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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
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.
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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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