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PET Imaging in Preclinical Anti-Aβ Drug Development

Positron emission tomography (PET), a medical imaging technique allowing for studies of the living human brain, has gained an important role in clinical trials of novel drugs against Alzheimer’s disease (AD). For example, PET data contributed to the conditional approval in 2021 of aducanumab, an ant...

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Autores principales: Syvänen, Stina, Meier, Silvio R., Roshanbin, Sahar, Xiong, Mengfei, Faresjö, Rebecca, Gustavsson, Tobias, Bonvicini, Gillian, Schlein, Eva, Aguilar, Ximena, Julku, Ulrika, Eriksson, Jonas, Sehlin, Dag
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9246809/
https://www.ncbi.nlm.nih.gov/pubmed/35501533
http://dx.doi.org/10.1007/s11095-022-03277-z
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author Syvänen, Stina
Meier, Silvio R.
Roshanbin, Sahar
Xiong, Mengfei
Faresjö, Rebecca
Gustavsson, Tobias
Bonvicini, Gillian
Schlein, Eva
Aguilar, Ximena
Julku, Ulrika
Eriksson, Jonas
Sehlin, Dag
author_facet Syvänen, Stina
Meier, Silvio R.
Roshanbin, Sahar
Xiong, Mengfei
Faresjö, Rebecca
Gustavsson, Tobias
Bonvicini, Gillian
Schlein, Eva
Aguilar, Ximena
Julku, Ulrika
Eriksson, Jonas
Sehlin, Dag
author_sort Syvänen, Stina
collection PubMed
description Positron emission tomography (PET), a medical imaging technique allowing for studies of the living human brain, has gained an important role in clinical trials of novel drugs against Alzheimer’s disease (AD). For example, PET data contributed to the conditional approval in 2021 of aducanumab, an antibody directed towards amyloid-beta (Aβ) aggregates, by showing a dose-dependent reduction in brain amyloid after treatment. In parallel to clinical studies, preclinical studies in animal models of Aβ pathology may also benefit from PET as a tool to detect target engagement and treatment effects of anti-Aβ drug candidates. PET is associated with a high level of translatability between species as similar, non-invasive protocols allow for longitudinal rather than cross-sectional studies and can be used both in a preclinical and clinical setting. This review focuses on the use of preclinical PET imaging in genetically modified animals that express human Aβ, and its present and potential future role in the development of drugs aimed at reducing brain Aβ levels as a therapeutic strategy to halt disease progression in AD.
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spelling pubmed-92468092022-07-02 PET Imaging in Preclinical Anti-Aβ Drug Development Syvänen, Stina Meier, Silvio R. Roshanbin, Sahar Xiong, Mengfei Faresjö, Rebecca Gustavsson, Tobias Bonvicini, Gillian Schlein, Eva Aguilar, Ximena Julku, Ulrika Eriksson, Jonas Sehlin, Dag Pharm Res Expert Review Positron emission tomography (PET), a medical imaging technique allowing for studies of the living human brain, has gained an important role in clinical trials of novel drugs against Alzheimer’s disease (AD). For example, PET data contributed to the conditional approval in 2021 of aducanumab, an antibody directed towards amyloid-beta (Aβ) aggregates, by showing a dose-dependent reduction in brain amyloid after treatment. In parallel to clinical studies, preclinical studies in animal models of Aβ pathology may also benefit from PET as a tool to detect target engagement and treatment effects of anti-Aβ drug candidates. PET is associated with a high level of translatability between species as similar, non-invasive protocols allow for longitudinal rather than cross-sectional studies and can be used both in a preclinical and clinical setting. This review focuses on the use of preclinical PET imaging in genetically modified animals that express human Aβ, and its present and potential future role in the development of drugs aimed at reducing brain Aβ levels as a therapeutic strategy to halt disease progression in AD. Springer US 2022-05-02 2022 /pmc/articles/PMC9246809/ /pubmed/35501533 http://dx.doi.org/10.1007/s11095-022-03277-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Expert Review
Syvänen, Stina
Meier, Silvio R.
Roshanbin, Sahar
Xiong, Mengfei
Faresjö, Rebecca
Gustavsson, Tobias
Bonvicini, Gillian
Schlein, Eva
Aguilar, Ximena
Julku, Ulrika
Eriksson, Jonas
Sehlin, Dag
PET Imaging in Preclinical Anti-Aβ Drug Development
title PET Imaging in Preclinical Anti-Aβ Drug Development
title_full PET Imaging in Preclinical Anti-Aβ Drug Development
title_fullStr PET Imaging in Preclinical Anti-Aβ Drug Development
title_full_unstemmed PET Imaging in Preclinical Anti-Aβ Drug Development
title_short PET Imaging in Preclinical Anti-Aβ Drug Development
title_sort pet imaging in preclinical anti-aβ drug development
topic Expert Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9246809/
https://www.ncbi.nlm.nih.gov/pubmed/35501533
http://dx.doi.org/10.1007/s11095-022-03277-z
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