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Sleep Disruption and Its Impact on Brain Blood Vessels and Dementia Risk

Sleep Disruption and Its Impact on Brain Blood Vessels and Dementia Risk

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Fragmented sleep can damage brain blood vessels and increase the risk of dementia. A new study reveals cellular changes linked to sleep disturbance that accelerate cognitive decline in older adults.

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Recent research highlights the detrimental effects of disrupted sleep on brain health, particularly on blood vessels within the brain. The study, published in the journal Brain, provides new cellular and molecular evidence that poor sleep quality directly harms brain blood vessels and impairs blood flow, which may elevate the risk of developing dementia.

The investigation focused on older adults, utilizing wearable sensors to monitor sleep patterns and advanced gene sequencing to analyze brain tissue post-mortem. Researchers observed that individuals experiencing fragmented sleep—characterized by restlessness and frequent awakenings—exhibited alterations in pericytes. These cells are crucial for regulating blood flow and controlling substance exchange between blood and brain tissue.

The key finding was that sleep fragmentation was associated with a decrease in pericyte function, leading to cellular damage in brain vasculature. This damage correlates with a faster decline in cognitive abilities in the years leading up to death, suggesting a link between poor sleep and neurodegeneration.

Andrew Lim, a sleep neurologist at Sunnybrook Health Sciences Centre and lead investigator, explained that these changes might represent a mechanism by which sleep disturbances contribute to small vessel disease and cognitive decline. The study emphasizes that targeting sleep quality and pericyte health could offer new avenues for preventing or slowing dementia progression.

The results reinforce the importance of good sleep hygiene, especially in aging populations, and open up new possibilities for therapeutic interventions that focus on vascular health within the brain to combat cognitive impairments associated with dementia.

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