Regional neurodegeneration correlates with sleep–wake dysfunction after stroke

Author:

Gottlieb Elie12ORCID,Egorova Natalia12,Khlif Mohamed S12,Khan Wasim123,Werden Emilio12,Pase Matthew P45,Howard Mark267ORCID,Brodtmann Amy12

Affiliation:

1. The Florey Institute of Neuroscience and Mental Health, Melbourne, Victoria, Australia

2. University of Melbourne, Melbourne, Victoria, Australia

3. Department of Neuroimaging, Institute of Psychiatry, Psychology, and Neuroscience (IoPPN), King’s College, London, UK

4. Turner Institute for Brain and Mental Health, School of Psychological Sciences, Monash University, Melbourne, Victoria, Australia

5. Harvard T.H. Chan School of Public Health, Harvard University, MA

6. Austin Health, Heidelberg, Victoria, Australia

7. Institute for Breathing and Sleep, Heidelberg, Victoria, Australia

Abstract

Abstract Sleep–wake disruption is a key modifiable risk factor and sequela of stroke. The pathogenesis of poststroke sleep dysfunction is unclear. It is not known whether poststroke sleep pathology is due to focal infarction to sleep–wake hubs or to accelerated poststroke neurodegeneration in subcortical structures after stroke. We characterize the first prospective poststroke regional brain volumetric and whole-brain, fiber-specific, white matter markers of objectively measured sleep–wake dysfunction. We hypothesized that excessively long sleep (>8 h) duration and poor sleep efficiency (<80%) measured using the SenseWear Armband 3-months poststroke (n = 112) would be associated with reduced regional brain volumes of a priori-selected sleep–wake regions of interest when compared to healthy controls with optimal sleep characteristics (n = 35). We utilized a novel technique known as a whole-brain fixel-based analysis to investigate the fiber-specific white matter differences in participants with long sleep duration. Stroke participants with long sleep (n = 24) duration exhibited reduced regional volumes of the ipsilesional thalamus and contralesional amygdala when compared with controls. Poor sleep efficiency after stroke (n = 29) was associated with reduced ipsilesional thalamus, contralesional hippocampus, and contralesional amygdala volumes. Whole-brain fixel-based analyses revealed widespread macrostructural degeneration to the corticopontocerebellar tract in stroke participants with long sleep duration, with fiber reductions of up to 40%. Neurodegeneration to subcortical structures, which appear to be vulnerable to accelerated brain volume loss after stroke, may drive sleep–wake deficiencies poststroke, independent of lesion characteristics and confounding comorbidities. We discuss these findings in the context of the clinicopathological implications of sleep-related neurodegeneration and attempt to corroborate previous mechanistic-neuroanatomical findings.

Funder

National Health and Medical Research Council

Brain Foundation

Wicking Trust

Collie Trust

Sidney and Fiona Myer Family Foundation

Australian Research Council Discovery Early Career Researcher

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Neurology (clinical)

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