The Reciprocal Interaction Between Sleep and Alzheimer's Disease
Samuel S Harris1, Tom Schwerd-Kleine1, Byung Il Lee1
1UK Dementia Research Institute at UCL, London, UK.
Advances in Experimental Medicine and Biology
|November 13, 2021
Summary
Disordered sleep patterns in neurodegenerative diseases may drive disease progression, not just result from it. Targeting sleep could offer new therapeutic avenues for conditions like Alzheimer's disease.
Area of Science:
- Neuroscience
- Sleep Medicine
- Gerontology
Background:
- Neurodegenerative diseases frequently present with disrupted sleep-wake patterns.
- Sleep disturbances were traditionally viewed as consequences of neurodegeneration in key brain regions.
- Emerging evidence suggests sleep deficits may actively contribute to disease progression.
Purpose of the Study:
- To explore the bidirectional relationship between sleep/circadian dysfunction and neurodegeneration.
- To highlight sleep as a potential therapeutic target for neurodegenerative diseases.
- To review the impact of impaired sleep on brain pathology in Alzheimer's disease.
Main Methods:
- Literature review of recent research on sleep, circadian rhythms, and neurodegeneration.
- Analysis of studies investigating the impact of sleep on neuronal activity, brain clearance, protein aggregation, and inflammation.
- Focus on research concerning Alzheimer's disease as a model neurodegenerative condition.
Main Results:
- Impaired sleep can negatively affect neuronal function and brain waste clearance.
- Sleep deficits are linked to increased pathological protein accumulation and neuroinflammation.
- A reciprocal interaction exists between disrupted sleep/circadian patterns and Alzheimer's disease pathology.
Conclusions:
- Sleep impairments may be pathophysiological drivers, not just symptoms, of neurodegenerative diseases.
- Altered sleep patterns represent potential dynamic biomarkers for proteinopathies.
- Non-invasive interventions targeting sleep may offer novel therapeutic strategies for early intervention.
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