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A [11C]PBR28 PET study on the associations between sleep health and microglial density
Leonie Jt Balter1,2,3,4, Jonatan Malmros5,6, Per Stenkrona7
1Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, 171 65, Sweden. leonie.balter@ki.se.
Abstract:
Sleep disturbances and inflammation are interconnected through shared regulatory mechanisms and are both implicated in age-related diseases. However, their connection at the level of brain-specific inflammation remains underexamined in humans. This study investigated whether specific dimensions of sleep are associated with microglial density, as measured by translocator protein (TSPO) levels, a biomarker of neuroinflammation. TSPO levels were measured using a single [11C]PBR28 positron emission tomography (PET) scan in 39 healthy adults aged 50-81 years (Mage = 66.7, SD = 8.9; 19 females, 20 males). Sleep dimensions were assessed using the Karolinska Sleep Questionnaire on three occasions over five years, twice before and once around the time of PET imaging. Shorter sleep, more frequent napping, daytime fatigue, and sleep insufficiency were associated with higher TSPO levels in the middle frontal cortex (MFC). Conversely, longer sleep was associated with higher TSPO levels in the hippocampus and putamen. Exploratory factor analysis and bootstrapping confirmed a negative association between a factor representing shorter sleep and MFC TSPO levels. Additionally, a greater deviation from optimal sleep duration over the five years, in either direction from eight hours, was associated with higher current TSPO levels in all but one examined brain regions. Peripheral C-reactive protein levels did not significantly correlate with the sleep variables or TSPO levels in any of the brain regions. Analyses were adjusted for age and sex. These findings suggest that insufficient and prolonged sleep durations are associated with elevated microglial density in frontostriatal and limbic systems, respectively, among healthy middle-aged and older adults, without any associations with peripheral inflammation. Further longitudinal studies are needed to clarify directionality and whether changes in sleep duration over time may serve as early indicators of brain health.
Insights
Sleep disturbances like shorter sleep duration and fatigue are linked to increased brain inflammation (microglial density) in older adults. This connection exists independently of peripheral inflammation markers.
Area of Science:
- Neuroscience
- Gerontology
- Sleep Medicine
Background:
- Sleep disturbances and inflammation are linked to age-related diseases.
- Brain-specific inflammation's connection to sleep is not well understood in humans.
- Microglial density, a marker of neuroinflammation, is measurable via translocator protein (TSPO) levels.
Purpose of the Study:
- To investigate the association between specific sleep dimensions and microglial density in healthy older adults.
- To explore the relationship between sleep patterns and TSPO levels in brain regions.
Main Methods:
- 39 healthy adults (50-81 years) underwent [11C]PBR28 positron emission tomography (PET) scans.
- Sleep dimensions were assessed using the Karolinska Sleep Questionnaire over five years.
- TSPO levels were measured as a biomarker of neuroinflammation.
Main Results:
- Shorter sleep, napping, fatigue, and sleep insufficiency correlated with higher TSPO in the middle frontal cortex (MFC).
- Longer sleep correlated with higher TSPO in the hippocampus and putamen.
- Greater deviation from 8-hour sleep duration was linked to higher TSPO across brain regions.
Conclusions:
- Insufficient and prolonged sleep are associated with elevated microglial density in specific brain systems in older adults.
- No significant association was found between sleep variables and peripheral inflammation (C-reactive protein).
- Longitudinal studies are needed to confirm causality and sleep duration's role as an early brain health indicator.
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