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Amyloid-beta 42 adsorption following serial tube transfer
INTRODUCTION: Cerebrospinal fluid (CSF) amyloid-beta 38 (Aβ38), 40 (Aβ40), 42 (Aβ42) and total tau (T-tau) are finding increasing utility as biomarkers of Alzheimer’s disease (AD). The purpose of this study was to determine whether measured CSF biomarker concentrations were affected by transfer of C...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4059346/ https://www.ncbi.nlm.nih.gov/pubmed/24472496 http://dx.doi.org/10.1186/alzrt236 |
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author | Toombs, Jamie Paterson, Ross W Schott, Jonathan M Zetterberg, Henrik |
author_facet | Toombs, Jamie Paterson, Ross W Schott, Jonathan M Zetterberg, Henrik |
author_sort | Toombs, Jamie |
collection | PubMed |
description | INTRODUCTION: Cerebrospinal fluid (CSF) amyloid-beta 38 (Aβ38), 40 (Aβ40), 42 (Aβ42) and total tau (T-tau) are finding increasing utility as biomarkers of Alzheimer’s disease (AD). The purpose of this study was to determine whether measured CSF biomarker concentrations were affected by transfer of CSF between tubes, and whether addition of a non-ionic surfactant mitigates any observed effects. METHODS: AD and control CSF was transferred consecutively between polypropylene tubes. Aβ peptides and T-tau were measured with and without addition of Tween 20 (0.05%). RESULTS: Measured concentrations of Aβ42 decreased by approximately 25% with each consecutive transfer. Measured concentrations of Aβ38 and Aβ40 were also observed to decrease significantly with each consecutive transfer (approximately 16% loss per transfer). Measured concentrations of T-tau also decreased significantly, but at much smaller magnitude than the Aβ peptides (approximately 4% loss per transfer). The addition of Tween 20 mitigated this effect in all samples. CONCLUSIONS: Consecutive CSF transfer between tubes has a significant impact on the measured concentration of all Aβ peptides, and significant effect of lesser magnitude on T-tau. This would be sufficient to alter biomarker ratios enough to mislead diagnosis. The introduction of Tween 20 at the initial aliquoting stage was observed to significantly mitigate this effect. |
format | Online Article Text |
id | pubmed-4059346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40593462014-06-30 Amyloid-beta 42 adsorption following serial tube transfer Toombs, Jamie Paterson, Ross W Schott, Jonathan M Zetterberg, Henrik Alzheimers Res Ther Research INTRODUCTION: Cerebrospinal fluid (CSF) amyloid-beta 38 (Aβ38), 40 (Aβ40), 42 (Aβ42) and total tau (T-tau) are finding increasing utility as biomarkers of Alzheimer’s disease (AD). The purpose of this study was to determine whether measured CSF biomarker concentrations were affected by transfer of CSF between tubes, and whether addition of a non-ionic surfactant mitigates any observed effects. METHODS: AD and control CSF was transferred consecutively between polypropylene tubes. Aβ peptides and T-tau were measured with and without addition of Tween 20 (0.05%). RESULTS: Measured concentrations of Aβ42 decreased by approximately 25% with each consecutive transfer. Measured concentrations of Aβ38 and Aβ40 were also observed to decrease significantly with each consecutive transfer (approximately 16% loss per transfer). Measured concentrations of T-tau also decreased significantly, but at much smaller magnitude than the Aβ peptides (approximately 4% loss per transfer). The addition of Tween 20 mitigated this effect in all samples. CONCLUSIONS: Consecutive CSF transfer between tubes has a significant impact on the measured concentration of all Aβ peptides, and significant effect of lesser magnitude on T-tau. This would be sufficient to alter biomarker ratios enough to mislead diagnosis. The introduction of Tween 20 at the initial aliquoting stage was observed to significantly mitigate this effect. BioMed Central 2014-01-28 /pmc/articles/PMC4059346/ /pubmed/24472496 http://dx.doi.org/10.1186/alzrt236 Text en Copyright © 2014 Toombs et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Research Toombs, Jamie Paterson, Ross W Schott, Jonathan M Zetterberg, Henrik Amyloid-beta 42 adsorption following serial tube transfer |
title | Amyloid-beta 42 adsorption following serial tube transfer |
title_full | Amyloid-beta 42 adsorption following serial tube transfer |
title_fullStr | Amyloid-beta 42 adsorption following serial tube transfer |
title_full_unstemmed | Amyloid-beta 42 adsorption following serial tube transfer |
title_short | Amyloid-beta 42 adsorption following serial tube transfer |
title_sort | amyloid-beta 42 adsorption following serial tube transfer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4059346/ https://www.ncbi.nlm.nih.gov/pubmed/24472496 http://dx.doi.org/10.1186/alzrt236 |
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