4.6 Article

The Relationship between Sleep Quality and Brain Amyloid Burden

期刊

SLEEP
卷 39, 期 5, 页码 1063-1068

出版社

OXFORD UNIV PRESS INC
DOI: 10.5665/sleep.5756

关键词

Alzheimer disease; apolipoprotein epsilon 4 allele; beta-amyloid; sleep; sleep latency

资金

  1. CSIRO Flagship Collaboration Fund
  2. Science and Industry Endowment Fund (SIEF)
  3. Edith Cowan University (ECU)
  4. Florey Institute of Neuroscience and Mental Health
  5. Alzheimer's Australia (AA)
  6. National Ageing Research Institute (NARI)
  7. Austin Health
  8. CogState Ltd.
  9. Hollywood Private Hospital
  10. Sir Charles Gairdner Hospital
  11. National Health and Medical Research Council (NHMRC)
  12. Dementia Collaborative Research Centres program (DCRC2)
  13. McCusker Alzheimer's Research Foundation
  14. Government of Victoria

向作者/读者索取更多资源

Study Objectives: To evaluate the association between self-reported sleep quality and levels of brain beta-amyloid (A beta) burden, and to determine the effect of the apolipoprotein E (APOE) epsilon 4 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 A beta positron emission tomography imaging for the quantification of brain A beta burden and were APOE genotyped. Linear regression analyses were used to evaluate the relationship between sleep quality factors and brain A beta burden, adjusting for age, body mass index, cardiovascular disease, and symptoms of depression, with APOE epsilon 4 carriage entered as a moderator. Results: Of the sleep factors, longer sleep latency was associated with higher levels of brain A beta (B = 0.003 [standard error = 0.001], P = 0.02). APOE epsilon 4 allele (carrier/noncarrier) did not moderate the relationship between sleep latency and brain A beta burden. Conclusions: Our findings suggest a relationship between brain A beta burden and sleep latency, independent of APOE epsilon 4 genotype.

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