Clinica Medica, Department of Medical and Surgical Sciences, University of Brescia, Spedali Civili, 25100 Brescia, Italy.
J Endocrinol Invest. 2011 May;34(5):335-9. doi: 10.1007/BF03347455. Epub 2010 Jun 28.
A relevant biological role of circulating endothelial progenitor cells (EPC) was recently demonstrated. EPC are generated in the bone marrow, and interact with damaged endothelium, restoring the integrity of the monolayer. Therefore, aim of the present study was to evaluate EPC in the blood of patients with untreated Graves' hyperthyroidism (GD), in whom an increased oxidative stress was observed.
Twenty-three patients with untreated active GD and 18 matched normal controls (NC) were included in the study. Circulating EPC were isolated from peripheral blood. Mononuclear cells were cultured with endothelial basal medium supplemented with EGM SingleQuots, and were identified by positive double staining after 7 days in culture. Circulating levels of C reactive protein, total antioxidant power, interleukin (IL)-6, IL- 18, monocyte chemoattractant protein-1, tumor necrosis facotr- α, soluble vascular cell adhesion molecule (VCAM) and intracellular adhesion molecule were evaluated by enzymelinked immunosorbent assay kit. EPC number was also evaluated in a subgroup of GD patients after restoration of euthyroidism.
Systolic blood pressure resulted increased in GD patients compared with control subjects whereas diastolic blood pressure was not significantly different. Patients with GD showed an increase in circulating levels of IL-18 and VCAM-1 and a reduction of total antioxidant power (p<0.05) compared to NC. Moreover, a reduced number of EPC was observed in patients with GD compared to NC (p<0.05) which turned to NC values after restoring euthyroidism.
Patients with GD showed a reduction in the physiological protective mechanisms against endothelial damage, probably induced by increased inflammation and oxidative stress.
最近发现循环内皮祖细胞(EPC)具有相关的生物学作用。EPC 于骨髓中生成,并与受损的内皮相互作用,恢复单层内皮的完整性。因此,本研究旨在评估未经治疗的格雷夫斯甲亢(GD)患者血液中的 EPC,这些患者观察到氧化应激增加。
本研究纳入了 23 例未经治疗的活动期 GD 患者和 18 例匹配的正常对照组(NC)。从外周血中分离循环 EPC。单核细胞在补充有 EGM SingleQuots 的内皮基础培养基中培养,培养 7 天后通过阳性双重染色进行鉴定。通过酶联免疫吸附试剂盒评估循环 C 反应蛋白、总抗氧化能力、白细胞介素(IL)-6、IL-18、单核细胞趋化蛋白-1、肿瘤坏死因子-α、可溶性血管细胞黏附分子(VCAM)和细胞间黏附分子的水平。在 GD 患者恢复甲状腺功能正常后,还评估了 EPC 数量。
与对照组相比,GD 患者的收缩压升高,而舒张压无明显差异。与 NC 相比,GD 患者的循环 IL-18 和 VCAM-1 水平升高,总抗氧化能力降低(p<0.05)。此外,与 NC 相比,GD 患者的 EPC 数量减少(p<0.05),在恢复甲状腺功能正常后恢复至 NC 值。
GD 患者对内皮损伤的生理保护机制减少,这可能是由炎症和氧化应激增加引起的。