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用于确定动脉瘤性蛛网膜下腔出血后迟发性脑血管痉挛风险的高度预测性微小RNA检测板

A Highly Predictive MicroRNA Panel for Determining Delayed Cerebral Vasospasm Risk Following Aneurysmal Subarachnoid Hemorrhage.

作者信息

Wang Wang-Xia, Springer Joe E, Xie Kevin, Fardo David W, Hatton Kevin W

机构信息

Sanders Brown Center on Aging, University of Kentucky, Lexington, KY, United States.

Spinal Cord and Brain Injury Research Center, University of Kentucky, Lexington, KY, United States.

出版信息

Front Mol Biosci. 2021 May 14;8:657258. doi: 10.3389/fmolb.2021.657258. eCollection 2021.

Abstract

Approximately one-third of aneurysmal subarachnoid hemorrhage (aSAH) patients develop delayed cerebral vasospasm (DCV) 3-10 days after aneurysm rupture resulting in additional, permanent neurologic disability. Currently, no validated biomarker is available to determine the risk of DCV in aSAH patients. MicroRNAs (miRNAs) have been implicated in virtually all human diseases, including aSAH, and are found in extracellular biofluids including plasma and cerebrospinal fluid (CSF). We used a custom designed TaqMan Low Density Array miRNA panel to examine the levels of 47 selected brain and vasculature injury related miRNAs in CSF and plasma specimens collected from 31 patients with or without DCV at 3 and 7 days after aSAH, as well as from eight healthy controls. The analysis of the first 18-patient cohort revealed a striking differential expression pattern of the selected miRNAs in CSF and plasma of aSAH patients with DCV from those without DCV. Importantly, this differential expression was observed at the early time point (3 days after aSAH), before DCV event occurs. Seven miRNAs were identified as reliable DCV risk predictors along with a prediction model constructed based on an array of additional 19 miRNAs on the panel. These chosen miRNAs were then used to predict the risk of DCV in a separate, testing cohort of 15 patients. The accuracy of DCV risk prediction in the testing cohort reached 87%. The study demonstrates that our novel designed miRNA panel is an effective predictor of DCV risk and has strong applications in clinical management of aSAH patients.

摘要

大约三分之一的动脉瘤性蛛网膜下腔出血(aSAH)患者在动脉瘤破裂后3 - 10天会发生迟发性脑血管痉挛(DCV),导致额外的永久性神经功能障碍。目前,尚无经过验证的生物标志物可用于确定aSAH患者发生DCV的风险。微小RNA(miRNA)几乎涉及所有人类疾病,包括aSAH,并且存在于细胞外生物流体中,包括血浆和脑脊液(CSF)。我们使用定制设计的TaqMan低密度阵列miRNA检测板,检测了31例aSAH患者(有或无DCV)在aSAH后3天和7天采集的脑脊液和血浆样本以及8名健康对照中47种选定的与脑和血管损伤相关的miRNA的水平。对首批18例患者队列的分析显示,有DCV的aSAH患者与无DCV的患者相比,其脑脊液和血浆中选定的miRNA存在显著的差异表达模式。重要的是,这种差异表达在DCV事件发生前的早期时间点(aSAH后3天)就已观察到。7种miRNA被确定为可靠的DCV风险预测指标,并基于检测板上另外19种miRNA构建了一个预测模型。然后将这些选定的miRNA用于预测另外15例患者组成的独立测试队列中DCV的风险。测试队列中DCV风险预测的准确率达到了87%。该研究表明,我们新设计的miRNA检测板是DCV风险的有效预测指标,在aSAH患者的临床管理中有很强的应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1647/8163224/cf9b95cfbd1e/fmolb-08-657258-g001.jpg

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