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Age differences in the association between sleep and Alzheimer's disease biomarkers in the EPAD cohort

INTRODUCTION: We aimed to determine the independent association between sleep quality and Alzheimer's disease (AD) biomarkers, and whether the associations differ with age. METHODS: We included 1240 individuals aged ≥50, without dementia from the European Prevention of Alzheimer's Disease...

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Detalles Bibliográficos
Autores principales: Naismith, Sharon L., Leng, Yue, Palmer, Jake R., Lucey, Brendan P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9695753/
https://www.ncbi.nlm.nih.gov/pubmed/36447477
http://dx.doi.org/10.1002/dad2.12380
Descripción
Sumario:INTRODUCTION: We aimed to determine the independent association between sleep quality and Alzheimer's disease (AD) biomarkers, and whether the associations differ with age. METHODS: We included 1240 individuals aged ≥50, without dementia from the European Prevention of Alzheimer's Disease v1500.0 dataset. Linear regression was used to examine Pittsburgh Sleep Quality Index (PSQI) scores against cerebrospinal fluid (CSF) phosphorylated tau/β‐amyloid ratio (p‐tau/Aβ42) for the entire sample and via age tertiles. Models controlled for demographic, clinical, genetic, vascular, and neuroimaging variables. RESULTS: For the youngest age tertile, shorter sleep duration and higher sleep efficiency were associated with greater p‐tau/Aβ42 ratio. For the oldest tertile, longer sleep latency was associated with greater p‐tau/Aβ42. DISCUSSION: Differential relationships between sleep and AD pathology depend on age. Short sleep duration and sleep efficiency are relevant in middle age whereas time taken to fall asleep is more closely linked to AD biomarkers in later life. HIGHLIGHTS: This study shows age differences in the link between sleep and AD biomarkers. Shorter sleep was associated with greater p‐tau/Aβ42 ratio in middle age. The association was independent of genetic, vascular, and neuroimaging markers of AD.