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Degeneration of rapid eye movement sleep circuitry underlies rapid eye movement sleep behavior disorder

机译:快速眼球运动的退化睡眠电路利用快速眼球运动睡眠行为障碍

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ABSTRACT During healthy rapid eye movement sleep, skeletal muscles are actively forced into a state of motor paralysis. However, in rapid eye movement sleep behavior disorder—a relatively common neurological disorder—this natural process is lost. A lack of motor paralysis (atonia) in rapid eye movement sleep behavior disorder allows individuals to actively move, which at times can be excessive and violent. At first glance this may sound harmless, but it is not because rapid eye movement sleep behavior disorder patients frequently injure themselves or the person they sleep with. It is hypothesized that the degeneration or dysfunction of the brain stem circuits that control rapid eye movement sleep paralysis is an underlying cause of rapid eye movement sleep behavior disorder. The link between brain stem degeneration and rapid eye movement sleep behavior disorder stems from the fact that rapid eye movement sleep behavior disorder precedes, in the majority (~80%) of cases, the development of synucleinopathies such as Parkinson's disease, dementia with Lewy bodies, and multiple system atrophy, which are known to initially cause degeneration in the caudal brain stem structures where rapid eye movement sleep circuits are located. Furthermore, basic science and clinical evidence demonstrate that lesions within the rapid eye movement sleep circuits can induce rapid eye movement sleep‐specific motor deficits that are virtually identical to those observed in rapid eye movement sleep behavior disorder. This review examines the evidence that rapid eye movement sleep behavior disorder is caused by synucleinopathic neurodegeneration of the core brain stem circuits that control healthy rapid eye movement sleep and concludes that rapid eye movement sleep behavior disorder is not a separate clinical entity from synucleinopathies but, rather, it is the earliest symptom of these disorders. ? 2017 International Parkinson and Movement Disorder Society
机译:摘要在健康快速眼动睡眠中,骨骼肌积极被迫进入电机瘫痪状态。然而,在快速的眼睛运动睡眠行为障碍 - 一种相对常见的神经疾病 - 这种自然过程丢失。在快速眼球运动睡眠行为障碍中缺乏运动瘫痪(Adonia)允许个人积极移动,有时可能会过度和暴力。乍一看,这可能听起来无害,但它不是因为快速的眼睛运动睡眠行为障碍患者经常伤害自己或他们睡觉的人。假设控制快速眼睛运动睡眠麻痹的脑干电路的变性或功能障碍是快速眼球运动睡眠行为障碍的潜在原因。脑干变性和快速眼球运动睡眠行为障碍的联系源于迅速眼动睡眠行为障碍的事实源自,在大多数(〜80%)的病例中,帕金森病等核苷酸的发展,痴呆症与雄鹿症和多种系统萎缩,已知在尾部运动睡眠电路的尾部脑干结构中最初引起变性。此外,基础科学和临床证据表明,快速眼动睡眠电路内的病变可以诱导快速的眼睛运动睡眠特定的电动机缺陷,这些电机缺陷几乎与快速眼睛运动睡眠行为障碍观察到的那些。本综述审查了快速眼部运动睡眠行为障碍是由控制健康快速眼球运动睡眠的核心视网膜电路的突触核视力神经变性引起的证据,并得出快速眼动睡眠行为障碍并不是来自核苷酸的快速临床实体,而是,这是这些疾病的最早症状。还2017年国际帕金森和运动障碍协会

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