Department of Neurology, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
College of Medicine and Pharmaceutics, Ocean University of China, Qingdao, China.
J Alzheimers Dis. 2021;84(3):1029-1038. doi: 10.3233/JAD-215017.
The associations between sleep characteristics and cognition are complicated. Alzheimer's disease (AD) pathologies have been proven to be associated with sleep characteristics.
We aimed to investigate the associations between sleep characteristics and cognitive function and examine the roles of AD pathologies in modulating the association of sleep duration with cognition.
A total of 974 participants who had measurements of cerebrospinal fluid (CSF) amyloid-β (Aβ), phosphorylated tau (P-tau), total tau proteins (T-tau), cognitive function, and sleep characteristics were included from the Chinese Alzheimer's Biomarker and Lifestyle (CABLE) study. Linear regression analyses were utilized to explore the associations of sleep characteristics with cognition. Non-linear regression analyses were utilized to explore the associations of sleep habits with cognition. Causal mediation analyses were conducted to explore the mediation effects of AD pathologies on cognition.
The Pittsburgh Sleep Quality Index (PSQI) total score was significantly negatively correlated with Montreal Cognitive Assessment (MoCA) score (p = 0.0176). Long latency (p = 0.0054) and low efficiency (p = 0.0273) were associated with cognitive impairment. Habitual nap behavior was associated with lower MoCA scores (p = 0.0045). U-shaped associations were observed between sleep habits (bedtime and nocturnal sleep duration) and cognition. A causal mediation analysis indicated that P-tau/Aβ42 mediated the association of sleep duration with cognition.
These findings showed sleep characteristics were associated with cognitive functions. Sleep habits (duration, bedtime) had U-shaped associations with cognition. AD core pathologies might partially mediate the influence of sleep duration on cognitive impairments.
睡眠特征与认知之间的关系很复杂。阿尔茨海默病(AD)的病理学已被证明与睡眠特征有关。
我们旨在研究睡眠特征与认知功能之间的关系,并探讨 AD 病理学在调节睡眠持续时间与认知之间关系中的作用。
我们从中国阿尔茨海默病生物标志物和生活方式(CABLE)研究中纳入了 974 名接受脑脊液(CSF)淀粉样蛋白-β(Aβ)、磷酸化 tau(P-tau)、总 tau 蛋白(T-tau)、认知功能和睡眠特征测量的参与者。我们利用线性回归分析来探讨睡眠特征与认知之间的关系。我们利用非线性回归分析来探讨睡眠习惯与认知之间的关系。我们进行了因果中介分析,以探讨 AD 病理学对认知的中介作用。
匹兹堡睡眠质量指数(PSQI)总分与蒙特利尔认知评估(MoCA)评分呈显著负相关(p=0.0176)。潜伏期长(p=0.0054)和效率低(p=0.0273)与认知障碍有关。习惯性午睡行为与较低的 MoCA 评分有关(p=0.0045)。睡眠习惯(就寝时间和夜间睡眠时间)与认知之间存在 U 形关联。因果中介分析表明,P-tau/Aβ42 介导了睡眠持续时间与认知之间的关系。
这些发现表明睡眠特征与认知功能有关。睡眠习惯(持续时间、就寝时间)与认知呈 U 形关联。AD 核心病理学可能部分介导了睡眠持续时间对认知障碍的影响。