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缺血性卒中患者血浆 fractalkine 水平的时间动态变化:与临床严重程度及预后的关联

The temporal dynamics of plasma fractalkine levels in ischemic stroke: association with clinical severity and outcome.

作者信息

Grosse Gerrit M, Tryc Anita B, Dirks Meike, Schuppner Ramona, Pflugrad Henning, Lichtinghagen Ralf, Weissenborn Karin, Worthmann Hans

机构信息

Department of Neurology, Hannover Medical School, Carl-Neuberg-Str, 1, 30625 Hannover, Germany.

出版信息

J Neuroinflammation. 2014 Apr 10;11:74. doi: 10.1186/1742-2094-11-74.

Abstract

BACKGROUND

The chemokine fractalkine (CX3CL1, FKN) is involved in neural-microglial interactions and is regarded as neuroprotective according to several in vivo studies of inflammatory and degenerative states of the brain. Recently, an association with outcome in human ischemic stroke has been proposed. In this study, we aimed to investigate the temporal pattern of FKN levels in acute ischemic stroke in relation to stroke severity and outcome.

METHODS

FKN levels were measured in plasma specimens of fifty-five patients with acute ischemic stroke. Blood was available for time points 6 hours (h), 12 h, 3 days (d), 7 d and 90 d after stroke onset. Clinical outcome was evaluated using the modified Rankin Scale (mRS) at 7 d and 90 d.

RESULTS

The time course of FKN significantly differs depending on stroke severity, with higher FKN levels linked to a lower severity. FKN levels in patients with moderate to severe strokes differ significantly from controls. In outcome analysis, we found an association of dynamics of FKN with clinical outcome. Decrease of FKN is pronounced in patients with worse outcome. Multivariate analysis including stroke severity and stroke etiology revealed that deltaFKN between 6 h and 3 d is independently associated with mRS at 90 d. In addition deltaFKN is inversely correlated with the extent of brain damage, as measured by S100B.

CONCLUSIONS

FKN dynamics are independently associated with stroke outcome. Further studies might give insight on whether FKN is actively involved in the inflammatory cascade after acute ischemic stroke.

摘要

背景

趋化因子fractalkine(CX3CL1,FKN)参与神经-小胶质细胞相互作用,并且根据几项关于脑炎症和退行性状态的体内研究被认为具有神经保护作用。最近,有人提出其与人类缺血性卒中的预后有关。在本研究中,我们旨在调查急性缺血性卒中患者FKN水平的时间模式及其与卒中严重程度和预后的关系。

方法

检测了55例急性缺血性卒中患者血浆样本中的FKN水平。在卒中发作后6小时(h)、12小时、3天(d)、7天和90天的时间点可获取血液样本。在第7天和第90天使用改良Rankin量表(mRS)评估临床预后。

结果

FKN的时间进程因卒中严重程度而异,FKN水平越高,严重程度越低。中度至重度卒中患者的FKN水平与对照组有显著差异。在预后分析中,我们发现FKN的动态变化与临床预后有关。预后较差的患者FKN下降明显。包括卒中严重程度和卒中病因的多变量分析显示,6小时至3天之间的FKN变化量(deltaFKN)与90天时的mRS独立相关。此外,deltaFKN与通过S100B测量的脑损伤程度呈负相关。

结论

FKN动态变化与卒中预后独立相关。进一步的研究可能有助于了解FKN是否积极参与急性缺血性卒中后的炎症级联反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e553/4022085/32234009fed6/1742-2094-11-74-1.jpg

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