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Sleep, 24-h activity rhythms, and plasma markers of neurodegenerative disease
Sleep and 24-h activity rhythm disturbances are associated with development of neurodegenerative diseases and related pathophysiological processes in the brain. We determined the cross-sectional relation of sleep and 24-h activity rhythm disturbances with plasma-based biomarkers that might signal ne...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7692474/ https://www.ncbi.nlm.nih.gov/pubmed/33244083 http://dx.doi.org/10.1038/s41598-020-77830-4 |
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author | Lysen, Thom S. Ikram, M. Arfan Ghanbari, Mohsen Luik, Annemarie I. |
author_facet | Lysen, Thom S. Ikram, M. Arfan Ghanbari, Mohsen Luik, Annemarie I. |
author_sort | Lysen, Thom S. |
collection | PubMed |
description | Sleep and 24-h activity rhythm disturbances are associated with development of neurodegenerative diseases and related pathophysiological processes in the brain. We determined the cross-sectional relation of sleep and 24-h activity rhythm disturbances with plasma-based biomarkers that might signal neurodegenerative disease, in 4712 middle-aged and elderly non-demented persons. Sleep and activity rhythms were measured using the Pittsburgh Sleep Quality Index and actigraphy. Simoa assays were used to measure plasma levels of neurofilament light chain, and additionally β-amyloid 40, β-amyloid 42, and total-tau. We used linear regression, adjusting for relevant confounders, and corrected for multiple testing. We found no associations of self-rated sleep, actigraphy-estimated sleep and 24-h activity rhythms with neurofilament light chain after confounder adjustment and correction for multiple testing, except for a non-linear association of self-rated time in bed with neurofilament light chain (P = 2.5*10(−4)). Similarly, we observed no significant associations with β-amyloid 40, β-amyloid 42, and total-tau after multiple testing correction. We conclude that sleep and 24-h activity rhythm disturbances were not consistently associated with neuronal damage as indicated by plasma neurofilament light chain in this population-based sample middle-aged and elderly non-demented persons. Further studies are needed to determine the associations of sleep and 24-h activity rhythm disturbances with NfL-related neuronal damage. |
format | Online Article Text |
id | pubmed-7692474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76924742020-11-30 Sleep, 24-h activity rhythms, and plasma markers of neurodegenerative disease Lysen, Thom S. Ikram, M. Arfan Ghanbari, Mohsen Luik, Annemarie I. Sci Rep Article Sleep and 24-h activity rhythm disturbances are associated with development of neurodegenerative diseases and related pathophysiological processes in the brain. We determined the cross-sectional relation of sleep and 24-h activity rhythm disturbances with plasma-based biomarkers that might signal neurodegenerative disease, in 4712 middle-aged and elderly non-demented persons. Sleep and activity rhythms were measured using the Pittsburgh Sleep Quality Index and actigraphy. Simoa assays were used to measure plasma levels of neurofilament light chain, and additionally β-amyloid 40, β-amyloid 42, and total-tau. We used linear regression, adjusting for relevant confounders, and corrected for multiple testing. We found no associations of self-rated sleep, actigraphy-estimated sleep and 24-h activity rhythms with neurofilament light chain after confounder adjustment and correction for multiple testing, except for a non-linear association of self-rated time in bed with neurofilament light chain (P = 2.5*10(−4)). Similarly, we observed no significant associations with β-amyloid 40, β-amyloid 42, and total-tau after multiple testing correction. We conclude that sleep and 24-h activity rhythm disturbances were not consistently associated with neuronal damage as indicated by plasma neurofilament light chain in this population-based sample middle-aged and elderly non-demented persons. Further studies are needed to determine the associations of sleep and 24-h activity rhythm disturbances with NfL-related neuronal damage. Nature Publishing Group UK 2020-11-26 /pmc/articles/PMC7692474/ /pubmed/33244083 http://dx.doi.org/10.1038/s41598-020-77830-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lysen, Thom S. Ikram, M. Arfan Ghanbari, Mohsen Luik, Annemarie I. Sleep, 24-h activity rhythms, and plasma markers of neurodegenerative disease |
title | Sleep, 24-h activity rhythms, and plasma markers of neurodegenerative disease |
title_full | Sleep, 24-h activity rhythms, and plasma markers of neurodegenerative disease |
title_fullStr | Sleep, 24-h activity rhythms, and plasma markers of neurodegenerative disease |
title_full_unstemmed | Sleep, 24-h activity rhythms, and plasma markers of neurodegenerative disease |
title_short | Sleep, 24-h activity rhythms, and plasma markers of neurodegenerative disease |
title_sort | sleep, 24-h activity rhythms, and plasma markers of neurodegenerative disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7692474/ https://www.ncbi.nlm.nih.gov/pubmed/33244083 http://dx.doi.org/10.1038/s41598-020-77830-4 |
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