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Timely coupling of sleep spindles and slow waves linked to early amyloid-β burden and predicts memory decline
Sleep alteration is a hallmark of ageing and emerges as a risk factor for Alzheimer’s disease (AD). While the fine-tuned coalescence of sleep microstructure elements may influence age-related cognitive trajectories, its association with AD processes is not fully established. Here, we investigated wh...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9177143/ https://www.ncbi.nlm.nih.gov/pubmed/35638265 http://dx.doi.org/10.7554/eLife.78191 |
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author | Chylinski, Daphne Van Egroo, Maxime Narbutas, Justinas Muto, Vincenzo Bahri, Mohamed Ali Berthomier, Christian Salmon, Eric Bastin, Christine Phillips, Christophe Collette, Fabienne Maquet, Pierre Carrier, Julie Lina, Jean-Marc Vandewalle, Gilles |
author_facet | Chylinski, Daphne Van Egroo, Maxime Narbutas, Justinas Muto, Vincenzo Bahri, Mohamed Ali Berthomier, Christian Salmon, Eric Bastin, Christine Phillips, Christophe Collette, Fabienne Maquet, Pierre Carrier, Julie Lina, Jean-Marc Vandewalle, Gilles |
author_sort | Chylinski, Daphne |
collection | PubMed |
description | Sleep alteration is a hallmark of ageing and emerges as a risk factor for Alzheimer’s disease (AD). While the fine-tuned coalescence of sleep microstructure elements may influence age-related cognitive trajectories, its association with AD processes is not fully established. Here, we investigated whether the coupling of spindles and slow waves (SW) is associated with early amyloid-β (Aβ) brain burden, a hallmark of AD neuropathology, and cognitive change over 2 years in 100 healthy individuals in late-midlife (50–70 years; 68 women). We found that, in contrast to other sleep metrics, earlier occurrence of spindles on slow-depolarisation SW is associated with higher medial prefrontal cortex Aβ burden (p=0.014, r²(β*)=0.06) and is predictive of greater longitudinal memory decline in a large subsample (p=0.032, r²(β*)=0.07, N=66). These findings unravel early links between sleep, AD-related processes, and cognition and suggest that altered coupling of sleep microstructure elements, key to its mnesic function, contributes to poorer brain and cognitive trajectories in ageing. |
format | Online Article Text |
id | pubmed-9177143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-91771432022-06-09 Timely coupling of sleep spindles and slow waves linked to early amyloid-β burden and predicts memory decline Chylinski, Daphne Van Egroo, Maxime Narbutas, Justinas Muto, Vincenzo Bahri, Mohamed Ali Berthomier, Christian Salmon, Eric Bastin, Christine Phillips, Christophe Collette, Fabienne Maquet, Pierre Carrier, Julie Lina, Jean-Marc Vandewalle, Gilles eLife Neuroscience Sleep alteration is a hallmark of ageing and emerges as a risk factor for Alzheimer’s disease (AD). While the fine-tuned coalescence of sleep microstructure elements may influence age-related cognitive trajectories, its association with AD processes is not fully established. Here, we investigated whether the coupling of spindles and slow waves (SW) is associated with early amyloid-β (Aβ) brain burden, a hallmark of AD neuropathology, and cognitive change over 2 years in 100 healthy individuals in late-midlife (50–70 years; 68 women). We found that, in contrast to other sleep metrics, earlier occurrence of spindles on slow-depolarisation SW is associated with higher medial prefrontal cortex Aβ burden (p=0.014, r²(β*)=0.06) and is predictive of greater longitudinal memory decline in a large subsample (p=0.032, r²(β*)=0.07, N=66). These findings unravel early links between sleep, AD-related processes, and cognition and suggest that altered coupling of sleep microstructure elements, key to its mnesic function, contributes to poorer brain and cognitive trajectories in ageing. eLife Sciences Publications, Ltd 2022-05-31 /pmc/articles/PMC9177143/ /pubmed/35638265 http://dx.doi.org/10.7554/eLife.78191 Text en © 2022, Chylinski et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Chylinski, Daphne Van Egroo, Maxime Narbutas, Justinas Muto, Vincenzo Bahri, Mohamed Ali Berthomier, Christian Salmon, Eric Bastin, Christine Phillips, Christophe Collette, Fabienne Maquet, Pierre Carrier, Julie Lina, Jean-Marc Vandewalle, Gilles Timely coupling of sleep spindles and slow waves linked to early amyloid-β burden and predicts memory decline |
title | Timely coupling of sleep spindles and slow waves linked to early amyloid-β burden and predicts memory decline |
title_full | Timely coupling of sleep spindles and slow waves linked to early amyloid-β burden and predicts memory decline |
title_fullStr | Timely coupling of sleep spindles and slow waves linked to early amyloid-β burden and predicts memory decline |
title_full_unstemmed | Timely coupling of sleep spindles and slow waves linked to early amyloid-β burden and predicts memory decline |
title_short | Timely coupling of sleep spindles and slow waves linked to early amyloid-β burden and predicts memory decline |
title_sort | timely coupling of sleep spindles and slow waves linked to early amyloid-β burden and predicts memory decline |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9177143/ https://www.ncbi.nlm.nih.gov/pubmed/35638265 http://dx.doi.org/10.7554/eLife.78191 |
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