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Sleep disturbances and later cognitive status: a multi-centre study.睡眠障碍与后期认知状况:一项多中心研究。
Sleep Med. 2018 Dec;52:26-33. doi: 10.1016/j.sleep.2017.11.1149. Epub 2018 Jan 3.
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Excessive daytime sleepiness may be associated with caudate denervation in Parkinson disease.日间过度嗜睡可能与帕金森病的尾状核去神经支配有关。
J Neurol Sci. 2018 Apr 15;387:220-227. doi: 10.1016/j.jns.2018.02.032. Epub 2018 Feb 21.
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Increased dopaminergic function in the thalamus is associated with excessive daytime sleepiness.丘脑多巴胺能功能的增加与日间过度嗜睡有关。
Sleep Med. 2018 Mar;43:25-30. doi: 10.1016/j.sleep.2017.11.1137. Epub 2017 Dec 12.
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Time-Restricted Feeding Improves Circadian Dysfunction as well as Motor Symptoms in the Q175 Mouse Model of Huntington's Disease.限时喂养可改善亨廷顿病 Q175 小鼠模型的昼夜节律功能障碍和运动症状。
eNeuro. 2018 Jan 3;5(1). doi: 10.1523/ENEURO.0431-17.2017. eCollection 2018 Jan-Feb.
5
Hyposmia Is Associated with RBD for PD Patients with Variants of .嗅觉减退与患有[具体基因名称]变体的帕金森病患者的快速眼动睡眠行为障碍相关。 (注:原文中“with Variants of.”后面缺少具体内容)
Front Aging Neurosci. 2017 Sep 20;9:303. doi: 10.3389/fnagi.2017.00303. eCollection 2017.
6
Slow wave sleep disruption increases cerebrospinal fluid amyloid-β levels.慢波睡眠中断会增加脑脊液中β淀粉样蛋白的水平。
Brain. 2017 Aug 1;140(8):2104-2111. doi: 10.1093/brain/awx148.
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CLOCK rs1801260 Polymorphism is Associated with Susceptibility to Parkinson's Disease in a Chinese Population.CLOCK基因rs1801260多态性与中国人群帕金森病易感性相关。
Neurosci Bull. 2017 Dec;33(6):734-736. doi: 10.1007/s12264-017-0167-5. Epub 2017 Aug 5.
8
Assessment of neuroinflammation in patients with idiopathic rapid-eye-movement sleep behaviour disorder: a case-control study.特发性快速眼动睡眠行为障碍患者的神经炎症评估:病例对照研究。
Lancet Neurol. 2017 Oct;16(10):789-796. doi: 10.1016/S1474-4422(17)30173-4. Epub 2017 Jul 3.
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Sleep Loss Promotes Astrocytic Phagocytosis and Microglial Activation in Mouse Cerebral Cortex.睡眠剥夺促进小鼠大脑皮质中星形胶质细胞的吞噬作用和小胶质细胞的激活。
J Neurosci. 2017 May 24;37(21):5263-5273. doi: 10.1523/JNEUROSCI.3981-16.2017.
10
Effects of circadian clock genes and environmental factors on cognitive aging in old adults in a Taiwanese population.昼夜节律时钟基因和环境因素对台湾老年人群认知衰老的影响。
Oncotarget. 2017 Apr 11;8(15):24088-24098. doi: 10.18632/oncotarget.15493.

帕金森病中的日间过度嗜睡和快速眼动睡眠行为障碍:关于早期干预及其对神经保护意义的叙述性综述

Excessive Daytime Sleepiness and REM Sleep Behavior Disorders in Parkinson's Disease: A Narrative Review on Early Intervention With Implications to Neuroprotection.

作者信息

Gjerstad Michaela D, Alves Guido, Maple-Grødem Jodi

机构信息

The Norwegian Centre for Movement Disorders, Stavanger University Hospital, Stavanger, Norway.

Department of Chemistry, Bioscience and Environmental Engineering, University of Stavanger, Stavanger, Norway.

出版信息

Front Neurol. 2018 Nov 14;9:961. doi: 10.3389/fneur.2018.00961. eCollection 2018.

DOI:10.3389/fneur.2018.00961
PMID:30487775
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6246656/
Abstract

Sleep contributes to the consolidation of our memory and facilitates learning. Short term sleep deprivation temporarily reduces mnestic capacity, whereas long lasting sleep deprivation is associated with structural changes in the hippocampus and cortical areas. However, it is unknown whether early intervention and treatment of sleep disorders could have a neuroprotective effect. In neurodegenerative diseases sleep disorders can occur at preclinical stages and are frequently observed in patients with established Parkinson's disease (PD) and other α-synucleinopathies. REM sleep behavior disorder (RBD) is recognized as a hallmark for the development of α-synucleinopathies and may predict early cognitive decline, while excessive daytime sleepiness (EDS) is present in 12% of patients with PD before treatment initiation and increases continuously over time, causing substantial restrictions for the patients' social life. In more advanced disease, EDS is associated with dementia. Even though well recognized, limited attention has been given to genetics or the treatment of RBD and EDS in early PD. Systematic screening and early intervention can be expected to increase the patients' quality of life, but it remains unclear if this will also impact disease progression. Intervention studies in preclinical and early stages of α-synucleinopathies are needed to increase our understanding of the underlying pathomechanisms and may also provide important inroads to help clarify whether sleep disturbances are secondary to the neurodegenerative process or also contribute to disease exacerbation.

摘要

睡眠有助于巩固我们的记忆并促进学习。短期睡眠剥夺会暂时降低记忆能力,而长期睡眠剥夺与海马体和皮质区域的结构变化有关。然而,睡眠障碍的早期干预和治疗是否具有神经保护作用尚不清楚。在神经退行性疾病中,睡眠障碍可发生在临床前期,并且在已确诊的帕金森病(PD)和其他α-突触核蛋白病患者中经常观察到。快速眼动睡眠行为障碍(RBD)被认为是α-突触核蛋白病发展的一个标志,可能预示早期认知能力下降,而日间过度嗜睡(EDS)在12%的未经治疗的PD患者中存在,并且随时间持续增加,给患者的社交生活带来很大限制。在疾病更晚期,EDS与痴呆有关。尽管已得到充分认识,但在早期PD中,对RBD和EDS的遗传学或治疗关注有限。系统筛查和早期干预有望提高患者的生活质量,但尚不清楚这是否也会影响疾病进展。需要对α-突触核蛋白病的临床前期和早期阶段进行干预研究,以增进我们对潜在病理机制的理解,也可能为帮助阐明睡眠障碍是神经退行性过程的继发结果还是也会导致疾病恶化提供重要切入点。