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首页> 外文期刊>Clinica chimica acta: International journal of clinical chemistry and applied molecular biology >Pre-analytical and analytical factors influencing Alzheimer's disease cerebrospinal fluid biomarker variability
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Pre-analytical and analytical factors influencing Alzheimer's disease cerebrospinal fluid biomarker variability

机译:影响阿尔茨海默氏病脑脊液生物标志物变异的分析前和分析因素

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A panel of cerebrospinal fluid (CSF) biomarkers including total Tau (t-Tau), phosphorylated Tau protein at residue 181 (p-Tau) and beta-amyloid peptides (A beta(42) and A beta(40)), is frequently used as an aid in Alzheimer's disease (AD) diagnosis for young patients with cognitive impairment, for predicting prodromal AD in mild cognitive impairment (MCI) subjects, for AD discrimination in atypical clinical phenotypes and for inclusion/exclusion and stratification of patients in clinical trials. Due to variability in absolute levels between laboratories, there is no consensus on medical cut-off value for the CSF AD signature. Thus, for full implementation of this core AD biomarker panel in clinical routine, this issue has to be solved. Variability can be explained both by pre-analytical and analytical factors. For example, the plastic tubes used for CSF collection and storage, the lack of reference material and the variability of the analytical protocols were identified as important sources of variability. The aim of this review is to highlight these pre-analytical and analytical factors and describe efforts done to counteract them in order to establish cut-off values for core CSF AD biomarkers. This review will give the current state of recommendations. (C) 2015 Published by Elsevier B.V.
机译:经常会出现一组脑脊液(CSF)生物标志物,包括总Tau(t-Tau),残基181处的磷酸化Tau蛋白(p-Tau)和β-淀粉样肽(A beta(42)和A beta(40))。用作辅助性认知障碍年轻患者的阿尔茨海默氏病(AD)诊断,预测轻度认知障碍(MCI)受试者的前驱性AD,用于非典型临床表型的AD歧视以及用于临床试验中患者的纳入/排除和分层。由于实验室之间的绝对水平存在差异,因此对于CSF AD签名的医学临界值尚无共识。因此,为了在临床常规中完全实施该核心AD生物标志物组,必须解决该问题。可变性可以通过分析前因素和分析因素来解释。例如,用于CSF收集和储存的塑料管,缺少参考材料以及分析规程的可变性被确定为可变性的重要来源。这篇综述的目的是突出这些分析前和分析因素,并描述为抵消它们而做出的努力,以便确定核心CSF AD生物标志物的临界值。这次审查将提供建议的当前状态。 (C)2015由Elsevier B.V.发布

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