Abstract

Background and PurposeWe evaluated the hypothesis that the number of circulating EPC could be associated with the risk of stroke recurrence (SR) or vascular events (VE) after an ischemic stroke.MethodsWe studied prospectively consecutive patients with cerebral infarction within the first 48 hours after the onset. We recorded demographic factors, vascular risk factors, previous Rankin scale (RS) score, and etiology. We analyzed EPC counts by flow cytometry in blood collected at day 7 and defined EPC as CD34+/CD133+/KDR+ cells. Mean follow-up was 29.3 ± 16 months. We evaluated SR as well as VE. Patients were classified as to the presence or absence of EPC in the circulation (either EPC+ or EPC-). Bivariate analyses, Kaplan-Meier survival curves and Cox regression models were used.ResultsWe included 121 patients (mean age 70.1±12.6 years; 65% were men). The percentage of EPC+ patients was 47.1%. SR occurred in 12 (9.9%) and VE in 18 (14.9%) patients. SR was associated significantly with a worse prior RS score, previous stroke and etiology, but not with EPC count. VE were associated significantly with EPC-, worse prior RS score, previous stroke, high age, peripheral artery disease and etiology. Cox regression model showed that EPC- (HR 7.07, p=0.003), age (HR 1.08, p=0.004) and a worse prior RS score (HR 5.8, p=0.004) were associated significantly with an increased risk of VE.ConclusionsThe absence of circulating EPC is not associated with the risk of stroke recurrence, but is associated with an increased risk of future vascular events.

Highlights

  • Circulating endothelial progenitor cells (EPC) were described in 1997 by Asahara et al[1]

  • We evaluated the hypothesis that the number of circulating EPC could be associated with the risk of stroke recurrence (SR) or vascular events (VE) after an ischemic stroke

  • Cox regression model showed that EPC- (HR 7.07, p=0.003), age (HR 1.08, p=0.004) and a worse prior Rankin scale (RS) score (HR 5.8, p=0.004) were associated significantly with an increased risk of VE

Read more

Summary

Introduction

Circulating endothelial progenitor cells (EPC) were described in 1997 by Asahara et al[1]. EPC are immature endothelial circulating cells mobilized from the bone marrow that are released into the bloodstream. These cells have an essential physiologic role in vascular homeostasis: they are necessary to repair the injured endothelium and to enable neovascularization after ischemia[2,3,4,5,6]. It is likely that low counts of EPC may produce vascular events due to the inability of EPC to perform their physiological role In agreement with this reasoning, two studies[8,9] in patients with coronary artery disease found that EPC counts predicted the occurrence of cardiovascular events during follow-up. We evaluated the hypothesis that the number of circulating EPC could be associated with the risk of stroke recurrence (SR) or vascular events (VE) after an ischemic stroke

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call