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联合血浆生物标志物用于诊断轻度认知障碍和阿尔茨海默病。

Combined plasma biomarkers for diagnosing mild cognition impairment and Alzheimer's disease.

机构信息

Department of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University , Taipei 100, Taiwan.

出版信息

ACS Chem Neurosci. 2013 Dec 18;4(12):1530-6. doi: 10.1021/cn400129p. Epub 2013 Oct 23.

Abstract

A highly sensitive immunoassay, the immunomagnetic reduction, is used to measure several biomarkers for plasma that is related to Alzheimer's disease (AD). These biomarkers include Aβ-40, Aβ-42, and tau proteins. The samples are composed of four groups: healthy controls (n=66), mild cognitive impairment (MCI, n=22), very mild dementia (n=23), and mild-to-serve dementia, all due to AD (n=22). It is found that the concentrations of both Aβ-42 and tau protein for the healthy controls are significantly lower than those of all of the other groups. The sensitivity and the specificity of plasma Aβ-42 and tau protein in differentiating MCI from AD are all around 0.9 (0.88-0.97). However, neither plasma Aβ-42 nor tau-protein concentration is an adequate parameter to distinguish MCI from AD. A parameter is proposed, which is the product of plasma Aβ-42 and tau-protein levels, to differentiate MCI from AD. The sensitivity and specificity are found to be 0.80 and 0.82, respectively. It is concluded that the use of combined plasma biomarkers not only allows the differentiation of the healthy controls and patients with AD in both the prodromal phase and the dementia phase, but it also allows AD in the prodromal phase to be distinguished from that in the dementia phase.

摘要

一种高灵敏度的免疫分析方法,即免疫磁还原法,用于测量与阿尔茨海默病(AD)相关的几种血浆生物标志物。这些生物标志物包括 Aβ-40、Aβ-42 和 tau 蛋白。样本由四组组成:健康对照组(n=66)、轻度认知障碍(MCI,n=22)、极轻度痴呆(n=23)和轻度至重度痴呆,均归因于 AD(n=22)。结果发现,健康对照组的 Aβ-42 和 tau 蛋白浓度明显低于其他所有组。血浆 Aβ-42 和 tau 蛋白区分 MCI 与 AD 的灵敏度和特异性均约为 0.9(0.88-0.97)。然而,血浆 Aβ-42 或 tau 蛋白浓度都不是区分 MCI 与 AD 的充分参数。提出了一个参数,即血浆 Aβ-42 和 tau 蛋白水平的乘积,用于区分 MCI 与 AD。发现灵敏度和特异性分别为 0.80 和 0.82。结论是,联合使用血浆生物标志物不仅可以区分前驱期和痴呆期的健康对照者和 AD 患者,还可以区分前驱期 AD 与痴呆期 AD。

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