Unit of Metabolic Diseases, Department of Geriatrics and Metabolic Diseases, Second University of Naples, Naples, Italy.
J Endocrinol Invest. 2013 Nov;36(10):825-30. doi: 10.3275/9020. Epub 2013 Jun 26.
Endothelial progenitor cells (EPCs), involved in the repairing mechanisms of vascular damage, are positively correlated to insulin-like growth factor I (IGF-I) concentrations in healthy adults. However, the levels of EPCs and their role in acromegalic patients have never been investigated.
We conducted a cross-sectional study in order to assess the levels of the different phenotypes of circulating EPC in acromegalic patients.
The study was performed at the Endocrinology Unit of Federico II University and at the Unit of Metabolic Diseases and Endocrinology of the Second University of Naples. Fifty-five acromegalic patients and 65 healthy controls were studied. EPCs were assessed by flow cytometry and IGF-I by immunoradiometric assay.
Compared with subjects of the control group, acromegalic patients showed significantly higher levels of EPCs phenotypes expressing KDR antigen [KDR+, cells per 106 events, median and interquartile range, 44 (28-67) vs 23 (13-40), p=0.006; CD34+KDR+ 25 (18-38) vs 12 (8-17), p<0.001; CD133+KDR+ 17 (13-30) vs 8 (6-12), p<0.001; CD34+KDR+CD133+ 16 (12-25) vs 8 (6-10), p<0.001]. There was a positive correlations between CD34+KDR+CD133+ cells count and IGF-I in acromegaly group (r=0.79, p<0.001).
Acromegalic patients show higher circulating EPCs levels expressing KDR, positively correlated with IGF-I, suggesting a role for IGF-I in regulating the expression of this surface marker in the early phase of EPCs differentiation.
参与血管损伤修复机制的内皮祖细胞(EPCs)与健康成年人的胰岛素样生长因子 I(IGF-I)浓度呈正相关。然而,EPCs 的水平及其在肢端肥大症患者中的作用从未被研究过。
我们进行了一项横断面研究,以评估肢端肥大症患者循环 EPC 的不同表型水平。
该研究在那不勒斯第二大学代谢疾病和内分泌学系的内分泌学单位进行。研究了 55 例肢端肥大症患者和 65 例健康对照者。通过流式细胞术评估 EPCs,通过免疫放射测定法评估 IGF-I。
与对照组受试者相比,肢端肥大症患者表达 KDR 抗原的 EPCs 表型水平显著升高[KDR+,每 106 个事件中的细胞数,中位数和四分位距,44(28-67)比 23(13-40),p=0.006;CD34+KDR+25(18-38)比 12(8-17),p<0.001;CD133+KDR+17(13-30)比 8(6-12),p<0.001;CD34+KDR+CD133+16(12-25)比 8(6-10),p<0.001]。肢端肥大症组 CD34+KDR+CD133+细胞计数与 IGF-I 呈正相关(r=0.79,p<0.001)。
肢端肥大症患者表现出更高水平的表达 KDR 的循环 EPCs,与 IGF-I 呈正相关,这表明 IGF-I 在调节 EPCs 分化早期这种表面标志物的表达中起作用。