV diseases and different phenotypes of HF. Endothelial progenitor cells (EPCs) with pro-angiogenic phenotypes and apoptotic endothelial cell-derived microparticles (EMPs) may reflect the severity of endothelial dysfunction and predict HF phenotypes. Moreover, apoptotic EMPs and EPCs are involved in the function of endogenous endothelial repair system, which contributes in the pathogenesis of HF across all stages. The short communication is dedicated the predictive role of altered ration between both biomarker of HF in the way to individualize the contemporary predictive score.

Keywords: Chronic heart failure; Biomarkers; Endothelial progenitor cells; Endothelial cell-derived microparticles; Prediction

Citation: Berezin AE (2017) Endothelial Progenitor Cell Number to Apoptotic Endothelial Cell-Derived Micro Particles Ratio in Chronic Heart Failure Phenotypes. Atheroscler open access 2:108.

Copyright: © 2017 Berezin AE. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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