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Self-reported Sleep Problems Related to Amyloid Deposition in Cortical Regions with High HOMER1 Gene Expression.

Authors :
Fjell AM
Sederevicius D
Sneve MH
de Lange AG
Bråthen AC
Idland AV
Watne LO
Wang Y
Reinbold C
Dobricic V
Kilpert F
Blennow K
Zetterbergj H
Hong S
Bertram L
Walhovd KB
Source :
Cerebral cortex (New York, N.Y. : 1991) [Cereb Cortex] 2020 Apr 14; Vol. 30 (4), pp. 2144-2156.
Publication Year :
2020

Abstract

Sleep problems are related to the elevated levels of the Alzheimer's disease (AD) biomarker β-amyloid (Aβ). Hypotheses about the causes of this relationship can be generated from molecular markers of sleep problems identified in rodents. A major marker of sleep deprivation is Homer1a, a neural protein coded by the HOMER1 gene, which has also been implicated in brain Aβ accumulation. Here, we tested whether the relationship between cortical Aβ accumulation and self-reported sleep quality, as well as changes in sleep quality over 3 years, was stronger in cortical regions with high HOMER1 mRNA expression levels. In a sample of 154 cognitively healthy older adults, Aβ correlated with poorer sleep quality cross-sectionally and longitudinally (n = 62), but more strongly in the younger than in older individuals. Effects were mainly found in regions with high expression of HOMER1. The anatomical distribution of the sleep-Aβ relationship followed closely the Aβ accumulation pattern in 69 patients with mild cognitive impairment or AD. Thus, the results indicate that the relationship between sleep problems and Aβ accumulation may involve Homer1 activity in the cortical regions, where harbor Aβ deposits in AD. The findings may advance our understanding of the relationship between sleep problems and AD risk.<br /> (© The Author(s) 2019. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permission@oup.com.)

Details

Language :
English
ISSN :
1460-2199
Volume :
30
Issue :
4
Database :
MEDLINE
Journal :
Cerebral cortex (New York, N.Y. : 1991)
Publication Type :
Academic Journal
Accession number :
32142100
Full Text :
https://doi.org/10.1093/cercor/bhz228