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Sleep Time Estimated by an Actigraphy Watch Correlates With CSF Tau in Cognitively Unimpaired Elders: The Modulatory Role of APOE

Authors :
Sara López-García
Carmen Lage
Ana Pozueta
María García-Martínez
Martha Kazimierczak
Andrea Fernández-Rodríguez
María Bravo
Luis Reyes-González
Juan Irure
Marcos López-Hoyos
Eloy Rodríguez-Rodríguez
Pascual Sánchez-Juan
Source :
Frontiers in Aging Neuroscience, Vol 13 (2021)
Publication Year :
2021
Publisher :
Frontiers Media S.A., 2021.

Abstract

There is increasing evidence of the relationship between sleep and neurodegeneration, but this knowledge is not incorporated into clinical practice yet. We aimed to test whether a basic sleep parameter, as total sleep estimated by actigraphy for 1 week, was a valid predictor of CSF Alzheimer’s Disease core biomarkers (amyloid-β-42 and –40, phosphorylated-tau-181, and total-tau) in elderly individuals, considering possible confounders and effect modifiers, particularly the APOE ε4 allele. One hundred and twenty-seven cognitively unimpaired volunteers enrolled in the Valdecilla Study for Memory and Brain Aging participated in this study. Seventy percent of the participants were women with a mean age of 65.5 years. After adjustment for covariates, reduced sleep time significantly predicted higher t-tau and p-tau. This association was mainly due to the APOE ε4 carriers. Our findings suggest that total sleep time, estimated by an actigraphy watch, is an early biomarker of tau pathology and that APOE modulates this relationship. The main limitation of this study is the limited validation of the actigraphy technology used. Sleep monitoring with wearables may be a useful and inexpensive screening test to detect early neurodegenerative changes.

Details

Language :
English
ISSN :
16634365
Volume :
13
Database :
Directory of Open Access Journals
Journal :
Frontiers in Aging Neuroscience
Publication Type :
Academic Journal
Accession number :
edsdoj.b504afd8295a403f83f16bc39141a376
Document Type :
article
Full Text :
https://doi.org/10.3389/fnagi.2021.663446