The prospective association of objectively measured sleep and cerebral white matter microstructure in middle-aged and older persons

Author:

Kocevska Desana123,Tiemeier Henning124,Lysen Thom S1,de Groot Marius156ORCID,Muetzel Ryan L12,Van Someren Eus J W378,Ikram M Arfan19,Vernooij Meike W15,Luik Annemarie I1

Affiliation:

1. Department of Epidemiology, Erasmus MC University Medical Center, Rotterdam, the Netherlands

2. Department of Child and Adolescent Psychiatry, Erasmus MC University Medical Center, Rotterdam, the Netherlands

3. Department of Sleep and Cognition, Netherlands Institute for Neuroscience (an Institute of the Royal Netherlands Academy of Arts and Sciences), Amsterdam, The Netherlands

4. Department of Social and Behavioral Science, Harvard TH Chan School of Public Health, Boston, MA

5. Department of Radiology and Nuclear Medicine, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands

6. Department of Medical Informatics, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands

7. Department of Integrative Neurophysiology, Centre for Neurogenomics and Cognitive Research, VU University Medical Centre, Amsterdam, The Netherlands

8. Department of Psychiatry, Centre for Neurogenomics and Cognitive Research, VU University Medical Centre, Amsterdam, The Netherlands

9. Department of Neurology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands

Abstract

AbstractStudy ObjectivesPoor sleep may destabilize axonal integrity and deteriorate cerebral white matter. In middle-aged and older adults sleep problems increase alongside structural brain changes, but the temporal relation between these processes is poorly understood. We studied longitudinal associations between sleep and cerebral white matter microstructure.MethodsOne thousand one persons (59.3 ± 7.9 years, 55% women) were followed across 5.8 years (3.9–10.8). Total sleep time (TST, hours), sleep efficiency (SE, percentage), sleep onset latency (SOL, minutes), and wake after sleep onset (WASO, minutes) were measured at baseline using a wrist-worn actigraph. White matter microstructure (global and tract-specific fractional anisotropy [FA] and mean diffusivity [MD]) was measured twice with diffusion tensor imaging (DTI).ResultsPoor sleep was associated with worse white matter microstructure up to 7 years later but did not predict trajectories of DTI over time. Longer TST was associated with higher global FA (β = 0.06, 95% CI: 0.01 to 0.12), but not with MD. Persons with higher SE had higher global FA (β = 0.01, 95% CI: 0.002 to 0.01) and lower MD (β = −0.01, 95% CI: −0.01 to −0.0004). Consistently, those with more WASO had lower global FA (β = −0.003, 95% CI: −0.005 to −0.001) and higher MD (β = 0.002, 95% CI: 0.0004 to 0.004). Global findings seemed to be driven by microstructural alterations in the cingulum, anterior forceps of corpus callosum, projection and association tracts.ConclusionsMiddle-aged and older persons with more WASO, lower SE and shorter TST have worse microstructure of cerebral white matter. Microstructural alterations are most pronounced projection and association tracts, in the cingulum, and in the anterior forceps of corpus callosum.

Funder

Netherlands Organization for Scientific Research

European Commission

Dutch Brain Foundation

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Clinical Neurology

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