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Amyloid imaging in clinical trials

The possibility to map amyloid-beta, the Alzheimer’s disease hallmark protein, in vivo opens the application for amyloid imaging in clinical trials with disease-modifying agents. Monitoring change in amyloid burden, particularly when potential amyloid-lowering drugs are at play, requires accurate an...

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Detalles Bibliográficos
Autores principales: Ossenkoppele, Rik, Prins, Niels D, van Berckel, Bart NM
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978734/
https://www.ncbi.nlm.nih.gov/pubmed/23953396
http://dx.doi.org/10.1186/alzrt195
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author Ossenkoppele, Rik
Prins, Niels D
van Berckel, Bart NM
author_facet Ossenkoppele, Rik
Prins, Niels D
van Berckel, Bart NM
author_sort Ossenkoppele, Rik
collection PubMed
description The possibility to map amyloid-beta, the Alzheimer’s disease hallmark protein, in vivo opens the application for amyloid imaging in clinical trials with disease-modifying agents. Monitoring change in amyloid burden, particularly when potential amyloid-lowering drugs are at play, requires accurate analytical methods. Studies to date have used suboptimal methods that do not account for heterogeneous changes in flow associated with disease progression and potentially with anti-amyloid drugs. In this commentary, we discuss practical and methodological issues regarding longitudinal amyloid imaging and propose several quantitative, yet feasible, alternatives for reliable assessment of changes over time in amyloid burden.
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spelling pubmed-39787342014-04-09 Amyloid imaging in clinical trials Ossenkoppele, Rik Prins, Niels D van Berckel, Bart NM Alzheimers Res Ther Commentary The possibility to map amyloid-beta, the Alzheimer’s disease hallmark protein, in vivo opens the application for amyloid imaging in clinical trials with disease-modifying agents. Monitoring change in amyloid burden, particularly when potential amyloid-lowering drugs are at play, requires accurate analytical methods. Studies to date have used suboptimal methods that do not account for heterogeneous changes in flow associated with disease progression and potentially with anti-amyloid drugs. In this commentary, we discuss practical and methodological issues regarding longitudinal amyloid imaging and propose several quantitative, yet feasible, alternatives for reliable assessment of changes over time in amyloid burden. BioMed Central 2013-08-14 /pmc/articles/PMC3978734/ /pubmed/23953396 http://dx.doi.org/10.1186/alzrt195 Text en Copyright © 2013 BioMed Central Ltd.
spellingShingle Commentary
Ossenkoppele, Rik
Prins, Niels D
van Berckel, Bart NM
Amyloid imaging in clinical trials
title Amyloid imaging in clinical trials
title_full Amyloid imaging in clinical trials
title_fullStr Amyloid imaging in clinical trials
title_full_unstemmed Amyloid imaging in clinical trials
title_short Amyloid imaging in clinical trials
title_sort amyloid imaging in clinical trials
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978734/
https://www.ncbi.nlm.nih.gov/pubmed/23953396
http://dx.doi.org/10.1186/alzrt195
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