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90 岁以上人群中与 19 至 40 年前睡眠时间相关的神经病理学变化:90+ 研究。

Neuropathologic changes at age 90+ related to sleep duration 19 to 40 years earlier: The 90+ Study.

机构信息

Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, California, USA.

Department of Neurology, University of California, Orange, California, USA.

出版信息

Alzheimers Dement. 2024 May;20(5):3495-3503. doi: 10.1002/alz.13798. Epub 2024 Apr 11.

Abstract

INTRODUCTION

We investigated the association between sleep duration and neuropathologic changes 19 to 40 years later in oldest-old (age 90+) participants of The 90+ Study.

METHODS

Participants self-reported sleep duration and underwent neuropathologic evaluation. We categorized sleep duration as < 7, 7 to 8 = reference, > 8 hours and dichotomized neuropathologic changes as present/absent. We estimated odds ratio (OR) and 95% confidence intervals (CI) using logistic regression.

RESULTS

In 264 participants, mean age at sleep self-report was 69 years, mean age at autopsy was 98 years, and mean interval between sleep self-report and autopsy was 29 years (range: 19-40). Those reporting > 8 hours of sleep had lower likelihood of limbic-predominant age-related TDP-43 encephalopathy neuropathologic change (LATE-NC) inclusions (OR = 0.18; CI = 0.04-0.82) and amyloid beta deposits (OR = 0.34; 95% CI = 0.12-0.94).

DISCUSSION

Long self-reported sleep is associated with lower odds of neurodegenerative neuropathologic changes 19 to 40 years later in the oldest-old, suggesting a potential role of sleep in accumulation of dementia-related neuropathologies.

HIGHLIGHTS

Association of self-reported sleep with non-Alzheimer's disease neuropathologic changes has not been explored. Whether sleep duration is related to dementia neuropathologic changes decades later is unclear. Long self-reported sleep is associated with lower odds of Alzheimer's disease neuropathologic change 19 to 40 years later in the oldest-old. Long self-reported sleep is associated with lower odds of limbic-predominant age-related TDP-43 encephalopathy neuropathologic change 19 to 40 years later in the oldest-old.

摘要

简介

我们研究了睡眠时长与认知症相关神经病理变化之间的关联,这些认知症相关神经病理变化是在年龄最大的(90 岁以上)参与者中 19 至 40 年后通过 The 90+ Study 检测到的。

方法

参与者自我报告了睡眠时长,并接受了神经病理学评估。我们将睡眠时长分为<7 小时、7 至 8 小时(参考值)和>8 小时,并将神经病理变化分为存在/不存在。我们使用逻辑回归估计了比值比(OR)和 95%置信区间(CI)。

结果

在 264 名参与者中,睡眠报告时的平均年龄为 69 岁,尸检时的平均年龄为 98 岁,睡眠报告与尸检之间的平均间隔为 29 年(范围为 19-40 年)。报告睡眠时间>8 小时的参与者,其出现与年龄相关的 tau 蛋白病(TDP-43)为主的神经退行性病变(LATE-NC)包涵体(OR=0.18;95%CI=0.04-0.82)和淀粉样β沉积(OR=0.34;95%CI=0.12-0.94)的可能性较低。

讨论

在年龄最大的老年人中,长期自我报告的睡眠与 19 至 40 年后神经退行性神经病理变化的可能性降低有关,这表明睡眠可能在痴呆相关神经病理的积累中发挥作用。

重点

自我报告的睡眠与非阿尔茨海默病神经病理变化之间的关系尚未得到探索。睡眠时长是否与几十年后痴呆症的神经病理变化有关还不清楚。在年龄最大的老年人中,长期自我报告的睡眠与 19 至 40 年后阿尔茨海默病神经病理变化的可能性降低有关。在年龄最大的老年人中,长期自我报告的睡眠与 19 至 40 年后以边缘系统为主的与年龄相关的 TDP-43 脑病神经病理变化的可能性降低有关。

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