Reduced Number of Circulating Endothelial Progenitor Cells (CD133+/KDR+) in Patients with Plaque Psoriasis

被引:22
作者
Batycka-Baran, Aleksandra [1 ]
Paprocka, Maria [2 ]
Krawczenko, Agnieszka [2 ]
Kantor, Aneta [2 ]
Dus, Danuta [2 ]
Szepietowski, Jacek C. [1 ]
机构
[1] Wroclaw Med Univ, Dept Dermatol Venereol & Allergol, PL-50368 Wroclaw, Poland
[2] Polish Acad Sci, Inst Immunol & Expt Therapy, PL-53114 Wroclaw, Poland
关键词
Circulating endothelial progenitor cells; Psoriasis; Endothelial dysfunction; Atherosclerosis; Cardiovascular risk; TNF-ALPHA; THERAPY; ATHEROSCLEROSIS; CORRELATE; DISEASES; SERUM;
D O I
10.1159/000341534
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
Background: Psoriasis is associated with an increased cardiovascular risk. Circulating endothelial progenitor cells (CEPCs) play a significant role in the maintenance of vascular homeostasis. Objective: The aim of this study was to evaluate the number of CEPCs in patients with psoriasis compared to controls and assess possible correlations between the number of these cells and the plasma levels of vascular endothelial growth factor (VEGF), soluble vascular endothelial growth factor receptor-1 (sVEGFR-1) and clinical features of psoriasis. Methods: The number of CEPCs, identified as CD133+/KDR+ cells, was determined with flow cytometry in peripheral blood of psoriatic patients (n = 63) and controls (n = 31). The plasma levels of VEGF and sVEGFR-1 were measured with enzyme-linked immunosorbent assay. Results: The number of CEPCs was significantly reduced in psoriatic patients compared with controls (p = 0.000026) and inversely correlated with disease severity (R = -0.283; p = 0.0248). Conclusion: A reduced number of CEPCs may contribute to endothelial dysfunction in patients with psoriasis. Copyright (C) 2012 S. Karger AG, Basel
引用
收藏
页码:88 / 92
页数:5
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