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Plasma amyloid β 42/40 ratios as biomarkers for amyloid β cerebral deposition in cognitively normal individuals
INTRODUCTION: Plasma amyloid β (Aβ) peptides have been previously studied as candidate biomarkers to increase recruitment efficiency in secondary prevention clinical trials for Alzheimer's disease. METHODS: Free and total Aβ42/40 plasma ratios (FP42/40 and TP42/40, respectively) were determined...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602863/ https://www.ncbi.nlm.nih.gov/pubmed/28948206 http://dx.doi.org/10.1016/j.dadm.2017.07.004 |
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author | Fandos, Noelia Pérez-Grijalba, Virginia Pesini, Pedro Olmos, Salvador Bossa, Matías Villemagne, Victor L. Doecke, James Fowler, Christopher Masters, Colin L. Sarasa, Manuel |
author_facet | Fandos, Noelia Pérez-Grijalba, Virginia Pesini, Pedro Olmos, Salvador Bossa, Matías Villemagne, Victor L. Doecke, James Fowler, Christopher Masters, Colin L. Sarasa, Manuel |
author_sort | Fandos, Noelia |
collection | PubMed |
description | INTRODUCTION: Plasma amyloid β (Aβ) peptides have been previously studied as candidate biomarkers to increase recruitment efficiency in secondary prevention clinical trials for Alzheimer's disease. METHODS: Free and total Aβ42/40 plasma ratios (FP42/40 and TP42/40, respectively) were determined using ABtest assays in cognitively normal subjects from the Australian Imaging, Biomarker and Lifestyle Flagship Study. This population was followed-up for 72 months and their cortical Aβ burden was assessed with positron emission tomography. RESULTS: Cross-sectional and longitudinal analyses showed an inverse association of Aβ42/40 plasma ratios and cortical Aβ burden. Optimized as a screening tool, TP42/40 reached 81% positive predictive value of high cortical Aβ burden, which represents 110% increase over the population prevalence of cortical Aβ positivity. DISCUSSION: These findings support the use of plasma Aβ42/40 ratios as surrogate biomarkers of cortical Aβ deposition and enrichment tools, reducing the number of subjects submitted to invasive tests and, consequently, recruitment costs in clinical trials targeting cognitively normal individuals. |
format | Online Article Text |
id | pubmed-5602863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-56028632017-09-25 Plasma amyloid β 42/40 ratios as biomarkers for amyloid β cerebral deposition in cognitively normal individuals Fandos, Noelia Pérez-Grijalba, Virginia Pesini, Pedro Olmos, Salvador Bossa, Matías Villemagne, Victor L. Doecke, James Fowler, Christopher Masters, Colin L. Sarasa, Manuel Alzheimers Dement (Amst) Blood-Based Biomarkers INTRODUCTION: Plasma amyloid β (Aβ) peptides have been previously studied as candidate biomarkers to increase recruitment efficiency in secondary prevention clinical trials for Alzheimer's disease. METHODS: Free and total Aβ42/40 plasma ratios (FP42/40 and TP42/40, respectively) were determined using ABtest assays in cognitively normal subjects from the Australian Imaging, Biomarker and Lifestyle Flagship Study. This population was followed-up for 72 months and their cortical Aβ burden was assessed with positron emission tomography. RESULTS: Cross-sectional and longitudinal analyses showed an inverse association of Aβ42/40 plasma ratios and cortical Aβ burden. Optimized as a screening tool, TP42/40 reached 81% positive predictive value of high cortical Aβ burden, which represents 110% increase over the population prevalence of cortical Aβ positivity. DISCUSSION: These findings support the use of plasma Aβ42/40 ratios as surrogate biomarkers of cortical Aβ deposition and enrichment tools, reducing the number of subjects submitted to invasive tests and, consequently, recruitment costs in clinical trials targeting cognitively normal individuals. Elsevier 2017-08-30 /pmc/articles/PMC5602863/ /pubmed/28948206 http://dx.doi.org/10.1016/j.dadm.2017.07.004 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Blood-Based Biomarkers Fandos, Noelia Pérez-Grijalba, Virginia Pesini, Pedro Olmos, Salvador Bossa, Matías Villemagne, Victor L. Doecke, James Fowler, Christopher Masters, Colin L. Sarasa, Manuel Plasma amyloid β 42/40 ratios as biomarkers for amyloid β cerebral deposition in cognitively normal individuals |
title | Plasma amyloid β 42/40 ratios as biomarkers for amyloid β cerebral deposition in cognitively normal individuals |
title_full | Plasma amyloid β 42/40 ratios as biomarkers for amyloid β cerebral deposition in cognitively normal individuals |
title_fullStr | Plasma amyloid β 42/40 ratios as biomarkers for amyloid β cerebral deposition in cognitively normal individuals |
title_full_unstemmed | Plasma amyloid β 42/40 ratios as biomarkers for amyloid β cerebral deposition in cognitively normal individuals |
title_short | Plasma amyloid β 42/40 ratios as biomarkers for amyloid β cerebral deposition in cognitively normal individuals |
title_sort | plasma amyloid β 42/40 ratios as biomarkers for amyloid β cerebral deposition in cognitively normal individuals |
topic | Blood-Based Biomarkers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602863/ https://www.ncbi.nlm.nih.gov/pubmed/28948206 http://dx.doi.org/10.1016/j.dadm.2017.07.004 |
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