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Decrease in endothelial progenitor cells associated with inflammation, but not with endothelial dysfunction in chronic hemodialysis patients

机译:慢性血液透析患者中​​与炎症有关的内皮祖细胞减少,但与内皮功能障碍无关

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Introduction: Endothelial progenitor cells (EPC), bone marrow derived cells, are considered to have a pivotal role in maintaining the integrity and repair of the endothelium. Endothelial dysfunction, atherosclerosis and inflammation are implicated for increased CV mortality in uremia. In this study, we aimed to investigate the possible association of EPC with inflammation, endothelial dysfunction and atherosclerosis in chronic hemodialysis (HD) patients. Patients and methods: 67 HD patients (male/female: 30/37, mean age: 58 ± 15 years) and 22 healthy controls (male/female: 13/9; mean age: 48 ± 8 years) were included. EPC were cultivated in the fibronectin-covered culture dishes and counted. Also EPC markers were studied by flow cytometry using anti-CD34, anti-CD133 and anti-vascular endothelial growth factor receptor 2 (VEGFR-2) antibodies. Serum levels of IL-6, TNF-a, intercellular cell adhesion molecule (ICAM), vascular cell adhesion molecule (VCAM) and asymmetric dimethyl-arginine (ADMA) were measured by ELISA method. Endothelial function was investigated by measuring flow-mediated dilatation (FMD) of the brachial artery. Carotid intima-media thickness (CIMT) and ratio (CIMR) were also examined. Results: EPC number was decreased in HD patients when compared to controls (63.7 ± 8.9 vs. 101.5 ± 19.6/ high power field, p 0.001). Also CD34+ cell count was significantly lower in the HD group (2.26 ± 3.52 vs. 6.03 ± 4.73%, p 0.0001). EPC number was significantly inversely correlated with serum TNF-a levels in HD patients(r: -0.453, p 0.001) and also in the control group (r = -0.509, p = 0.044). There was an inverse association between VEGFR-2+/CD34+cell count and serum IL-6 levels (r: -0.364, p = 0.006) in HD patients. However, EPC count was not related to FMD and CIMT/CIMR. In HD patients, there was a positive correlation between serum IL-6 levels with CIMT (r = 0.358, p = 0.01) and CIMR was positively correlated with serum ICAM (r = 0.430, p = 0.002). Conclusion: EPC number was decreased in uremia and was associated with inflammation. TNF-a might have specific inhibitory actions on EPC in both HD patients and healthy controls. No relationship was present between EPC and endothelial dysfunction/atherosclerosis
机译:简介:内皮祖细胞(EPC)是骨髓来源的细胞,被认为在维持内皮的完整性和修复中起着关键作用。内皮功能障碍,动脉粥样硬化和炎症与尿毒症的CV死亡率增加有关。在这项研究中,我们旨在调查EPC与慢性血液透析(HD)患者的炎症,内皮功能障碍和动脉粥样硬化的可能联系。患者和方法:包括67名HD患者(男性/女性:30/37,平均年龄:58±15岁)和22名健康对照(男性/女性:13/9;平均年龄:48±8岁)。 EPC在覆盖有纤连蛋白的培养皿中培养并计数。还使用抗CD34,抗CD133和抗血管内皮生长因子受体2(VEGFR-2)抗体通过流式细胞术研究了EPC标记。通过ELISA法测定血清中IL-6,TNF-α,细胞间细胞粘附分子(ICAM),血管细胞粘附分子(VCAM)和不对称二甲基精氨酸(ADMA)的水平。通过测量肱动脉的血流介导的扩张(FMD)来研究内皮功能。还检查了颈动脉内膜中层厚度(CIMT)和比率(CIMR)。结果:与对照组相比,HD患者的EPC数量减少(63.7±8.9与101.5±19.6 /高倍视野,p <0.001)。 HD组的CD34 +细胞计数也显着降低(2.26±3.52 vs. 6.03±4.73%,p <0.0001)。 HD患者中EPC值与血清TNF-α水平呈显着负相关(r:-0.453,p <0.001),而对照组(r = -0.509,p = 0.044)。 HD患者的VEGFR-2 + / CD34 +细胞计数与血清IL-6水平呈负相关(r:-0.364,p = 0.006)。但是,EPC计数与FMD和CIMT / CIMR无关。在HD患者中,血清IL-6水平与CIMT呈正相关(r = 0.358,p = 0.01),而CIMR与血清ICAM呈正相关(r = 0.430,p = 0.002)。结论:尿毒症患者的EPC数量减少,并与炎症有关。 TNF-α对HD患者和健康对照者均具有对EPC的特异性抑制作用。 EPC与内皮功能障碍/动脉粥样硬化之间没有关系

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