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Non-REM Sleep Characteristics Predict Early Cognitive Impairment in an Aging Population

机译:非快速眼动睡眠特征预测人口老龄化的早期认知障碍

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>Objective: Recent research suggests that sleep disorders or changes in sleep stages or EEG waveform precede over time the onset of the clinical signs of pathological cognitive impairment (e.g., Alzheimer's disease). The aim of this study was to identify biomarkers based on EEG power values and spindle characteristics during sleep that occur in the early stages of mild cognitive impairment (MCI) in older adults.>Methods: This study was a case-control cross-sectional study with 1-year follow-up of cases. Patients with isolated subjective cognitive complaints (SCC) or MCI were recruited in the Bordeaux Memory Clinic (MEMENTO cohort). Cognitively normal controls were recruited. All participants were recorded with two successive polysomnography 1 year apart. Delta, theta, and sigma absolute spectral power and spindle characteristics (frequency, density, and amplitude) were analyzed from purified EEG during NREM and REM sleep periods during the entire second night.>Results: Twenty-nine patients (8 males, age = 71 ± 7 years) and 29 controls were recruited at T0. Logistic regression analyses demonstrated that age-related cognitive impairment were associated with a reduced delta power (odds ratio (OR) 0.072, P < 0.05), theta power (OR 0.018, P < 0.01), sigma power (OR 0.033, P < 0.05), and spindle maximal amplitude (OR 0.002, P < 0.05) during NREM sleep. Variables were adjusted on age, gender, body mass index, educational level, and medication use. Seventeen patients were evaluated at 1-year follow-up. Correlations showed that changes in self-reported sleep complaints, sleep consolidation, and spindle characteristics (spectral power, maximal amplitude, duration, and frequency) were associated with cognitive impairment (P < 0.05).>Conclusion: A reduction in slow-wave, theta and sigma activities, and a modification in spindle characteristics during NREM sleep are associated very early with a greater risk of the occurrence of cognitive impairment. Poor sleep consolidation, lower amplitude, and faster frequency of spindles may be early sleep biomarkers of worsening cognitive decline in older adults.
机译:>目的:最近的研究表明,睡眠障碍或睡眠阶段的变化或EEG波形会随时间推移而提前出现病理性认知障碍(例如阿尔茨海默氏病)的临床体征。这项研究的目的是根据在老年人轻度认知障碍(MCI)早期发生的睡眠中的脑电图功率值和纺锤体特征来识别生物标志物。>方法:对照横断面研究,病例随访一年。患有孤立主观认知障碍(SCC)或MCI的患者被纳入波尔多记忆诊所(MEMENTO队列)。募集认知正常对照。所有参与者都记录了相隔1年的两次连续多导睡眠图。在整个第二夜的NREM和REM睡眠期间,从纯净的EEG分析了Delta,theta和sigma的绝对频谱功率和纺锤特征(频率,密度和振幅)。>结果: 29名患者在T0时招募了8名男性(年龄= 71±7岁)和29名对照。 Logistic回归分析表明,年龄相关的认知障碍与降低的delta功效(优势比(OR)0.072,P <0.05),θ功效(OR 0.018,P <0.01),sigma功效(OR 0.033,P <0.05)相关。 )和NREM睡眠期间的主轴最大振幅(OR 0.002,P <0.05)。根据年龄,性别,体重指数,教育程度和药物使用情况对变量进行调整。在1年的随访中评估了17名患者。相关性表明,自我报告的睡眠抱怨,睡眠巩固和心轴特征(频谱功率,最大振幅,持续时间和频率)的变化与认知障碍相关(P <0.05)。>结论: NREM睡眠期间慢波,theta和sigma活动的减少以及纺锤体特征的改变与早期发生认知障碍的更大风险相关。不良的睡眠巩固,较低的振幅和较快的纺锤体频率可能是老年人认知能力恶化的早期睡眠生物标志。

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