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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.

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。

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