Acute ischemic stroke: how to investigate the association between disease etiology and gene expression profiles

Giulia Cassioli, Ada Kura, A. Sodero, E. Sticchi, A. Magi, Samuele Suraci, Rosina De Cario, A. Consoli, A. Rosi, S. Nappini, L. Renieri, N. Limbucci, Benedetta Piccardi, F. Arba, C. Sarti, D. Inzitari, S. Mangiafico, R. Marcucci, A. Gori, B. Giusti
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Abstract

Background: Acute ischemic stroke (AIS) represents one of the principal causes of neurological morbidity and mortality worldwide. For a prompt and efficient cerebral blood restoration, intravenous treatment with rt-PA is often combined with mechanical thrombectomy (MT) which provides cerebral thrombi (CT) as study material, allowing the investigation of its cellular composition, morphological and histopathological features. Indeed, the determination of stroke etiology, typically defined by the TOAST classification, is paramount for prognostic factors, outcome, and management of the event. Aim of the study is therefore to highlight and analyze gene expression profiles in thrombotic tissue and peripheral blood (PB) in the comparison between strokes of cardioembolic (CE) and atherosclerotic (LAA) origin. Methods: We performed gene expression profiles of 92 patients. CT were stored in RNA later and RNA was extracted by PAX gene blood miRNA kit. The global gene expression profile was assessed by Affymetrix technology using GeneChip Human Transcriptome Array 2.0 combined with Affymetrix Transcriptome Analysis Console (TAC) Software. Results: Currently, we focused our attention on CT data analysis. The analysis revealed a significant difference (p-value<0.05 and FoldChange=2 as threshold) in gene expression when comparing LAA and CE stroke. In particular, from CT of atherosclerotic origin emerges an overexpression of 1766 genes. Prominent among them are genes such as MMP-9, TGFB, TGFBR and CXCL1, primarily involved in neutrophil-mediated immunity, Blood-Brain Barrier (BBB) disruption processes, and associated with atherosclerotic plaque instability and related to poor neurological outcome, suggesting a deleterious role in human brain injury. As concerns CE patients, 57 genes mainly involved in transcriptional regulatory processes turn out to be significantly overexpressed. Conclusions: Transcriptome profiling is a powerful weapon for revealing expression patterns associated with complex disorders. The variation of gene expression profiles confirmed and extended several known pathophysiological mechanisms and may be one way of delineating different stroke etiology.
急性缺血性脑卒中:如何研究疾病病因与基因表达谱之间的关系
背景:急性缺血性脑卒中(AIS)是世界范围内神经系统发病和死亡的主要原因之一。为了迅速有效地恢复脑血,静脉注射rt-PA治疗通常与机械取栓术(MT)相结合,后者提供脑血栓(CT)作为研究材料,可以研究其细胞组成、形态和组织病理学特征。事实上,卒中病因的确定,通常由TOAST分类定义,对于预后因素、结果和事件管理至关重要。因此,该研究的目的是强调和分析血栓组织和外周血(PB)中的基因表达谱,比较心脏栓塞(CE)和动脉粥样硬化(LAA)起源的中风。方法:对92例患者进行基因表达谱分析。CT后保存于RNA中,用PAX基因血miRNA试剂盒提取RNA。使用GeneChip Human Transcriptome Array 2.0结合Affymetrix转录组分析控制台(TAC)软件,采用Affymetrix技术评估全局基因表达谱。结果:目前,我们主要关注CT数据分析。分析结果显示,LAA与CE卒中患者基因表达差异有统计学意义(p值<0.05,FoldChange=2为阈值)。特别是,动脉粥样硬化起源的CT显示1766个基因过表达。其中突出的是MMP-9、TGFB、TGFBR和CXCL1等基因,它们主要参与中性粒细胞介导的免疫、血脑屏障(BBB)破坏过程,与动脉粥样硬化斑块不稳定相关,并与不良的神经预后相关,表明它们在人脑损伤中具有有害作用。在CE患者中,有57个主要参与转录调控过程的基因显著过表达。结论:转录组分析是揭示与复杂疾病相关的表达模式的有力武器。基因表达谱的变化证实并扩展了几种已知的病理生理机制,可能是描述不同中风病因的一种方法。
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