Associations between sleep quality, plasma neurofilament light, and cognition in older adults without dementia.

IF 6.2 1区 医学 Q1 PSYCHIATRY
Hai-Hua Guo, Dong-Xin Liang, Qun Zhang, Yan Fu, Liang-Yu Huang, Ze-Hu Sheng, Lan Tan, Zuo-Teng Wang
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引用次数: 0

Abstract

The relationship between sleep quality, neurofilament light chain (NFL), and cognitive impairment, including the potential effect of plasma NFL in this association, remains unclear. Using the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort, we excluded individuals with dementia or a history of sleep-related medication use at baseline, including 640 participants with complete sleep assessments and covariates. Sleep quality was assessed using the Neuropsychiatric Inventory sleep subscale, which includes ratings of frequency, severity, and their product, with higher scores indicating poorer sleep quality. Baseline and follow-up demographics, sleep indices, plasma NFL levels, and cognition scores (including Mini-Mental State Examination [MMSE], Montreal Cognitive Assessment [MoCA], Alzheimer's Disease Assessment Scale-Cognitive Subscale [ADAS13], Clinical Dementia Rating Scale-Sum of Boxes [CDRSB], Executive Function [EF], Language [LAN], and Memory [MEM]) were also collected. Multivariable linear regression examined the associations between baseline sleep quality, plasma NFL, and cognition, as well as the relationship between sleep quality and longitudinal cognitive decline, calculated using linear mixed-effects models. Mediation analysis evaluated the role of plasma NFL in the sleep-cognition association. Multiple testing significance was corrected using false discovery rate, with results presented as Q-values. Poor sleep quality scores were associated with elevated plasma NFL levels (β: 0.055 to 2.645, P < 0.05), poorer cognition (ADAS13, CDRSB, EF, LAN, MEM; β: -0.188 to 1.279, Q < 0.05), and accelerated longitudinal cognitive decline (MoCA; β: -0.005, Q < 0.05) in both models, with sensitivity analyses supporting these findings. Furthermore, plasma NFL levels partially mediated the relationship between sleep quality and both baseline cognition (ADAS13, CDRSB, LAN, MEM; P < 0.05) and longitudinal cognitive decline (MoCA; P < 0.05), with mediation proportions ranging from 9.2% to 26.7%. Poorer sleep quality was associated with cognitive impairment and accelerated cognitive decline, suggesting its potential role in Alzheimer's disease. These associations may be partially mediated by neuroaxonal injury.

无痴呆老年人睡眠质量、血浆神经丝光和认知之间的关系。
睡眠质量、神经丝轻链(NFL)和认知障碍之间的关系,包括血浆NFL在这种关联中的潜在作用,目前尚不清楚。使用阿尔茨海默病神经影像学倡议(ADNI)队列,我们在基线时排除了患有痴呆症或睡眠相关药物使用史的个体,包括640名具有完整睡眠评估和协变量的参与者。睡眠质量是用神经精神量表睡眠量表来评估的,其中包括频率、严重程度及其产品的评分,得分越高表明睡眠质量越差。还收集了基线和随访人口统计学、睡眠指数、血浆NFL水平和认知评分(包括迷你精神状态检查[MMSE]、蒙特利尔认知评估[MoCA]、阿尔茨海默病评估量表-认知亚量表[ADAS13]、临床痴呆评定量表-盒和量表[CDRSB]、执行功能[EF]、语言[LAN]和记忆[MEM])。多变量线性回归检验了基线睡眠质量、血浆NFL和认知之间的关系,以及睡眠质量和纵向认知能力下降之间的关系,使用线性混合效应模型计算。中介分析评估血浆NFL在睡眠-认知关联中的作用。使用错误发现率校正多重检验显著性,结果以q值表示。睡眠质量评分差与血浆NFL水平升高相关(β: 0.055 ~ 2.645, P
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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