期刊文献+

老年性痴呆血浆中Aβ1-42、Aβ1-40及p-tau(^(181)P)蛋白的临床诊断意义 被引量:13

Study of Plasma Levels of Aβ1-42,Aβ1-40 and p-tau(^(181)P) in Alzheimer Disease
下载PDF
导出
摘要 目的探讨血浆中β淀粉样蛋白(Aβ)142、Aβ140及过度磷酸化微管相关蛋白p tau(181P)对老年性痴呆(AD)的诊断意义。方法采用分层法选择早期AD患者23例(19≤MMSE≤26,CDR=1),中后期AD患者35例(MMSE<19,CDR≥2)及年龄、性别相匹配的健康对照组(HC)30例。所采集血标本置EDTA抗凝管中,低温离心取上清,加酸置低温冰箱保存。应用ELISA方法检测血浆Aβ142、Aβ140及p tau(181P)蛋白水平。结果早期AD患者血浆Aβ142浓度较HC组显著升高,随着病情加重AD患者血浆Aβ142浓度明显下降,至中后期其水平与HC组差异无显著性。而AD各组患者血浆Aβ140浓度与HC组比较差异无显著性。AD患者血浆中可检测到p tau(181P)蛋白且特异性较高,中后期AD患者血浆p tau(181P)蛋白浓度较HC组显著升高。结论根据病程将AD患者进行分层并对血标本进行特殊处理,检测血浆中Aβ142、Aβ140及p tau(181P)蛋白浓度可能成为临床辅助诊断AD的生物指标。 Objective To study the early diagnostic significance of improved method for determining plasma level of Aβ1-42, Aβ1-40 and p-tau (^(181)P) in Alzheimer disease. Methods Subjects with 23mild AD (19≤MMSE≤26) and 35 moderate and severe AD(MMSE<19, CDR≥2) and age-matched healthy control (HC, n=30) were included in this study. Improved sample collection and ELISA method were adopted. Results The sensitivity of improved eetermination method was significantly increased. The levels of Aβ1-42 in mild AD group was significantly statistically (P<0.001) higher than that in HC, and level of Aβ1-42 was similar between patients in the moderate-group and HC. The plasma Aβ1-40 in total AD group was slightly but not statistically significntly higher than that in HC group. Level of p-tau(^(181)P) was statistically significantly higher (P<0.001) in the severe AD group than that in HC.Conclusions The improved method for determining plasma Aβ1-42, Aβ1-40 and p-tau(^(181)P) might be a useful biochemical tool for the diagnosis of AD.
出处 《中国神经免疫学和神经病学杂志》 CAS 2005年第4期208-211,共4页 Chinese Journal of Neuroimmunology and Neurology
关键词 老年性痴呆 p-tau(^181p)蛋白 AΒ1-42 AΒ1-40 Alzheimer disease p-tau(^(181)p) protein Aβ1-42 Aβ1-40
  • 相关文献

参考文献9

  • 1Etsuro M, Mikio S, Koji A, et al. Vascular amyloidosis in neurodegenerative condition[J]. Drugs News Perspect, 2002,15:439-444.
  • 2Kuo YM, Emmerling MR, Lapert HC, et al. High levels of circulating A beta42 are sequestered by plasma proteins in AD[J].Biochem Biophys Res Commun, 1999,257: 787-794.
  • 3刘世杰 王建枝.Tau蛋白的结构、功能和异常修饰与阿尔茨海默病的关系[M].见:盛树力.老年性痴呆:发病机理与药物研究[M].北京:科学技术文献出版社,2003.107-119.
  • 4Gong CX, Lidsky T, Wegiel J, et al. Phosphorylation of microtubule-associated protein tau is regulated by protein phosphatase 2A in mammalian brain implications for neurofibrillary degeneration in Alzheimer's disease[J]. J Biochem, 2000,275(8): 5535-5544.
  • 5Thurston VC, Zinkowski RP, Binder LI. Tau as a nucleolar protein in human nonneural cell in vitro and in vivo[J]. Chromosoma, 1996,105:20-30.
  • 6Martin I, Mari B, Eirikur B, et al. Tau immunoreactivity detected in human plasma, but no obvious increase in dementia[J]. Dement Geriatr Cogn Disord, 1999,10:442-445.
  • 7Hampel H, Goernitz A, Buerger K. Advances in the development of biomarkers for Alzheimer disease: from CSF total tau and Aβ1-42 ptroteins to phosphorylated tau protein[J]. Brain Res Bull, 2003,61(3): 243-253.
  • 8Hampel H, Buerger K, Zinkowski R, et al. Measurement of phosphorylated tau epitopes differential diagnosis of Alzheimer disease comparative cerebrospinal fluid study[J], Arch Gen Psychiatry, 2004,61(1): 95-102.
  • 9Andreasen N, Sjogren M, Blennow K. CSF marker for Alzheimer disease: total tau, phospho-tau and Aβ42[J]. World J Biol Psychiatry, 2003,4(4): 147-155.

同被引文献172

引证文献13

二级引证文献45

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