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Updated: Nov 2, 2025

Multi-Modal Home Sleep Monitoring in Older Adults
Published on: January 26, 2019
Associations of Sleep Characteristics with Cerebrospinal Fluid sTREM2 in Cognitively Normal Older Adults: the CABLE
He-Ying Hu1, Ling-Zhi Ma1, Hao Hu1
1Department of Neurology, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
Abstract:
As brain insults, sleep disorders could enhance microglial activation and aggravate neuroinflammation. Soluble triggering receptor expressed on myeloid cells 2 (sTREM2) in cerebrospinal fluid (CSF) serves as a readout for TREM2-associated microglial responses. We aimed to study the association of sleep characteristics with CSF sTREM2 in cognitively normal (CN) older adults. Linear and non-linear regression analyses were conducted in 830 participants with measurements of sleep characteristics and CSF sTREM2, after adjusting for age, sex, education, the Chinese-Modified Mini-Mental State Examination (CM-MMSE) scores, and APOE4 status. These analyses were also performed in amyloid-negative (A -) and amyloid-positive (A +) individuals. Linear relationships between sleep characteristics and CSF sTREM2 were found. In all the participants, sleep efficiency score in Pittsburgh Sleep Quality Index (PSQI) (p = 0.037) showed a positive linear association with CSF sTREM2. In A + individuals, the grade of PSQI total score (p = 0.011) as well as subjective sleep quality score (p = 0.048) and sleep efficiency score (p < 0.001) in PSQI were positively associated with CSF sTREM2. Besides, several U-shaped relationships were revealed of sleep-time measures, such as insufficient or excessive nocturnal sleep duration, with CSF sTREM2 in A + individuals (the optimal model: bedtime 22:21 p.m., time to fall asleep 22:52 p.m., nocturnal sleep duration 7.36 h). In A - individuals, the above relationships were not found. Poor self-reported sleep characteristics and sleep indicators were associated with higher CSF sTREM2, suggesting that sleep might play an important role in the regulation of TREM2-associated microglial activity.
Insights
Poor sleep quality and duration are linked to higher levels of soluble triggering receptor expressed on myeloid cells 2 (sTREM2) in cognitively normal older adults, particularly those with amyloid plaques. This suggests sleep influences neuroinflammation.
Area of Science:
- Neuroscience
- Immunology
- Sleep Medicine
Background:
- Sleep disturbances can exacerbate neuroinflammation by activating microglia.
- Soluble triggering receptor expressed on myeloid cells 2 (sTREM2) in cerebrospinal fluid (CSF) reflects microglial activity.
- Understanding the link between sleep and microglial responses is crucial for brain health.
Purpose of the Study:
- To investigate the association between sleep characteristics and CSF sTREM2 levels in cognitively normal older adults.
- To explore these associations in relation to amyloid pathology (amyloid-positive vs. amyloid-negative).
Main Methods:
- Linear and non-linear regression analyses were performed on 830 participants.
- Sleep characteristics were assessed using the Pittsburgh Sleep Quality Index (PSQI) and sleep-time measures.
- CSF sTREM2 levels were measured and analyzed alongside cognitive status and APOE4 genotype.
Main Results:
- Positive linear associations were found between sleep efficiency and CSF sTREM2 in all participants.
- In amyloid-positive individuals, poorer sleep quality and efficiency were linked to higher CSF sTREM2.
- U-shaped relationships were observed between sleep duration/timing and CSF sTREM2 in amyloid-positive individuals.
Conclusions:
- Poor self-reported sleep is associated with elevated CSF sTREM2, indicating increased microglial activity.
- Sleep plays a significant role in regulating TREM2-associated microglial responses, especially in the presence of amyloid pathology.
- These findings highlight sleep as a potential target for mitigating neuroinflammation.
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