| Literature DB >> 27216941 |
Julia Kuhlmann1, Ulf Andreasson2, Josef Pannee2, Maria Bjerke2, Erik Portelius2, Andreas Leinenbach3, Tobias Bittner3, Magdalena Korecka4, Rand G Jenkins5, Hugo Vanderstichele6, Erik Stoops6, Piotr Lewczuk7, Leslie M Shaw4, Ingrid Zegers1, Heinz Schimmel1, Henrik Zetterberg8, Kaj Blennow9.
Abstract
The 42 amino acid form of amyloid β (Aβ1-42) in cerebrospinal fluid (CSF) has been widely accepted as a central biomarker for Alzheimer's disease. Several immunoassays for CSF Aβ1-42 are commercially available, but can suffer from between laboratory and batch-to-batch variability as well as lack of standardisation across assays. As a consequence, no general cut-off values have been established for a specific context of use (e.g., clinical diagnostics) and selection of individuals for enrolment in clinical trials (patient stratification) remains challenging. The International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) has initiated a working group for CSF proteins (WG-CSF) to facilitate standardisation of CSF Aβ1-42 measurement results. The efforts of the IFCC WG-CSF include the development of certified reference materials (CRMs) and reference measurement procedures (RMPs) for key biomarkers. Two candidate RMPs for quantification of Aβ1-42 in CSF based on liquid chromatography tandem mass spectrometry have been developed and tested in two ring trials. Furthermore, two commutability studies including native CSF pools, artificial CSF and spiked materials have been completed. On the basis of these studies, human CSF pools containing only endogenous Aβ1-42 at three concentrations were selected as the format for future CRMs that are now being processed.Entities:
Keywords: Alzheimer's disease; Aβ(1–42); Cerebrospinal fluid; Certified reference material; Reference measurement procedure
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Year: 2016 PMID: 27216941 DOI: 10.1016/j.cca.2016.05.014
Source DB: PubMed Journal: Clin Chim Acta ISSN: 0009-8981 Impact factor: 3.786