Associations of Sleep Characteristics with Cerebrospinal Fluid sTREM2 in Cognitively Normal Older Adults: the CABLE Study

被引:7
作者
Hu, He-Ying [1 ]
Ma, Ling-Zhi [1 ]
Hu, Hao [1 ]
Bi, Yan-Lin [2 ]
Ma, Ya-Hui [1 ]
Shen, Xue-Ning [3 ,4 ]
Ou, Ya-Nan [1 ]
Dong, Qiang [3 ,4 ]
Tan, Lan [1 ]
Yu, Jin-Tai [3 ,4 ]
机构
[1] Qingdao Univ, Qingdao Municipal Hosp, Dept Neurol, Qingdao, Peoples R China
[2] Qingdao Univ, Qingdao Municipal Hosp, Dept Anesthesiol, Qingdao, Peoples R China
[3] Fudan Univ, Shanghai Med Coll, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China
[4] Fudan Univ, Shanghai Med Coll, Huashan Hosp, Inst Neurol, Shanghai, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Sleep; Cerebrospinal fluid; sTREM2; Microglia; Inflammation; Amyloid; PRECLINICAL ALZHEIMER-DISEASE; MICROGLIAL ACTIVATION; QUALITY; DURATION; BURDEN;
D O I
10.1007/s12640-021-00383-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:1372 / 1380
页数:9
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