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Blood protein predictors of brain amyloid for enrichment in clinical trials?
BACKGROUND: Measures of neocortical amyloid burden (NAB) identify individuals who are at substantially greater risk of developing Alzheimer's disease (AD). Blood-based biomarkers predicting NAB would have great utility for the enrichment of AD clinical trials, including large-scale prevention t...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876903/ https://www.ncbi.nlm.nih.gov/pubmed/27239491 http://dx.doi.org/10.1016/j.dadm.2014.11.005 |
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author | Ashton, Nicholas J. Kiddle, Steven J. Graf, John Ward, Malcolm Baird, Alison L. Hye, Abdul Westwood, Sarah Wong, Karyuan Vivian Dobson, Richard J. Rabinovici, Gil D. Miller, Bruce L. Rosen, Howard J. Torres, Andrew Zhang, Zhanpan Thurfjell, Lennart Covin, Antonia Hehir, Cristina Tan Baker, David Bazenet, Chantal Lovestone, Simon |
author_facet | Ashton, Nicholas J. Kiddle, Steven J. Graf, John Ward, Malcolm Baird, Alison L. Hye, Abdul Westwood, Sarah Wong, Karyuan Vivian Dobson, Richard J. Rabinovici, Gil D. Miller, Bruce L. Rosen, Howard J. Torres, Andrew Zhang, Zhanpan Thurfjell, Lennart Covin, Antonia Hehir, Cristina Tan Baker, David Bazenet, Chantal Lovestone, Simon |
author_sort | Ashton, Nicholas J. |
collection | PubMed |
description | BACKGROUND: Measures of neocortical amyloid burden (NAB) identify individuals who are at substantially greater risk of developing Alzheimer's disease (AD). Blood-based biomarkers predicting NAB would have great utility for the enrichment of AD clinical trials, including large-scale prevention trials. METHODS: Nontargeted proteomic discovery was applied to 78 subjects from the Australian Imaging, Biomarkers and Lifestyle Flagship Study of Ageing with a range of NAB values. Technical and independent replications were performed by immunoassay. RESULTS: Seventeen discovery candidates were selected for technical replication. α2-Macroglobulin, fibrinogen γ-chain (FGG), and complement factor H-related protein 1 were confirmed to be associated with NAB. In an independent cohort, FGG plasma levels combined with age predicted NAB had a sensitivity of 59% and specificity of 78%. CONCLUSION: A single blood protein, FGG, combined with age, was shown to relate to NAB and therefore could have potential for enrichment of clinical trial populations. |
format | Online Article Text |
id | pubmed-4876903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-48769032016-05-27 Blood protein predictors of brain amyloid for enrichment in clinical trials? Ashton, Nicholas J. Kiddle, Steven J. Graf, John Ward, Malcolm Baird, Alison L. Hye, Abdul Westwood, Sarah Wong, Karyuan Vivian Dobson, Richard J. Rabinovici, Gil D. Miller, Bruce L. Rosen, Howard J. Torres, Andrew Zhang, Zhanpan Thurfjell, Lennart Covin, Antonia Hehir, Cristina Tan Baker, David Bazenet, Chantal Lovestone, Simon Alzheimers Dement (Amst) Blood-Based Biomarker BACKGROUND: Measures of neocortical amyloid burden (NAB) identify individuals who are at substantially greater risk of developing Alzheimer's disease (AD). Blood-based biomarkers predicting NAB would have great utility for the enrichment of AD clinical trials, including large-scale prevention trials. METHODS: Nontargeted proteomic discovery was applied to 78 subjects from the Australian Imaging, Biomarkers and Lifestyle Flagship Study of Ageing with a range of NAB values. Technical and independent replications were performed by immunoassay. RESULTS: Seventeen discovery candidates were selected for technical replication. α2-Macroglobulin, fibrinogen γ-chain (FGG), and complement factor H-related protein 1 were confirmed to be associated with NAB. In an independent cohort, FGG plasma levels combined with age predicted NAB had a sensitivity of 59% and specificity of 78%. CONCLUSION: A single blood protein, FGG, combined with age, was shown to relate to NAB and therefore could have potential for enrichment of clinical trial populations. Elsevier 2015-03-29 /pmc/articles/PMC4876903/ /pubmed/27239491 http://dx.doi.org/10.1016/j.dadm.2014.11.005 Text en © 2015 The Alzheimer’s Association. Published by Elsevier Inc. 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 Biomarker Ashton, Nicholas J. Kiddle, Steven J. Graf, John Ward, Malcolm Baird, Alison L. Hye, Abdul Westwood, Sarah Wong, Karyuan Vivian Dobson, Richard J. Rabinovici, Gil D. Miller, Bruce L. Rosen, Howard J. Torres, Andrew Zhang, Zhanpan Thurfjell, Lennart Covin, Antonia Hehir, Cristina Tan Baker, David Bazenet, Chantal Lovestone, Simon Blood protein predictors of brain amyloid for enrichment in clinical trials? |
title | Blood protein predictors of brain amyloid for enrichment in clinical trials? |
title_full | Blood protein predictors of brain amyloid for enrichment in clinical trials? |
title_fullStr | Blood protein predictors of brain amyloid for enrichment in clinical trials? |
title_full_unstemmed | Blood protein predictors of brain amyloid for enrichment in clinical trials? |
title_short | Blood protein predictors of brain amyloid for enrichment in clinical trials? |
title_sort | blood protein predictors of brain amyloid for enrichment in clinical trials? |
topic | Blood-Based Biomarker |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876903/ https://www.ncbi.nlm.nih.gov/pubmed/27239491 http://dx.doi.org/10.1016/j.dadm.2014.11.005 |
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