| Literature DB >> 33788410 |
Oskar Hansson1,2, Richard Batrla3, Britta Brix4, Maria C Carrillo5, Veronika Corradini6, Rebecca M Edelmayer5, Rianne N Esquivel7, Christina Hall8, John Lawson7, Nathalie Le Bastard9, José Luis Molinuevo10,11, Laura K Nisenbaum12, Sandra Rutz13, Salvatore J Salamone14, Charlotte E Teunissen15, Christopher Traynham7, Robert M Umek16, Hugo Vanderstichele17, Manu Vandijck9, Simone Wahl14, Christopher J Weber5, Henrik Zetterberg18,19,20,21, Kaj Blennow18,19.
Abstract
The core cerebrospinal fluid (CSF) Alzheimer's disease (AD) biomarkers amyloid beta (Aβ42 and Aβ40), total tau, and phosphorylated tau, have been extensively clinically validated, with very high diagnostic performance for AD, including the early phases of the disease. However, between-center differences in pre-analytical procedures may contribute to variability in measurements across laboratories. To resolve this issue, a workgroup was led by the Alzheimer's Association with experts from both academia and industry. The aim of the group was to develop a simplified and standardized pre-analytical protocol for CSF collection and handling before analysis for routine clinical use, and ultimately to ensure high diagnostic performance and minimize patient misclassification rates. Widespread application of the protocol would help minimize variability in measurements, which would facilitate the implementation of unified cut-off levels across laboratories, and foster the use of CSF biomarkers in AD diagnostics for the benefit of the patients.Entities:
Keywords: Alzheimer's disease; Amyloid Beta; Biomarkers; CSF; Cerebrospinal Fluid; Diagnosis; Fresh CSF; Frozen CSF; Handling; Measurements; Pre-Analytical; Tau
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Year: 2021 PMID: 33788410 DOI: 10.1002/alz.12316
Source DB: PubMed Journal: Alzheimers Dement ISSN: 1552-5260 Impact factor: 21.566