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Dynamic changes in peripheral blood-targeted miRNA expression profiles in patients with severe traumatic brain injury at high altitude

机译:高海拔严重创伤性脑损伤患者外周血靶向miRNA表达谱的动态变化

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The aim of this work is to detect and compare the peripheral blood miRNA expression profiles in patients with severe traumatic brain injury (sTBI) 2, 12, 24, 48, and 72?h after injury at high altitude and to predict the target genes of differential expressed miRNAs. Twenty sTBI patients from high-altitude areas were randomly selected according to the inclusion and exclusion criteria and were divided into five groups: the 2-h group, 12-h group, 24-h group, 48-h group, and 72-h group. Peripheral blood miRNA expression profiles were detected using real-time quantitative PCR (qRT-PCR). The expression levels of miR-18a, miR-203, miR-146a, miR-149, miR-23b, and miR-let-7b in peripheral blood showed significant differences between the 2-h group and the 12-h group. The expression levels of miR-203, miR-146a, miR-149, miR-23b, and miR-let-7f in peripheral blood were up-regulated in the 24-h group. In the 48-h group, the expression levels of miR-181d, miR-29a, and miR-18b were upregulated. In the 72-h group, the expression levels of miR-203, miR-146a, miR-149, miR-23b, and miR-let-7f changed. The main target genes of the differentiation expressed miRNAs were genes that regulate inflammatory responses, apoptosis, and DNA damage/repair. miRNAs may be involved in the pathogenesis of sTBI by dynamically regulating the target genes that regulate inflammatory responses, apoptosis, and DNA damage/repair pathways.
机译:这项工作的目的是检测和比较在高海拔损伤后严重创伤性脑损伤(STBI)2,12,24,48和72ΩH的患者外周血miRNA表达曲线,并预测靶基因差异表达的miRNA。根据夹杂物和排斥标准随机选择来自高空区域的二十次STBI患者,分为五组:2-H组,12-H组,24小时,48小时,72-H.团体。使用实时定量PCR(QRT-PCR)检测外周血miRNA表达谱。外周血中miR-18a,miR-203,miR-146a,miR-149,miR-23b和miR-let-7b的表达水平显示出2-h组和12-h组之间的显着差异。 MiR-203,miR-146a,miR-149,miR-23b和miR-let-7f的表达水平在24小时组中升压。在48-H组中,MiR-181D,miR-29a和miR-18b的表达水平被上调。在72-H组中,miR-203,miR-146a,miR-149,miR-23b和miR-let-7f的表达水平改变。分化表达的miRNA的主要靶基因是调节炎症反应,细胞凋亡和DNA损伤/修复的基因。通过动态调节调节炎症反应,细胞凋亡和DNA损伤/修复途径的靶基因,MIRNA可以参与STBI的发病机制。

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