Cargando…
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...
Autores principales: | , , |
---|---|
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 |
_version_ | 1782310624292765696 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3978734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT ossenkoppelerik amyloidimaginginclinicaltrials AT prinsnielsd amyloidimaginginclinicaltrials AT vanberckelbartnm amyloidimaginginclinicaltrials |