Five-Year Changes in 24-Hour Sleep-Wake Activity and Dementia Risk in Oldest Old Women.

IF 8.5 1区 医学 Q1 CLINICAL NEUROLOGY Neurology Pub Date : 2025-04-22 Epub Date: 2025-03-19 DOI:10.1212/WNL.0000000000213403
Sasha Milton, Clémence Cavaillès, Sonia Ancoli-Israel, Katie L Stone, Kristine Yaffe, Yue Leng
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Abstract

Background and objectives: Sleep disruptions are associated with cognitive aging in older adults. However, little is known about longitudinal sleep changes in the oldest old and whether these changes are linked to cognitive impairment. We aimed to determine whether changes in 24-hour multidimensional sleep-wake activity are associated with mild cognitive impairment (MCI) and dementia in oldest old women.

Methods: We studied cognitively unimpaired women enrolled in the Study of Osteoporotic Fractures who completed wrist actigraphy twice (baseline and follow-up) and had cognitive status evaluated at follow-up using a neuropsychological battery and adjudication. To identify multidimensional sleep-wake change profiles, we performed hierarchical clustering on principal components on the 5-year changes (median 5.0 [range 3.5-6.3] years) in nighttime sleep (sleep duration, sleep efficiency [SE], and wake after sleep onset [WASO]), napping (duration and frequency), and circadian rest-activity rhythms (RARs; acrophase, amplitude, mesor, and robustness). Using multinomial logistic regression, we evaluated the associations between these profiles-and individual parameter changes-and MCI and dementia risk at follow-up.

Results: Of 733 participants (mean age 82.5 ± 2.9 years), 164 (22.4%) developed MCI and 93 (12.7%) developed dementia by the follow-up visit. We identified 3 sleep-wake change profiles: stable sleep (SS; n = 321 [43.8%]) was characterized by stability or small improvements; declining nighttime sleep (n = 256 [34.9%]) showed decreases in nighttime sleep quality and duration, moderate napping increases, and worsening circadian RARs; and increasing sleepiness (IS; n = 156 [21.3%]) exhibited large increases in daytime and nighttime sleep duration and quality, and worsening circadian RARs. After adjustment for age, education, race, body mass index, diabetes, hypertension, myocardial infarction, antidepressant use, and baseline cognition, women with IS had approximately double the risk of dementia (odds ratio 2.21, 95% CI 1.14-4.26) compared with those with SS. SE, WASO, nap duration, and nap frequency were individually associated with dementia. Neither sleep-wake change profiles nor individual parameters were associated with MCI.

Discussion: Among community-dwelling women in their 80s, those with increasing 24-hour sleepiness over 5 years had doubled dementia risk during that time. Change in multidimensional 24-hour sleep-wake activity may serve as an early marker or risk factor for dementia in oldest old women.

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老年妇女24小时睡眠-觉醒活动与痴呆风险的5年变化
背景与目的:睡眠中断与老年人认知老化有关。然而,人们对老年人的纵向睡眠变化以及这些变化是否与认知障碍有关知之甚少。我们的目的是确定24小时多维睡眠-觉醒活动的变化是否与老年妇女轻度认知障碍(MCI)和痴呆有关。方法:我们研究了参加骨质疏松性骨折研究的认知功能正常的女性,她们完成了两次手腕活动摄影(基线和随访),并在随访时使用神经心理学电池和评判评估认知状态。为了确定多维睡眠-觉醒变化概况,我们对夜间睡眠(睡眠持续时间、睡眠效率[SE]和睡眠后觉醒[WASO])、午睡(持续时间和频率)和昼夜休息-活动节律(RARs;峰相,振幅,中间值和稳健性)。使用多项逻辑回归,我们评估了这些特征和个体参数变化与随访时MCI和痴呆风险之间的关系。结果:733名参与者(平均年龄82.5±2.9岁),随访时164名(22.4%)发展为轻度认知障碍,93名(12.7%)发展为痴呆。我们确定了3种睡眠-觉醒变化特征:稳定睡眠(SS);N = 321[43.8%])的特点是稳定或小幅改善;夜间睡眠减少(n = 256[34.9%])表现为夜间睡眠质量和持续时间下降,午睡时间中度增加,昼夜节律RARs恶化;嗜睡增加(IS;n = 156[21.3%])表现出白天和夜间睡眠时间和质量的大幅增加,以及昼夜节律RARs的恶化。在调整了年龄、受教育程度、种族、体重指数、糖尿病、高血压、心肌梗死、抗抑郁药使用和基线认知等因素后,IS女性患痴呆的风险大约是SS女性的两倍(优势比2.21,95% CI 1.14-4.26)。SE、WASO、午睡时间和午睡频率分别与痴呆相关。睡眠-觉醒变化谱和个体参数都与轻度认知损伤无关。讨论:在80多岁的社区妇女中,那些在5年内24小时嗜睡增加的人在此期间患痴呆症的风险增加了一倍。多维24小时睡眠-觉醒活动的变化可能是老年妇女痴呆症的早期标志或风险因素。
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来源期刊
Neurology
Neurology 医学-临床神经学
CiteScore
12.20
自引率
4.00%
发文量
1973
审稿时长
2-3 weeks
期刊介绍: Neurology, the official journal of the American Academy of Neurology, aspires to be the premier peer-reviewed journal for clinical neurology research. Its mission is to publish exceptional peer-reviewed original research articles, editorials, and reviews to improve patient care, education, clinical research, and professionalism in neurology. As the leading clinical neurology journal worldwide, Neurology targets physicians specializing in nervous system diseases and conditions. It aims to advance the field by presenting new basic and clinical research that influences neurological practice. The journal is a leading source of cutting-edge, peer-reviewed information for the neurology community worldwide. Editorial content includes Research, Clinical/Scientific Notes, Views, Historical Neurology, NeuroImages, Humanities, Letters, and position papers from the American Academy of Neurology. The online version is considered the definitive version, encompassing all available content. Neurology is indexed in prestigious databases such as MEDLINE/PubMed, Embase, Scopus, Biological Abstracts®, PsycINFO®, Current Contents®, Web of Science®, CrossRef, and Google Scholar.
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