GIGA-Cyclotron Research Centre-In Vivo Imaging, University of Liège, Liège, Belgium.
Psychology and Cognitive Neuroscience Research Unit, University of Liège, Liège, Belgium.
Elife. 2022 May 31;11:e78191. doi: 10.7554/eLife.78191.
Sleep alteration is a hallmark of ageing and emerges as a risk factor for Alzheimer's disease (AD). While the fine-tuned coalescence of sleep microstructure elements may influence age-related cognitive trajectories, its association with AD processes is not fully established. Here, we investigated whether the coupling of spindles and slow waves (SW) is associated with early amyloid-β (Aβ) brain burden, a hallmark of AD neuropathology, and cognitive change over 2 years in 100 healthy individuals in late-midlife (50-70 years; 68 women). We found that, in contrast to other sleep metrics, earlier occurrence of spindles on slow-depolarisation SW is associated with higher medial prefrontal cortex Aβ burden (p=0.014, r²=0.06) and is predictive of greater longitudinal memory decline in a large subsample (p=0.032, r²=0.07, N=66). These findings unravel early links between sleep, AD-related processes, and cognition and suggest that altered coupling of sleep microstructure elements, key to its mnesic function, contributes to poorer brain and cognitive trajectories in ageing.
睡眠改变是衰老的一个标志,也是阿尔茨海默病(AD)的一个风险因素。虽然睡眠微结构元素的精细融合可能会影响与年龄相关的认知轨迹,但它与 AD 进程的关系尚未完全确定。在这里,我们研究了纺锤波和慢波(SW)的耦合是否与 AD 神经病理学的早期淀粉样蛋白-β(Aβ)脑负荷以及 100 名中年后期(50-70 岁;68 名女性)健康个体 2 年内的认知变化有关。我们发现,与其他睡眠指标相比,在慢去极化 SW 上更早出现的纺锤波与内侧前额叶皮质 Aβ负荷较高有关(p=0.014,r²=0.06),并且在一个较大的亚组中对纵向记忆下降具有预测性(p=0.032,r²=0.07,N=66)。这些发现揭示了睡眠、AD 相关过程和认知之间的早期联系,并表明睡眠微结构元素耦合的改变,这是其记忆功能的关键,导致衰老过程中大脑和认知轨迹较差。