Department of Clinical Chemistry, Neurology Laboratory, VU University medical center, De Boelelaan 1117, Amsterdam, The Netherlands.
Biomark Med. 2012 Aug;6(4):419-30. doi: 10.2217/bmm.12.46.
Early diagnosis of neurodegenerative disorders such as Alzheimer's (AD) or Parkinson's disease (PD) is needed to slow down or halt the disease at the earliest stage. Cerebrospinal fluid (CSF) biomarkers can be a good tool for early diagnosis. However, their use in clinical practice is challenging due to the high variability found between centers in the concentrations of both AD CSF biomarkers (Aβ42, total tau and phosphorylated tau) and PD CSF biomarker (α-synuclein). Such a variability has been partially attributed to different preanalytical procedures between laboratories, thus highlighting the need to establish standardized operating procedures. Here, we merge two previous consensus guidelines for preanalytical confounding factors in order to achieve one exhaustive guideline updated with new evidence for Aβ42, total tau and phosphorylated tau, and α-synuclein. The proposed standardized operating procedures are applicable not only to novel CSF biomarkers in AD and PD, but also to biomarkers for other neurodegenerative disorders.
早期诊断神经退行性疾病,如阿尔茨海默病(AD)或帕金森病(PD),需要在最早阶段减缓或阻止疾病进展。脑脊液(CSF)生物标志物可作为早期诊断的良好工具。然而,由于在 AD 脑脊液生物标志物(Aβ42、总 tau 和磷酸化 tau)和 PD 脑脊液生物标志物(α-突触核蛋白)的浓度方面,不同中心之间存在高度变异性,其在临床实践中的应用具有挑战性。这种变异性部分归因于实验室之间的不同预分析程序,因此强调需要建立标准化操作程序。在这里,我们合并了以前关于 AD 和 PD 中预分析混杂因素的两个共识指南,以获得一个更新的详尽指南,其中包含了针对 Aβ42、总 tau 和磷酸化 tau 以及 α-突触核蛋白的新证据。所提出的标准化操作程序不仅适用于 AD 和 PD 中的新型 CSF 生物标志物,也适用于其他神经退行性疾病的生物标志物。