Department of Neurology, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People's Hospital, Shenzhen 518000, China.
Research and Development Unit, Shenzhen GenDo Medical Technology Co., Ltd., Dapeng, Shenzhen 518000, China.
Int J Med Sci. 2023 Jun 4;20(8):1009-1023. doi: 10.7150/ijms.83963. eCollection 2023.
Ischemic stroke (IS) is the majority of strokes which remain the second leading cause of deaths in the last two decades. Circulating microRNAs (miRNAs) have been suggested as potential diagnostic and therapeutic tools for IS by previous studies analyzing their differential expression. However, inconclusive and controversial conclusions of these results have to be addressed. In this study, comprehensive analysis and real-world validation were performed to assess the associations between circulating miRNAs and IS. 29 studies with 112 miRNAs were extracted after manual selection and filtering, 12 differentially expressed miRNAs were obtained from our results of meta-analysis. These miRNAs were evaluated in 20 IS patients, compared to 20 healthy subjects. 4 miRNAs (hsa-let-7e-5p, hsa-miR-124-3p, hsa-miR-17-5p, hsa-miR-185-5p) exhibited the significant expression level in IS patient plasma samples. Pathway and biological process enrichment analysis for the target genes of the 4 validated miRNAs identified cellular senescence and neuroinflammation as key post-IS response pathways. The results of our analyses closely correlated with the pathogenesis and implicated pathways observed in IS subjects suggested by the literature, which may provide aid in the development of circulating diagnostic or therapeutic targets for IS patients.
缺血性脑卒中(IS)是脑卒中的主要类型,在过去二十年中一直是第二大致死原因。通过分析其差异表达,先前的研究表明循环 microRNAs(miRNAs)可作为 IS 的潜在诊断和治疗工具。然而,这些结果的结论尚无定论,存在争议。在这项研究中,通过综合分析和真实世界验证来评估循环 miRNAs 与 IS 之间的关联。经过手动选择和筛选,提取了 29 项研究和 112 个 miRNA,从荟萃分析的结果中获得了 12 个差异表达的 miRNA。在 20 名 IS 患者和 20 名健康对照中评估了这些 miRNA。4 个 miRNA(hsa-let-7e-5p、hsa-miR-124-3p、hsa-miR-17-5p、hsa-miR-185-5p)在 IS 患者血浆样本中的表达水平显著。对 4 个验证 miRNA 的靶基因进行通路和生物过程富集分析,确定细胞衰老和神经炎症是 IS 后关键的反应途径。我们分析的结果与文献中观察到的 IS 患者发病机制和涉及的途径密切相关,这可能有助于为 IS 患者开发循环诊断或治疗靶点。