| Literature DB >> 22917144 |
Marta del Campo1, Brit Mollenhauer, Antonio Bertolotto, Sebastiaan Engelborghs, Harald Hampel, Anja Hviid Simonsen, Elisabeth Kapaki, Niels Kruse, Nathalie Le Bastard, Sylvain Lehmann, Jose L Molinuevo, Lucilla Parnetti, Armand Perret-Liaudet, Javier Sáez-Valero, Esen Saka, Andrea Urbani, Eugeen Vanmechelen, Marcel Verbeek, Pieter Jelle Visser, Charlotte Teunissen.
Abstract
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.Entities:
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Year: 2012 PMID: 22917144 DOI: 10.2217/bmm.12.46
Source DB: PubMed Journal: Biomark Med ISSN: 1752-0363 Impact factor: 2.851