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血浆microRNA-135a及microRNA-210在轻度认知损害患者中的检测价值

The detection of plasma microRNA-135a and microRNA-210 in the patient of mild cognitive impairment
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摘要 目的探讨血浆microRNA-135a、microRNA-210在轻度认知损害患者中的诊断价值。方法收集于我院就诊的轻度认知损害患者及健康体检者的血液标本共80例,其中AMC组28例,VD-MCI28例,AD-MCI24例,采用RT-qPCR的方法进行血浆miRNA检测。结果VD-MCI组血浆microRNA-135a为(4.17×10^-7±8.35×10^-8);AD-MCI组血浆microRNA-135a为(2.83×10^-7±1.72×10^-7);AMC组血浆microRNA-135a为(9.87×10^-7±5.66×10^-7)。3组患者组间比较存在显著差异(F=30.76,P=0.00,P<0.05)。VD-MCI组血浆microRNA-210为(4.27×10^-5±1.09×10^-5);AD-MCI组血浆microRNA-210为(6.96×10^-5±2.48×10^-5);AMC组血浆microRNA-210(1.30×10^-5±7.07×10^-6)。3组患者组间比较存在显著差异(F=80.43,P=0.00,P<0.05)。3组患者MMSE评分与两个检测指标间无明显相关性(P>0.05)。结论血浆microRNA-135a及microRNA-210检测可辅助诊断轻度认知功能损害,对AD-MCI诊断价值更大。 Objective To evaluate the clinical value of plasma microRNA-135a,microRNA-210 in the detection of mild cognitive impairment.Methods The plasma samples of 80 subjects were collected from our hospital.There were 28 people with VD-MCI,24 people with AD-MCI and 28 age-matched control(AMC).RT-qPCR was applied to test the level of microRNA-135a and microRNA-210.Results The levels of microRNA-135a in plasma were(4.17×10^-7±8.35×10^-8),(2.83×10^-7±1.72×10^-7)and(9.87×10^-7±5.66×10^-7)in VD-MCI,AD-MCI and AMC.There were difference among three groups(F=30.76,P=0.00,P<0.05).The levels of microRNA-210 in plasma were(4.27×10^-5±1.09×10^-5),(6.96×10^-5±2.48×10^-5)and(1.30×10^-5±7.07×10^-6)in VD-MCI,AD-MCI and AMC.There were difference among three groups(F=80.43,P=0.00,P<0.05).There were no correlations between the MMSE score and the two biomarkers(P>0.05).Conclusions The plasma microRNA-135a and microRNA 210 were potential biomarkers of MCI,especially for AD-MCI.
作者 胡轶虹 白春艳 李宗树 吕金珠 杨春丽 孙宏侠 HU Yihong;BAI Chunyan;LI Zongshu(Department of Neurology,Jilin Province People’s Hospital,Changchun 130021,China)
出处 《中风与神经疾病杂志》 CAS 2019年第6期527-530,共4页 Journal of Apoplexy and Nervous Diseases
基金 吉林省自然科学基金(No.20160101178JC)
关键词 轻度认知损害 微小RNA 生物标志物 Mild cognitive impairment(MCI) MicroRNA Biomarker
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  • 1Kirshner HS.Primary progressive aphasia and Alzheimer's disease:brief history,recent evidence[J].Curr Neurol Neurosci Rep,2012;12(6):709-14.
  • 2Finder VH.Alzheimer's disease:a general introduction and pathomechanism[J].J Alzheimers Dis,2010;30(Suppl 3):5-19.
  • 3Galluzzi S,Geroldi C,Amicucci G,et al.Supporting evidence for using biomarkers in the diagnosis of MCI due to AD[J].J Neurol,2013;260(2):640-50.
  • 4Liu CG,Wang JL,Li L,et al.MicroRNA-384 regulates both amyloid precursor protein andβ-secretase expression and is a potential biomarker for Alzheimer's disease[J].Int J Mol Med,2014;34(1):160-6.
  • 5Livak KJ,Schmittgen TD.Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T))method[J].Methods,2001;25(4):402-8.
  • 6Yan R,Vassar R.Targeting theβsecretase BACE1 for Alzheimer's disease therapy[J].Lancet Neurol,2014;13(3):319-29.
  • 7Vos SJ,Xiong C,Visser PJ,et al.Preclinical Alzheimer's disease and its outcome:a longitudinal cohort study[J].Lancet Neurol,2013;12(10):957-65.
  • 8Finder VH.Alzheimer's disease:a general introduction and pathomechanism[J].J Alzheimers Dis,2010;3:5-19.
  • 9Snyder HM,Carrillo MC,Grodstein F,et al.Developing novel bloodbased biomarkers for Alzheimer's disease[J].Alzheimers Dement,2014;10(1):109-14.
  • 10Kooijmans SA,Vader P,van Dommelen SM,et al.Exosome mimetics:a novel class of drug delivery systems[J].Int J Nanomedicine,2012;7:1525-41.

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