Day‐to‐day sleep variability with Alzheimer's biomarkers in at‐risk elderly

Author:

Baril Andrée‐Ann1,Picard Cynthia1,Labonté Anne1,Sanchez Erlan2,Duclos Catherine34,Mohammediyan Béry1,Ashton Nicholas J.5678,Zetterberg Henrik59101112,Blennow Kaj59,Breitner John C. S.1,Villeneuve Sylvia1,Poirier Judes1,

Affiliation:

1. Douglas Mental Health University Institute McGill University Montreal Québec Canada

2. Sunnybrook Research Institute University of Toronto Toronto Ontario Canada

3. Hôpital du Sacré‐Coeur de Montréal CIUSSS‐NIM Montréal Québec Canada

4. Department of Anesthesiology and Pain Medicine Université de Montréal Montréal Québec Canada

5. Department of Psychiatry and Neurochemistry Institute of Neuroscience & Physiology the Sahlgrenska Academy at the University of Gothenburg Mölndal Sweden

6. King's College London Institute of Psychiatry Psychology and Neuroscience Maurice Wohl Institute Clinical Neuroscience Institute London UK

7. NIHR Biomedical Research Centre for Mental Health and Biomedical Research Unit for Dementia at South London and Maudsley NHS Foundation London UK

8. Centre for Age‐Related Medicine Stavanger University Hospital Stavanger Norway

9. Clinical Neurochemistry Laboratory Sahlgrenska University Hospital Mölndal Sweden

10. Department of Neurodegenerative Disease UCL Institute of Neurology Queen Square London UK

11. UK Dementia Research Institute at UCL London UK

12. Hong Kong Center for Neurodegenerative Diseases Clear Water Bay Hong Kong China

Abstract

AbstractINTRODUCTIONMeasuring day‐to‐day sleep variability might reveal unstable sleep‐wake cycles reflecting neurodegenerative processes. We evaluated the association between Alzheimer's disease (AD) fluid biomarkers with day‐to‐day sleep variability.METHODSIn the PREVENT‐AD cohort, 203 dementia‐free participants (age: 68.3 ± 5.4; 78 males) with a parental history of sporadic AD were tested with actigraphy and fluid biomarkers. Day‐to‐day variability (standard deviations over a week) was assessed for sleep midpoint, duration, efficiency, and nighttime activity count.RESULTSLower cerebrospinal fluid (CSF) ApoE, higher CSF p‐tau181/amyloid‐β (Aβ)42, and higher plasma p‐tau231/Aβ42 were associated with higher variability of sleep midpoint, sleep duration, and/or activity count. The associations between fluid biomarkers with greater sleep duration variability were especially observed in those that carried the APOE4 allele, mild cognitive impairment converters, or those with gray matter atrophy.DISCUSSIONDay‐to‐day sleep variability were associated with biomarkers of AD in at‐risk individuals, suggesting that unstable sleep promotes neurodegeneration or, conversely, that AD neuropathology disrupts sleep‐wake cycles.

Funder

Natural Sciences and Engineering Research Council of Canada

Fondation Brain Canada

Canadian Institutes of Health Research

Publisher

Wiley

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