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APOE-amyloid interaction: Therapeutic targets

Alzheimer’s disease (AD) is a devastating neurodegenerative disorder that is growing in prevalence globally. It is the only major cause of death without any effective pharmacological means to treat or slow progression. Inheritance of the ε4 allele of the Apolipoprotein (APO) E gene is the strongest...

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Autores principales: Wisniewski, Thomas, Drummond, Eleanor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118587/
https://www.ncbi.nlm.nih.gov/pubmed/32027932
http://dx.doi.org/10.1016/j.nbd.2020.104784
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author Wisniewski, Thomas
Drummond, Eleanor
author_facet Wisniewski, Thomas
Drummond, Eleanor
author_sort Wisniewski, Thomas
collection PubMed
description Alzheimer’s disease (AD) is a devastating neurodegenerative disorder that is growing in prevalence globally. It is the only major cause of death without any effective pharmacological means to treat or slow progression. Inheritance of the ε4 allele of the Apolipoprotein (APO) E gene is the strongest genetic risk factor for late-onset AD. The interaction between APOE and amyloid β (Aβ) plays a key role in AD pathogenesis. The APOE-Aβ interaction regulates Aβ aggregation and clearance and therefore directly influences the development of amyloid plaques, congophilic amyloid angiopathy and subsequent tau related pathology. Relatively few AD therapeutic approaches have directly targeted the APOE-Aβ interaction thus far. Here we review the critical role of APOE in the pathogenesis of AD and some of the most promising therapeutic approaches that focus on the APOE-Aβ interaction.
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spelling pubmed-71185872021-05-01 APOE-amyloid interaction: Therapeutic targets Wisniewski, Thomas Drummond, Eleanor Neurobiol Dis Article Alzheimer’s disease (AD) is a devastating neurodegenerative disorder that is growing in prevalence globally. It is the only major cause of death without any effective pharmacological means to treat or slow progression. Inheritance of the ε4 allele of the Apolipoprotein (APO) E gene is the strongest genetic risk factor for late-onset AD. The interaction between APOE and amyloid β (Aβ) plays a key role in AD pathogenesis. The APOE-Aβ interaction regulates Aβ aggregation and clearance and therefore directly influences the development of amyloid plaques, congophilic amyloid angiopathy and subsequent tau related pathology. Relatively few AD therapeutic approaches have directly targeted the APOE-Aβ interaction thus far. Here we review the critical role of APOE in the pathogenesis of AD and some of the most promising therapeutic approaches that focus on the APOE-Aβ interaction. 2020-02-04 2020-05 /pmc/articles/PMC7118587/ /pubmed/32027932 http://dx.doi.org/10.1016/j.nbd.2020.104784 Text en https://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/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Wisniewski, Thomas
Drummond, Eleanor
APOE-amyloid interaction: Therapeutic targets
title APOE-amyloid interaction: Therapeutic targets
title_full APOE-amyloid interaction: Therapeutic targets
title_fullStr APOE-amyloid interaction: Therapeutic targets
title_full_unstemmed APOE-amyloid interaction: Therapeutic targets
title_short APOE-amyloid interaction: Therapeutic targets
title_sort apoe-amyloid interaction: therapeutic targets
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118587/
https://www.ncbi.nlm.nih.gov/pubmed/32027932
http://dx.doi.org/10.1016/j.nbd.2020.104784
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