Tsapanou A, Gao Y, Stern Y, Barral S
Cognitive Neuroscience Division, Department of Neurology, Columbia University Medical Center, New York, NY, USA.
Department of Neurology, The Gertrude H. Sergievsky Center and the Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University Medical Center, New York, NY, USA.
Sleep Med. 2020 Oct;74:262-266. doi: 10.1016/j.sleep.2020.07.001. Epub 2020 Jul 14.
Age-related changes in sleep include a reduction in total sleep time and a greater incidence of sleep disorders, and are also an integral part of neurodegenerations. In the present study, we aimed to: a) identify common genetic variants that may influence self-reported sleep duration, and b) examine the association between the identified genetic variants and performance in different cognitive domains.
A sample of 197 cognitively healthy participants, aged 20-80 years, mostly non-Hispanic Whites (69%), were selected from the Reference Abilities Neural Network and the Cognitive Reserve study. Each participant underwent an evaluation of sleep function and assessment of neuropsychological performance on global cognition and four different domains (memory, speed of processing, fluid reasoning, language). Published GWAS summary statistics from a Polygenic Score (PS) for sleep duration in a large European ancestry cohort (N = 30,251) were used to derive a PS in our study sample. Multivariate linear models were used to test the associations between the PS and sleep duration and cognitive performance. Age, sex, and education were used as covariates. Secondary analyses were conducted in three age-groups (young, middle, old).
Higher PS was linked to longer sleep duration and was also associated with better performance in global cognition, fluid reasoning, speed of processing, and language, but not memory. Results especially for fluid reasoning, language, and global cognition were driven mostly by the young group.
Our study replicated the previously reported association between sleep-PS and longer sleep duration. We additionally found a significant association between the sleep-PS and cognitive function. Our results suggest that common genetic variants may influence the link between sleep duration and cognitive health.
与年龄相关的睡眠变化包括总睡眠时间减少和睡眠障碍发生率增加,并且也是神经退行性变的一个组成部分。在本研究中,我们旨在:a)识别可能影响自我报告睡眠时间的常见基因变异,以及b)检查所识别的基因变异与不同认知领域表现之间的关联。
从参考能力神经网络和认知储备研究中选取了197名年龄在20 - 80岁之间、认知健康的参与者作为样本,其中大多数为非西班牙裔白人(69%)。每位参与者都接受了睡眠功能评估以及关于整体认知和四个不同领域(记忆、处理速度、流体推理、语言)的神经心理学表现评估。使用来自一个大型欧洲血统队列(N = 30251)中睡眠时间的多基因评分(PS)的已发表全基因组关联研究(GWAS)汇总统计数据,在我们的研究样本中得出一个PS。使用多元线性模型来测试PS与睡眠时间和认知表现之间的关联。年龄、性别和教育程度用作协变量。在三个年龄组(青年、中年、老年)中进行了二次分析。
较高的PS与较长的睡眠时间相关,并且还与整体认知、流体推理、处理速度和语言方面的更好表现相关,但与记忆无关。特别是流体推理、语言和整体认知方面的结果主要由青年组驱动。
我们的研究重复了先前报道的睡眠PS与较长睡眠时间之间的关联。我们还发现睡眠PS与认知功能之间存在显著关联。我们的结果表明,常见基因变异可能影响睡眠时间与认知健康之间的联系。