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在早期缺血性脑卒中患者中,循环 CD133+CD34+祖细胞与可溶性细胞间黏附分子-1 呈负相关。

Circulating CD133+CD34+ progenitor cells inversely correlate with soluble ICAM-1 in early ischemic stroke patients.

机构信息

Stroke Diagnostics and Therapeutics Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892-1401, USA.

出版信息

J Transl Med. 2011 Aug 26;9:145. doi: 10.1186/1479-5876-9-145.

Abstract

BACKGROUND AND PURPOSE

Both endothelial progenitor cells (EPC) and markers of neuroinflammation are candidate biomarkers for stroke severity and outcome prediction. A relationship between EPC and neuroinflammatory markers in early stroke is not fully elucidated. The objectives were to investigate correlations between EPC and neuroinflammation markers (adhesion molecules ICAM-1, VCAM-1, E-selectin, tumor necrosis factor (TNF)-α, interleukin (IL)-6, endothelin (ET)-1, markers of tissue injury (matrix metalloproteinases (MMP)-9 and tissue inhibitor of matrix metalloproteinases (TIMP)-1) in early stroke patients.

METHODS

We prospectively recruited symptomatic patients with ischemic cerebrovascular disease. We assessed stroke severity by using of acute (diffusion-weighted imaging (DWI) and final lesion volumes (fluid attenuated inversion recovery (FLAIR). We measured serum soluble ICAM-1, VCAM-1, E-selectin, MMP-9, TIMP-1 and plasma TNF-α, IL-6, ET-1 by ELISA, and quantified EPC in mononuclear fraction of peripheral blood on days 1 and 3 in 17 patients (mean(SD) age 62(14), with admission National Institutes of Health Stroke Scale (NIHSS) 10(8)) selected from 175 patients with imaging confirmed ischemic stroke. Non-parametric statistics, univariate and multivariate analysis were used.

RESULTS

Only ICAM-1 inversely correlated with EPC subset CD133+CD34+ on day 1 (Spearman r = -0.6, p < 0.01) and on day 3 (r = -0.967, p < 0.001). This correlation remained significant after adjustment for age and NIHSS (beta -0.992, p < 0.004), for glucose and systolic blood pressure (beta -0.86, p < 0.005), and for white blood cells and hematocrit (beta -1.057, p < 0.0001) on day 3. MMP-9 (r = 0.509, p < 0.04) and MMP-9/TIMP-1 (r = 0.59, p < 0.013) on day 1 correlated with acute lesion volume. Both IL-6 (r = 0.624, p < 0.01) and MMP-9/TIMP-1 (r = 0.56, p < 0.02) correlated with admission NIHSS.

CONCLUSION

Our study showed that high ICAM-1 is associated with low CD133+CD34+subset of EPC. Biomarkers of neuroinflammation may predict tissue injury and stroke severity in early ischemia.

摘要

背景与目的

内皮祖细胞(EPC)和神经炎症标志物都是卒中严重程度和预后预测的候选生物标志物。EPC 与早期卒中的神经炎症标志物之间的关系尚未完全阐明。本研究旨在探讨早期卒中患者 EPC 与神经炎症标志物(黏附分子 ICAM-1、VCAM-1、E-选择素、肿瘤坏死因子(TNF)-α、白细胞介素(IL)-6、内皮素(ET)-1、组织损伤标志物(基质金属蛋白酶(MMP)-9 和基质金属蛋白酶组织抑制剂(TIMP)-1)之间的相关性。

方法

我们前瞻性招募了有症状的缺血性脑血管病患者。采用急性弥散加权成像(DWI)和最终病灶体积(FLAIR)评估卒中严重程度。通过酶联免疫吸附试验(ELISA)测量血清可溶性 ICAM-1、VCAM-1、E-选择素、MMP-9、TIMP-1 和血浆 TNF-α、IL-6、ET-1,在 175 例影像学证实的缺血性卒中患者中选择 17 例(平均年龄 62(14)岁,入院 NIHSS 评分为 10(8)分),于第 1 天和第 3 天测量外周血单核细胞中 EPC。采用非参数统计、单变量和多变量分析。

结果

仅 ICAM-1 与第 1 天(Spearman r = -0.6,p < 0.01)和第 3 天(r = -0.967,p < 0.001)的 EPC 亚群 CD133+CD34+呈负相关。校正年龄和 NIHSS(β-0.992,p < 0.004)、血糖和收缩压(β-0.86,p < 0.005)以及第 3 天白细胞和红细胞压积(β-1.057,p < 0.0001)后,这种相关性仍然显著。第 1 天 MMP-9(r = 0.509,p < 0.04)和 MMP-9/TIMP-1(r = 0.59,p < 0.013)与急性病灶体积相关。第 1 天的 IL-6(r = 0.624,p < 0.01)和 MMP-9/TIMP-1(r = 0.56,p < 0.02)与入院 NIHSS 相关。

结论

本研究表明,高 ICAM-1 与 CD133+CD34+EPC 亚群减少有关。神经炎症标志物可能预测早期缺血性组织损伤和卒中严重程度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2fc/3179728/d22c32d5c271/1479-5876-9-145-1.jpg

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