Nolan Emma, Sun Yunyi, Shi Hui, Archer Derek, Perry Arden, Pechman Kimberly, Shashikumar Niranjana, Landman Bennett, Gogniat Marissa, Liu Dandan, Zhang Panpan, Hohman Timothy J, Jefferson Angela L, Full Kelsie M
Vanderbilt Memory and Alzheimer's Center, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Epidemiology Doctoral Program, School of Medicine, Vanderbilt University, Nashville, Tennessee, USA.
Alzheimers Dement. 2025 Jun;21(6):e70364. doi: 10.1002/alz.70364.
Poor sleep may be a risk factor for neurodegeneration and Alzheimer's disease (AD). Few studies have examined objectively measured sleep with structural neuroimaging measures.
Vanderbilt Memory and Aging Project participants (N = 407; median age: 70 years) wore ActiGraph accelerometers for 10 days to estimate sleep regularity, timing, efficiency, duration, wake-after-sleep onset, and awakening length. Volume in brain regions of interest (ROIs) and AD signatures were quantified using 3T brain magnetic resonance imaging (MRI). Cross-sectional linear regression models were adjusted for sociodemographic and lifestyle factors, depression, cognitive status, and cardiovascular risk. ROI and McEvoy models were adjusted for total intracranial volume.
Greater sleep irregularity (β= -0.12, p = 0.005; β= -0.07, p = 0.024) and longer awakening length (β= -0.11, p = 0.009; β= -0.08, p = 0.012) were associated with smaller volumes in ROIs related to AD.
More irregular and fragmented sleep was associated with smaller volume in ROIs vulnerable to AD, indicating a potential link between poor sleep and neurodegeneration.
Associations between sleep and brain health are poorly understood. Gray matter atrophy by irregular sleep may imply Alzheimer's disease (AD) decline. Increased sleep irregularity is associated with smaller brain region volume. Sleep disruption, estimated by awakening length, is linked to AD-related brain volume.
睡眠不佳可能是神经退行性变和阿尔茨海默病(AD)的一个风险因素。很少有研究使用结构神经影像学测量方法来客观地研究睡眠情况。
范德比尔特记忆与衰老项目的参与者(N = 407;中位年龄:70岁)佩戴ActiGraph加速度计10天,以估计睡眠规律性、时间安排、效率、时长、睡眠后觉醒和觉醒时长。使用3T脑磁共振成像(MRI)对感兴趣脑区(ROI)的体积和AD特征进行量化。横断面线性回归模型针对社会人口统计学和生活方式因素、抑郁、认知状态和心血管风险进行了调整。ROI模型和麦克沃伊模型针对总颅内体积进行了调整。
更高的睡眠不规律性(β = -0.12,p = 0.005;β = -0.07,p = 0.024)和更长的觉醒时长(β = -0.11,p = 0.009;β = -0.08,p = 0.012)与AD相关ROI的较小体积有关。
睡眠更加不规律和碎片化与易患AD的ROI较小体积有关,表明睡眠不佳与神经退行性变之间存在潜在联系。
睡眠与脑健康之间的关联尚不清楚。不规则睡眠导致的灰质萎缩可能意味着阿尔茨海默病(AD)病情恶化。睡眠不规律性增加与脑区体积较小有关。通过觉醒时长估计的睡眠中断与AD相关脑体积有关。