Desel Tenzin, Walker Matthew P, Brown Chelsea, Chen Cindy, Chadwick Trevor A, Jagust William J, Sharon Omer
Center for Human Sleep Science, Department of Psychology, University of California, Berkeley, USA.
Helen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, CA, USA.
bioRxiv. 2025 Aug 22:2025.08.18.670879. doi: 10.1101/2025.08.18.670879.
Rapid Eye Movement (REM) sleep degrades with age, and more severely in Alzheimer's disease (AD). REM sleep comprises about twenty percent of adult sleep, alternates between phasic and tonic periods, and includes delta waves (1-4Hz) in two forms: fast sawtooth waves and slower, NREM-like waves, whose expression dynamically varies across REM periods. Yet, the functional relevance of these REM sleep delta waves remains unknown. Here, using two independent cohorts, we show that aging is associated with a shift from fast sawtooth to slow NREM-like delta waves, particularly during phasic REM sleep-a period typically marked by high cortical activation. Beyond chronological age, this shift is associated with amyloid-beta and tau burden, suggesting that AD pathology disrupts REM-specific oscillatory patterns. Furthermore, this shift in REM oscillations is linked to impaired overnight memory consolidation, independent of NREM sleep quality. Moreover, variation in ApoE alleles, a major genetic risk factor for AD, was independently associated with a reduction in fast sawtooth wave density, thereby linking a genetic predisposition for AD to these specific REM microstructural changes. These findings identify a novel signature of memory decline in aging and implicate REM sleep as a distinct vulnerable substrate through which AD pathology may impair brain function.
快速眼动(REM)睡眠会随着年龄增长而退化,在阿尔茨海默病(AD)中退化更为严重。REM睡眠约占成年人睡眠的20%,在相位期和紧张期之间交替,包括两种形式的δ波(1-4Hz):快速锯齿波和较慢的、类似非快速眼动(NREM)的波,其表现会在REM睡眠期间动态变化。然而,这些REM睡眠δ波的功能相关性仍然未知。在这里,我们使用两个独立的队列研究表明,衰老与从快速锯齿波向类似NREM的慢δ波转变有关,特别是在相位REM睡眠期间——这一时期通常以高皮质激活为特征。除了实际年龄外,这种转变还与淀粉样蛋白β和tau蛋白负荷有关,表明AD病理会破坏REM特异性振荡模式。此外,REM振荡的这种转变与夜间记忆巩固受损有关,且与NREM睡眠质量无关。此外,ApoE等位基因的变异是AD的主要遗传风险因素,它与快速锯齿波密度的降低独立相关,从而将AD的遗传易感性与这些特定的REM微观结构变化联系起来。这些发现确定了衰老过程中记忆衰退的一种新特征,并表明REM睡眠是AD病理可能损害脑功能的一个独特的脆弱底物。