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A Hypnic Hypothesis of Alzheimer's Disease

BACKGROUND: Understanding the pathophysiology of Alzheimer's disease (AD) is of fundamental importance for improved diagnosis, monitoring and ultimately, treatment. OBJECTIVE: A role for the sleep-wake cycle in the pathogenesis of AD has been proposed, but remains to be worked out in detail. ME...

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Detalles Bibliográficos
Autores principales: Clark, Camilla N., Warren, Jason D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884167/
https://www.ncbi.nlm.nih.gov/pubmed/23635607
http://dx.doi.org/10.1159/000350060
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author Clark, Camilla N.
Warren, Jason D.
author_facet Clark, Camilla N.
Warren, Jason D.
author_sort Clark, Camilla N.
collection PubMed
description BACKGROUND: Understanding the pathophysiology of Alzheimer's disease (AD) is of fundamental importance for improved diagnosis, monitoring and ultimately, treatment. OBJECTIVE: A role for the sleep-wake cycle in the pathogenesis of AD has been proposed, but remains to be worked out in detail. METHODS: Here we draw together several lines of previous work to outline a ‘hypnic hypothesis’ of AD. RESULTS: We propose that altered function of brainstem neurotransmitter pathways associated with sleep, promotes regionally specific disintegration of a cortico-subcortical ‘default mode’ brain network that is selectively vulnerable in AD. CONCLUSION: The formation of a dynamic toxic state within this vulnerable network linked to sleep-wake disruption, would in turn lead to failure of synaptic repair, increased transmission of pathogenic misfolded proteins and a self-amplifying neurodegenerative process. We consider the evidence for this hypnic hypothesis and the implications that follow on from it.
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spelling pubmed-38841672014-01-22 A Hypnic Hypothesis of Alzheimer's Disease Clark, Camilla N. Warren, Jason D. Neurodegener Dis Review BACKGROUND: Understanding the pathophysiology of Alzheimer's disease (AD) is of fundamental importance for improved diagnosis, monitoring and ultimately, treatment. OBJECTIVE: A role for the sleep-wake cycle in the pathogenesis of AD has been proposed, but remains to be worked out in detail. METHODS: Here we draw together several lines of previous work to outline a ‘hypnic hypothesis’ of AD. RESULTS: We propose that altered function of brainstem neurotransmitter pathways associated with sleep, promotes regionally specific disintegration of a cortico-subcortical ‘default mode’ brain network that is selectively vulnerable in AD. CONCLUSION: The formation of a dynamic toxic state within this vulnerable network linked to sleep-wake disruption, would in turn lead to failure of synaptic repair, increased transmission of pathogenic misfolded proteins and a self-amplifying neurodegenerative process. We consider the evidence for this hypnic hypothesis and the implications that follow on from it. S. Karger AG 2013-10 2013-04-26 /pmc/articles/PMC3884167/ /pubmed/23635607 http://dx.doi.org/10.1159/000350060 Text en Copyright © 2013 by S. Karger AG, Basel http://creativecommons.org/licenses/by/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution 3.0 Unported license (CC BY 3.0) (www.karger.com/OA-license-WT), applicable to the online version of the article only. Users may download, print and share this work on the Internet, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions.
spellingShingle Review
Clark, Camilla N.
Warren, Jason D.
A Hypnic Hypothesis of Alzheimer's Disease
title A Hypnic Hypothesis of Alzheimer's Disease
title_full A Hypnic Hypothesis of Alzheimer's Disease
title_fullStr A Hypnic Hypothesis of Alzheimer's Disease
title_full_unstemmed A Hypnic Hypothesis of Alzheimer's Disease
title_short A Hypnic Hypothesis of Alzheimer's Disease
title_sort hypnic hypothesis of alzheimer's disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884167/
https://www.ncbi.nlm.nih.gov/pubmed/23635607
http://dx.doi.org/10.1159/000350060
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