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Sleep fragmentation, microglial aging, and cognitive impairment in adults with and without Alzheimer’s dementia
Sleep disruption is associated with cognitive decline and dementia in older adults; however, the underlying mechanisms are unclear. In rodents, sleep disruption causes microglial activation, inhibition of which improves cognition. However, data from humans are lacking. We studied participants in two...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6905859/ https://www.ncbi.nlm.nih.gov/pubmed/31844665 http://dx.doi.org/10.1126/sciadv.aax7331 |
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author | Kaneshwaran, Kirusanthy Olah, Marta Tasaki, Shinya Yu, Lei Bradshaw, Elizabeth M. Schneider, Julie A. Buchman, Aron S. Bennett, David A. De Jager, Philip L. Lim, Andrew S. P. |
author_facet | Kaneshwaran, Kirusanthy Olah, Marta Tasaki, Shinya Yu, Lei Bradshaw, Elizabeth M. Schneider, Julie A. Buchman, Aron S. Bennett, David A. De Jager, Philip L. Lim, Andrew S. P. |
author_sort | Kaneshwaran, Kirusanthy |
collection | PubMed |
description | Sleep disruption is associated with cognitive decline and dementia in older adults; however, the underlying mechanisms are unclear. In rodents, sleep disruption causes microglial activation, inhibition of which improves cognition. However, data from humans are lacking. We studied participants in two cohort studies of older persons—the Rush Memory and Aging Project and the Religious Orders Study. We assessed sleep fragmentation by actigraphy and related this to cognitive function, to neocortical microglial marker gene expression measured by RNA sequencing, and to the neocortical density of microglia assessed by immunohistochemistry. Greater sleep fragmentation was associated with higher neocortical expression of genes characteristic of aged microglia, and a higher proportion of morphologically activated microglia, independent of chronological age- and dementia-related neuropathologies. Furthermore, these were, in turn, associated with worse cognition. This suggests that sleep fragmentation is accompanied by accelerated microglial aging and activation, which may partially underlie its association with cognitive impairment. |
format | Online Article Text |
id | pubmed-6905859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-69058592019-12-16 Sleep fragmentation, microglial aging, and cognitive impairment in adults with and without Alzheimer’s dementia Kaneshwaran, Kirusanthy Olah, Marta Tasaki, Shinya Yu, Lei Bradshaw, Elizabeth M. Schneider, Julie A. Buchman, Aron S. Bennett, David A. De Jager, Philip L. Lim, Andrew S. P. Sci Adv Research Articles Sleep disruption is associated with cognitive decline and dementia in older adults; however, the underlying mechanisms are unclear. In rodents, sleep disruption causes microglial activation, inhibition of which improves cognition. However, data from humans are lacking. We studied participants in two cohort studies of older persons—the Rush Memory and Aging Project and the Religious Orders Study. We assessed sleep fragmentation by actigraphy and related this to cognitive function, to neocortical microglial marker gene expression measured by RNA sequencing, and to the neocortical density of microglia assessed by immunohistochemistry. Greater sleep fragmentation was associated with higher neocortical expression of genes characteristic of aged microglia, and a higher proportion of morphologically activated microglia, independent of chronological age- and dementia-related neuropathologies. Furthermore, these were, in turn, associated with worse cognition. This suggests that sleep fragmentation is accompanied by accelerated microglial aging and activation, which may partially underlie its association with cognitive impairment. American Association for the Advancement of Science 2019-12-11 /pmc/articles/PMC6905859/ /pubmed/31844665 http://dx.doi.org/10.1126/sciadv.aax7331 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Kaneshwaran, Kirusanthy Olah, Marta Tasaki, Shinya Yu, Lei Bradshaw, Elizabeth M. Schneider, Julie A. Buchman, Aron S. Bennett, David A. De Jager, Philip L. Lim, Andrew S. P. Sleep fragmentation, microglial aging, and cognitive impairment in adults with and without Alzheimer’s dementia |
title | Sleep fragmentation, microglial aging, and cognitive impairment in adults with and without Alzheimer’s dementia |
title_full | Sleep fragmentation, microglial aging, and cognitive impairment in adults with and without Alzheimer’s dementia |
title_fullStr | Sleep fragmentation, microglial aging, and cognitive impairment in adults with and without Alzheimer’s dementia |
title_full_unstemmed | Sleep fragmentation, microglial aging, and cognitive impairment in adults with and without Alzheimer’s dementia |
title_short | Sleep fragmentation, microglial aging, and cognitive impairment in adults with and without Alzheimer’s dementia |
title_sort | sleep fragmentation, microglial aging, and cognitive impairment in adults with and without alzheimer’s dementia |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6905859/ https://www.ncbi.nlm.nih.gov/pubmed/31844665 http://dx.doi.org/10.1126/sciadv.aax7331 |
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