老年人日间午睡的时间和个体变异与阿尔茨海默病

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Chenlu Gao, Xi Zheng, Ruixue Cai, Lei Yu, Julie A Schneider, Aron S Buchman, David A Bennett, Yue Leng, Agustin Ibáñez, Lei Gao, Kun Hu, Peng Li
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引用次数: 0

摘要

背景:白天过多的午睡与老年人的神经变性有关,但之前的研究主要集中在午睡的时间和频率上。新兴的框架强调睡眠的多维性,但仍不清楚午睡的其他方面(如时间、变异性)是否与神经变性有关。为了解决这一差距,我们调查了白天午睡时间和午睡时间的个体变异与阿尔茨海默病和阿尔茨海默病病理的关系。方法:我们分析了936名老年人的资料(年龄范围:56-99;77%的女性)在拉什记忆和衰老项目中进行研究,以检查阿尔茨海默氏痴呆症的发病率,并从320名已故的参与者(死亡年龄范围:71-105;70%为女性)检查阿尔茨海默病病理。使用活动记录仪评估了上午(上午9-11点)和下午早些时候(下午1-3点)小睡的比例以及小睡时间的个体差异性。参与者在基线和每年完成神经学评估长达17年。在死亡的参与者中,检查了β淀粉样蛋白和神经原纤维缠结。研究结果:我们发现,早晨小睡时间越长,患阿尔茨海默氏症的风险越高,而下午小睡时间越早,β淀粉样蛋白水平越低。午睡时间的个体差异与β淀粉样蛋白和神经原纤维缠结的增加有关。结论:我们的研究结果表明,特定的时间模式和白天午睡的不规律与阿尔茨海默病的风险和病理有关。午睡行为的多维评估可能有助于神经认知障碍的风险分层,并提供旨在促进健康认知衰老的干预措施的潜在目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Timing and intraindividual variability of daytime napping and Alzheimer's disease in older adults.

Background: Excessive daytime napping has been associated with neurodegeneration in older adults, but prior research has focused on nap duration and frequency. Emerging frameworks emphasize the multidimensionality of sleep, but it remains unknown whether other dimensions of napping (e.g., timing, variability) are linked to neurodegeneration. To address this gap, we investigated the associations of daytime nap timing and intraindividual variability of nap duration with incident Alzheimer's dementia and Alzheimer's disease pathology.

Methods: We analyzed data from 936 older adults (age range: 56-99; 77% female) in the Rush Memory and Aging Project to examine incident Alzheimer's dementia and from 320 deceased participants (age range at death: 71-105; 70% female) to examine Alzheimer's pathology. The proportions of morning (9-11am) and early afternoon naps (1-3 pm) and the intraindividual variability of nap duration were assessed using actigraphy. Participants completed neurological assessments at baseline and annually for up to 17 years. In deceased participants, amyloid β and neurofibrillary tangles were examined.

Results: Here we show that more morning naps are linked to a higher risk of Alzheimer's dementia, whereas more early afternoon naps are linked to reduced amyloid β levels. Higher intraindividual variability of nap duration is shown to be associated with increased amyloid β and neurofibrillary tangles.

Conclusions: Our findings suggest that specific timing patterns and irregularities in daytime napping are linked to Alzheimer's disease risk and pathology. Multi-dimensional assessments of nap behaviors may aid in risk stratification for neurocognitive impairment and offer a potential target for interventions aimed at promoting healthy cognitive aging.

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