4.7 Article

Associations Between Self-Reported Sleep Quality and White Matter in Community-Dwelling Older Adults: A Prospective Cohort Study

Journal

HUMAN BRAIN MAPPING
Volume 38, Issue 11, Pages 5465-5473

Publisher

WILEY
DOI: 10.1002/hbm.23739

Keywords

brain; cognition; diffusion tensor imaging; executive function; insomnia; magnetic resonance imaging; memory; processing speed

Funding

  1. UK Medical Research Council [G1001354, K013351]
  2. Wellcome Trust [110027/Z/15/Z]
  3. National Research Council of Brazil [211534/2013-7]
  4. National Institute for Health Research (NIHR) Oxford Biomedical Research Centre (BRC) at Oxford University Hospitals NHS Trust and the University of Oxford
  5. NIHR Oxford Health BRC
  6. HDH Wills 1965 Charitable Trust
  7. NordForsk
  8. Medical Research Council [MR/M024962/1, MC_EX_MR/N50192X/1, MR/K013351/1, G1001354, MR/L023784/1] Funding Source: researchfish
  9. Parkinson's UK [J-1403] Funding Source: researchfish
  10. MRC [MR/L023784/1, G1001354, MR/M024962/1, MR/K013351/1, MC_EX_MR/N50192X/1] Funding Source: UKRI

Ask authors/readers for more resources

Both sleep disturbances and decline in white matter microstructure are commonly observed in ageing populations, as well as in age-related psychiatric and neurological illnesses. A relationship between sleep and white matter microstructure may underlie such relationships, but few imaging studies have directly examined this hypothesis. In a study of 448 community-dwelling members of the Whitehall II Imaging Sub-Study aged between 60 and 82 years (90 female, mean age 69.2 +/- 5.1 years), we used the magnetic resonance imaging technique diffusion tensor imaging to examine the relationship between self-reported sleep quality and white matter microstructure. Poor sleep quality at the time of the diffusion tensor imaging scan was associated with reduced global fractional anisotropy and increased global axial diffusivity and radial diffusivity values, with small effect sizes. Voxel-wise analysis showed that widespread frontal-subcortical tracts, encompassing regions previously reported as altered in insomnia, were affected. Radial diffusivity findings remained significant after additional correction for demographics, general cognition, health, and lifestyle measures. No significant differences in general cognitive function, executive function, memory, or processing speed were detected between good and poor sleep quality groups. The number of times participants reported poor sleep quality over five time-points spanning a 16-year period was not associated with white matter measures. In conclusion, these data demonstrate that current sleep quality is linked to white matter microstructure. Small effect sizes may limit the extent to which poor sleep is a promising modifiable factor that may maintain, or even improve, white matter microstructure in ageing. (C) 2017 Wiley Periodicals, Inc.

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