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Circulating endothelial progenitor cells and endothelial cells in moyamoya disease

INTRODUCTION: There is no well‐recognized biomarker for accurately predicting outcome in the presence of moyamoya disease (MMD), a progressive occlusive cerebrovascular disease of the internal carotid arteries or their branches. The aim of this study was to investigate the presence of endothelial pr...

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Detalles Bibliográficos
Autores principales: Bao, Xiang‐Yang, Fan, Yan‐Na, Liu, Yi, Wang, Qian‐Nan, Zhang, Yong, Zhu, Bing, Liu, Bing, Duan, Lian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160662/
https://www.ncbi.nlm.nih.gov/pubmed/30141248
http://dx.doi.org/10.1002/brb3.1035
Descripción
Sumario:INTRODUCTION: There is no well‐recognized biomarker for accurately predicting outcome in the presence of moyamoya disease (MMD), a progressive occlusive cerebrovascular disease of the internal carotid arteries or their branches. The aim of this study was to investigate the presence of endothelial progenitor cells (EPCs) and circulating endothelial cells (CECs) in MMD and correlate the findings with clinical features. METHODS: Patients with MMD (n = 66) were compared with healthy controls (n = 81). Blood samples were obtained from an antecubital vein and analyzed using flow cytometry. EPCs were defined as CD31(+) CD45(dim) CD34(br) CD133(+) and CECs as CD31(br) CD45(−) CD34(dim) CD133(−). Univariate and multivariate linear regression analyses were carried out. RESULTS: The CEC counts were significantly higher in the patients than in the controls (p = 0.008). In multivariate analysis, EPC counts were independently associated with age of patients with MMD (p = 0.049) and CEC counts were independently negatively associated with concomitant disease such as hypertension, diabetes mellitus, and coronary heart disease (p = 0.034). CONCLUSIONS: This is the first study to investigate the presence of CECs in the plasma of patients with MMD, and the amount of CECs was negatively correlated with concomitant disease in these patients.