期刊文献+

脑脊液tau蛋白预测阿尔茨海默病的Meta分析 被引量:1

Clinical value of tau protein in cerebrospinal fluid for prediction of Alzheimer′s disease: a Meta-analysis
下载PDF
导出
摘要 目的评价脑脊液(CSF)总tau蛋白(t-tau)和磷酸化tau蛋白(p-tau)浓度预测阿尔茨海默病(Alzheimer's disease,AD)的有效性和准确性。方法全面检索tau蛋白浓度预测轻度认知功能障碍(mild cognitive impairment,MCI)转化为AD的诊断性试验文献,评价纳入文献的质量,用Review Manager 5.1和Meta Disk 1.4软件进行Meta分析,计算合并效应量。结果共纳入15项研究,MCI进展为AD的t-tau基线浓度(pg/mL)高于对照组[加权均数差(WMD):320.7;95%CI:274.2~367.3],p-tau基线浓度(pg/mL)亦高于对照组(WMD:32.8;95%CI:29.5~36.0)。t-tau预测AD的诊断优势比(diagnostic odds ration,DOR)为14.1(95%CI:8.2~24.4);p-tau的DOR为22.4(95%CI:10.4~48.3)。结论 CSF中tau蛋白可作为预测AD发生的重要指标。 Objective To evaluate the efficiency and accuracy of total tau(t-tau) and phosphorylated tau(p-tau) proteins in cerebrospinal fluid(CSF) as biomarkers for predicting Alzheimer′s disease(AD).Methods The published clinical literatures which aimed to investigate the concentration of tau protein to predict the conversion of mild cognitive impairment(MCI) to AD were retrieved.The quality of all the included literatures was assessed.Meta-analysis was carried out by the software Review Manager 5.1 and Meta Disk 1.4.Results Fifteen literatures that met the inclusion criteria were included in this study.The baseline concentrations(pg/mL) of both t-tau and p-tau in MCI to AD patients were higher than those in control group.The weighted mean difference(WMD) of t-tau in MCI to AD patients was 320.7,95%CI: 274.2-367.3,and WMD of p-tau was 32.8,95%CI: 29.5-36.0).Overall diagnostic odds ratios(DOR) of t-tau and p-tau were 14.1(95%CI: 8.2-24.4) and 22.4(95%CI: 10.4-48.3) respectively.Conclusion Tau in CSF may be an important diagnostic marker for predicting AD.
出处 《临床检验杂志》 CAS CSCD 北大核心 2011年第3期182-184,共3页 Chinese Journal of Clinical Laboratory Science
基金 南通市重大科技创新专项项目(XA2009001) 南通大学医学院科研项目(2008K-9)
关键词 阿尔茨海默病 总tau蛋白 磷酸化TAU蛋白 预测 META分析 Alzheimer′s disease tau protein prediction Meta-analysis
  • 相关文献

参考文献17

  • 1Mann R, Hewitt CE, Gilbody SM. Assessing the quality of diagnos- tic studies using psychometric instruments: applying QUADAS [ J ]. Soc Psychiatry Psychiatr Epidemiol, 2009, 44 (4) :300-307.
  • 2Andreasen N, Minthon L, Vanmechelen E, et al. Cerebrospinal flu- id tau and Aβ42 as predietors of development of Alzheimer's disease in patients with mild eognitive impairment[J]. Neurosei Lett, 1999, 273 ( 1 ) : 5-8.
  • 3Maruyama M, Arai H, Sugita M, et al. Cerebrospinal fluid amyloid β (1-42) levels in the mild cognitive impairment stage of Alzheimer's disease[ J ]. Exp Neurol, 2001, 172 (2) :433-436.
  • 4Andreasen N, Vanmechelen E, Vanderstichele H, et al. Cerebrospinal fluid levels of total-tau, phospho-tau and Aβ42 predicts develop- ment of Alzheimer's disease in patients with mild cognitive impairment[J]. Acta Neurol Scand Suppt, 2003, 107(179) :47-51.
  • 5Hampel H, Teipel SJ, Fuchsberger T, et al. Value of CSF β-amy- loid1-42 and tan as predictors of Alzheimer's disease in patients with mild cognitive impairment[J]. Mol Psychiatry, 2004, 9(7):705-710.
  • 6Maruyama M, Matsui T, Tanji H, et al. Cerebrospinal fluid tau protein and periventricular white matter lesions in patients with mild cognitive impairment: implications for 2 major pathways[ J]. Arch Neu- rol, 2004, 61(5):716-520.
  • 7Herukka SK, Hallikainen M, Soininen H, et al. CSF Aβ42 and tau or phosphorylated tau and prediction of progressive mild cognitive impaimaent[ J]. Neurology, 2005, 64(7 ) : 1294-1297.
  • 8Ivanoiu A, Sindic CJ. Cerebrospinal fluid tau protein and amyloid β 42 in mild cognitive impairment: prediction of progression to Alzheimer's disease and correlation with the neuropsychological examination [J]. Neurocase, 2005, 11 ( 1 ) :32-39.
  • 9Hansson O, Zetterberg H, Buchhave P, et al. Association between CSF biomarkers and incipient Alzheimer's disease in patients with mild cognitive impairment: a follow-up study [ J]. Lancet Neurol,2006, 5(3) :228-234.
  • 10Schonknecht P, Pantel J, Kaiser E, et al. Increased tau protein differentiates mild cognitive impairment from geriatric depression and predicts conversion to dementia[J]. Neurosci Lett, 2007, 416 ( 1 ) :39-42.

同被引文献29

  • 1Miller G. Stopping Alzheimer ’ s before it starts [J]. Science,2012,337:790-792.
  • 2k,Alonso Adel C,Chen S,et ai.Tau pathd(^y in Alzheimer diseeeeand other taiiopathies [ J ]. Biochim Biophys Acta ,2005,1739 : 198-210.
  • 3Kim J, Basak JM, Holtzman DM. The role of apolipoprotein E inAlzheimer’s disease [ J]. Neuro,2009,63 : 287-303.
  • 4Bu G.Apolipoprotein E and its receptors in Alzheimer’s disease:path-ways ,pathogenesis and therapy [J]. Nat Rev Neurosci ,2009,10 :333-344.
  • 5Liu Q,Zerbinatti CY,ZhaH^; j,et al. Ariiylbid precursor protein reg-ulates bi^in apblipoprotein E and cholesterol metabolism throughlipoprotein receptor LRP1 [ J]. Neuron,2007 ,56 :66-78.
  • 6Stokin GB,Lillo C,Falzone TL, et al. The origin and transport defi-cits early in the pathogenesis of Alzheimer ’ s disease [ J ]. Science,2(X)5 ,307:1282-1288.
  • 7Xiao AW, He J, Wang Q, et al. The origin and development ofplaques and phosphorylated tau are associated with axonopathy inAlzheimer,s disease[ J]. Neurosci Bull,2011 ,27 :287-299.
  • 8Vetrivel KS/Hiinakaran G. Membrane rafts in Alzheimer’s disease be-ta-amyloid production[J]. Biochim Biophys Acta,2010,1801 :860-867.
  • 9Beel AJ,Sakakura M, Barrett PJ,et al. Direct binding of choles-terol to the amyloid precursor protein : An important interaction inlipid-Alzheimer,s disease relation ships biochim[ J]. Biophys Ac-ta,2010,1801 :975-982.
  • 10Reid PC,Urano Y,Kodama T,et al. Alzheimer’s disease:choles-terol,membrane rafts,isoprenoids and statins [ J ]. J Cell Med,2007,11 :383-392.

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部