Division of Sleep and Circadian Disorders, Brigham and Women's Hospital, Harvard Medical School, Boston, USA; Division of Neurology, University of British Columbia, Vancouver, Canada.
Division of Neurology, University of British Columbia, Vancouver, Canada; Department of Neurosciences, University of California, San Diego, La Jolla, USA.
Prog Neurobiol. 2021 Feb;197:101902. doi: 10.1016/j.pneurobio.2020.101902. Epub 2020 Aug 30.
A majority of patients with Alzheimer's disease (AD) experience some form of sleep disruption, including nocturnal sleep fragmentation, increased daytime napping, decreased slow-wave sleep (SWS, stage N3), and decreased rapid-eye-movement sleep (REM). Clinical studies are investigating whether such sleep disturbances are a consequence of the underlying disease, and whether they also contribute to the clinical and pathological manifestations of AD. Emerging research has provided a direct link between several of these sleep disruptions and AD pathophysiology, suggesting that treating sleep disorders in this population may target basic mechanisms of the disease. Here, we provide a comprehensive review of sleep disturbances associated with the spectrum of AD, ranging from the preclinical stages through dementia. We discuss how sleep interacts with AD pathophysiology and, critically, whether sleep impairments can be targeted to modify the disease course in a subgroup of affected AD patients. Ultimately, larger studies that fully utilize new diagnostic and experimental tools will be required to better define the most relevant sleep disturbance to target in AD, the interventions that best modulate this target symptom, and whether successful early intervention can modify AD risk and prevent dementia.
大多数阿尔茨海默病(AD)患者都经历某种形式的睡眠障碍,包括夜间睡眠碎片化、白天小睡增加、慢波睡眠(SWS,N3 期)减少和快速眼动睡眠(REM)减少。临床研究正在调查这些睡眠障碍是否是潜在疾病的结果,以及它们是否也导致 AD 的临床和病理表现。新出现的研究为其中一些睡眠障碍与 AD 病理生理学之间的直接联系提供了依据,这表明在该人群中治疗睡眠障碍可能针对疾病的基本机制。在这里,我们全面回顾了与 AD 谱相关的睡眠障碍,从临床前阶段到痴呆。我们讨论了睡眠如何与 AD 病理生理学相互作用,以及睡眠障碍是否可以作为一个亚组 AD 患者疾病进程的靶点。最终,需要更大规模的研究,充分利用新的诊断和实验工具,以更好地确定 AD 中最相关的目标睡眠障碍、最能调节该目标症状的干预措施,以及早期成功干预是否能改变 AD 风险并预防痴呆。