在缺血性中风患者中,血清miR-142-5p升高与缺血性病变以及NSE和S100β相关
WeiWei Xu1, YongXia Cheng2, Ning An3
1Department of Neurology 3, Hongqi Hospital Affiliated to Mudanjiang Medical College, Mudanjiang, Heilongjiang, 157011, China.
Open medicine (Warsaw, Poland)
|December 13, 2024
概括
在缺血性中风 (IS) 患者中,MicroRNA-142-5p,神经元特异性酶 (NSE) 和S100β的水平升高. 较高的水平与中风的严重程度相关,并且随着治疗而改善,表明作为生物标志物的潜力.
科学领域:
- 生物化学 生物化学
- 分子生物学分子生物学
- 神经学 神经学
背景情况:
- 缺血性中风 (IS) 是一个重大的健康挑战.
- 确定可靠的生物标志物用于IS诊断和预后至关重要.
- 微RNAs (miRNAs) 正在成为潜在的诊断和预后指标.
研究的目的:
- 在IS患者中调查特定miRNA与已确定的神经损伤标志物之间的相关性.
- 评估这些标志物的潜力,以评估IS的严重程度和治疗反应.
主要方法:
- 追溯分析86名IS患者和32名健康对照.
- 使用RT-qPCR和ELISA测量血清中的miR-142-5p,神经元特异性酶 (NSE) 和S100β.
- 使用国家卫生研究院中风量表 (NIHSS) 评估神经系统缺陷.
主要成果:
- 与对照组相比,IS患者的血清miR-142-5p,NSE和S100β显著升高.
- 这些标志物的血清水平在治疗2周后下降,并且在康复较好的患者中较低.
- miR-142-5p与NSE,S100β和NIHSS分数呈现出正相关性.
结论:
- 在IS患者中血清miR-142-5p,NSE和S100β的水平升高.
- 这些标记物相互积极相关,并且与中风的严重程度有关.
- miR-142-5p显示为在缺血性中风管理中的潜在生物标志物具有前途.
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