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Lessons from Multicenter Studies on CSF Biomarkers for Alzheimer's Disease
Several single-center studies have confirmed the usability of cerebrospinal fluid (CSF) biomarkers for the diagnosis of Alzheimer's disease (AD), even in early disease stages. Large scale multicenter studies have principally confirmed this, although such studies have also indicated the presence...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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SAGE-Hindawi Access to Research
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915803/ https://www.ncbi.nlm.nih.gov/pubmed/20721354 http://dx.doi.org/10.4061/2010/610613 |
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author | Mattsson, Niklas Zetterberg, Henrik Blennow, kaj |
author_facet | Mattsson, Niklas Zetterberg, Henrik Blennow, kaj |
author_sort | Mattsson, Niklas |
collection | PubMed |
description | Several single-center studies have confirmed the usability of cerebrospinal fluid (CSF) biomarkers for the diagnosis of Alzheimer's disease (AD), even in early disease stages. Large scale multicenter studies have principally confirmed this, although such studies have also indicated the presence of significant intercenter and interlaboratory variations in biomarker measurements. Such variations may hamper the development of biomarkers and their introduction into clinical routine practice. Recently a quality control program run by the Alzheimer's Association was started in order to harmonize procedures of laboratories world-wide. This program provides both standardized guide lines and external control CSF samples, and will allow longitudinal evaluation of laboratory performance. |
format | Text |
id | pubmed-2915803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | SAGE-Hindawi Access to Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-29158032010-08-18 Lessons from Multicenter Studies on CSF Biomarkers for Alzheimer's Disease Mattsson, Niklas Zetterberg, Henrik Blennow, kaj Int J Alzheimers Dis Review Article Several single-center studies have confirmed the usability of cerebrospinal fluid (CSF) biomarkers for the diagnosis of Alzheimer's disease (AD), even in early disease stages. Large scale multicenter studies have principally confirmed this, although such studies have also indicated the presence of significant intercenter and interlaboratory variations in biomarker measurements. Such variations may hamper the development of biomarkers and their introduction into clinical routine practice. Recently a quality control program run by the Alzheimer's Association was started in order to harmonize procedures of laboratories world-wide. This program provides both standardized guide lines and external control CSF samples, and will allow longitudinal evaluation of laboratory performance. SAGE-Hindawi Access to Research 2010-07-08 /pmc/articles/PMC2915803/ /pubmed/20721354 http://dx.doi.org/10.4061/2010/610613 Text en Copyright © 2010 Niklas Mattsson et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Mattsson, Niklas Zetterberg, Henrik Blennow, kaj Lessons from Multicenter Studies on CSF Biomarkers for Alzheimer's Disease |
title | Lessons from Multicenter Studies on CSF Biomarkers for Alzheimer's Disease |
title_full | Lessons from Multicenter Studies on CSF Biomarkers for Alzheimer's Disease |
title_fullStr | Lessons from Multicenter Studies on CSF Biomarkers for Alzheimer's Disease |
title_full_unstemmed | Lessons from Multicenter Studies on CSF Biomarkers for Alzheimer's Disease |
title_short | Lessons from Multicenter Studies on CSF Biomarkers for Alzheimer's Disease |
title_sort | lessons from multicenter studies on csf biomarkers for alzheimer's disease |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915803/ https://www.ncbi.nlm.nih.gov/pubmed/20721354 http://dx.doi.org/10.4061/2010/610613 |
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