Modak Janhavi M, Roy-O'Reilly Meaghan, Zhu Liang, Staff Ilene, McCullough Louise D
Department of Neurology, Hartford Hospital, Hartford, Connecticut.
Department of Neurology, University of Texas Health Science Center, Houston, Texas.
J Stroke Cerebrovasc Dis. 2019 Jan;28(1):121-124. doi: 10.1016/j.jstrokecerebrovasdis.2018.09.018. Epub 2018 Oct 11.
MicroRNAs (miRNA) are a class of small, endogenous (17-25 nucleotide) noncoding ribonucleic acids implicated in the transcriptional and post-transcriptional regulation of gene expression. This study examines stroke-specific miRNA expression in large vessel territory cardioembolic stroke.
Peripheral blood was collected from controls and ischemic stroke patients 24 hours after stroke onset. Whole blood miRNA was isolated and analyzed for differential expression. A total of 16 patients with acute middle cerebral artery territory strokes of cardioembolic origin were included in this pilot study. MiRNA profiling was conducted by miRCURY LNA™ microRNA Array.
In patients with cardioembolic stroke, significant differential expression of 14 miRNAs was observed when compared to controls. Ten of these miRNA had not previously been associated with ischemic stroke (miR-664a-3p, -2116-5pp, -4531, -4765-5p, -647, -4709-3p, -4742-3p, -5584-3p, -4756-3p, and -5187-3p). Subanalysis of severe strokes (NIHSS > 10) identified an additional 5 differentially expressed miRNA. No significant effects of sex or tissue plasminogen activator treatment were seen on miRNA expression.
Ischemic stroke patients show a differential miRNA expression profile as compared to controls. These new associations between circulating miRNAs and ischemic stroke may help to refine stroke subtype diagnosis and identify novel therapeutic miRNA targets for the treatment of ischemic stroke.
微小RNA(miRNA)是一类小的内源性(17 - 25个核苷酸)非编码核糖核酸,参与基因表达的转录和转录后调控。本研究检测大动脉区域心源性栓塞性卒中特异性miRNA的表达。
在卒中发作后24小时从对照组和缺血性卒中患者采集外周血。分离全血miRNA并分析其差异表达。本初步研究共纳入16例急性大脑中动脉区域心源性栓塞性卒中患者。通过miRCURY LNA™微小RNA阵列进行miRNA谱分析。
与对照组相比,在心源性栓塞性卒中患者中观察到14种miRNA有显著差异表达。其中10种miRNA此前未与缺血性卒中相关联(miR - 664a - 3p、- 2116 - 5pp、- 4531、- 4765 - 5p、- 647、- 4709 - 3p、- 4742 - 3p、- 5584 - 3p、- 4756 - 3p和- 5187 - 3p)。对严重卒中(美国国立卫生研究院卒中量表评分>10)的亚分析又鉴定出5种差异表达的miRNA。未观察到性别或组织纤溶酶原激活剂治疗对miRNA表达有显著影响。
与对照组相比,缺血性卒中患者表现出不同的miRNA表达谱。循环miRNA与缺血性卒中之间的这些新关联可能有助于完善卒中亚型诊断,并确定用于治疗缺血性卒中的新的治疗性miRNA靶点。