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Title: | The relationship between sleep quality and brain amyloid burden | Austin Authors: | Brown, Belinda M;Rainey-Smith, Stephanie R;Villemagne, Victor L ;Weinborn, Michael;Bucks, Romola S;Sohrabi, Hamid R;Laws, Simon M;Taddei, Kevin;Macaulay, S Lance;Ames, David;Fowler, Christopher J;Maruff, Paul;Masters, Colin L ;Rowe, Christopher C ;Martins, Ralph N;The AIBL Research Group | Affiliation: | Department of Nuclear Medicine and Centre for PET, Austin Health, Heidelberg, Victoria, Australia School of Medical Sciences, Edith Cowan University, Joondalup, Western Australia Sir James McCusker Alzheimer's Disease Research Unit, Hollywood Private Hospital, Nedlands, Western Australia School of Psychology, University of Western Australia, Crawley, Western Australia CSIRO Food and Nutrition, Parkville, Victoria, Australia Department of Psychiatry, The University of Melbourne, Victoria, Australia National Ageing Research Institute, Parkville, Victoria, Australia Florey Institute for Neurosciences and Mental Health, University of Melbourne, Victoria, Australia Cogstate Ltd., Melbourne, Victoria, Australia School of Psychiatry and Clinical Neurosciences, University of Western Australia, Nedlands, Western Australia |
Issue Date: | 1-May-2016 | Publication information: | Sleep 2016; 39(5): 1063-1068 | Abstract: | STUDY OBJECTIVES: To evaluate the association between self-reported sleep quality and levels of brain β-amyloid (Aβ) burden, and to determine the effect of the apolipoprotein E (APOE) ε4 allele on any associations found. METHODS: This study is a cross-sectional analysis of 184 cognitively healthy men and women aged over 60 y. We measured sleep quality factors: specifically, sleep duration, latency (time taken to fall asleep), disturbances, efficiency, daytime dysfunction, and overall sleep quality, using the Pittsburgh Sleep Quality Index. All participants underwent Aβ positron emission tomography imaging for the quantification of brain Aβ burden and were APOE genotyped. Linear regression analyses were used to evaluate the relationship between sleep quality factors and brain Aβ burden, adjusting for age, body mass index, cardiovascular disease, and symptoms of depression, with APOE ε4 carriage entered as a moderator. RESULTS: Of the sleep factors, longer sleep latency was associated with higher levels of brain Aβ (B = 0.003 [standard error = 0.001], P = 0.02). APOE ε4 allele (carrier/noncarrier) did not moderate the relationship between sleep latency and brain Aβ burden. CONCLUSIONS: Our findings suggest a relationship between brain Aβ burden and sleep latency, independent of APOE ε4 genotype. | URI: | https://ahro.austin.org.au/austinjspui/handle/1/16870 | DOI: | 10.5665/sleep.5756 | ORCID: | 0000-0003-3910-2453 | Journal: | Sleep | PubMed URL: | https://pubmed.ncbi.nlm.nih.gov/27091528 | Type: | Journal Article | Subjects: | Alzheimer disease Apolipoprotein ε4 allele Beta-amyloid Sleep Sleep latency |
Appears in Collections: | Journal articles |
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