嗜睡
共核细胞病
快速眼动睡眠行为障碍
非快速眼动睡眠
路易氏体型失智症
快速眼动睡眠
医学
痴呆
心理学
神经科学
疾病
多导睡眠图
眼球运动
帕金森病
内科学
脑电图
α-突触核蛋白
作者
Yves Dauvilliers,Carlos H. Schenck,Ronald B. Postuma,Álex Iranzo,Pierre‐Hervé Luppi,Giuseppe Plazzi,Jacques Montplaisir,Bradley F. Boeve
标识
DOI:10.1038/s41572-018-0016-5
摘要
Rapid eye movement (REM) sleep behaviour disorder (RBD) is a parasomnia that is characterized by loss of muscle atonia during REM sleep (known as REM sleep without atonia, or RSWA) and abnormal behaviours occurring during REM sleep, often as dream enactments that can cause injury. RBD is categorized as either idiopathic RBD or symptomatic (also known as secondary) RBD; the latter is associated with antidepressant use or with neurological diseases, especially α-synucleinopathies (such as Parkinson disease, dementia with Lewy bodies and multiple system atrophy) but also narcolepsy type 1. A clinical history of dream enactment or complex motor behaviours together with the presence of muscle activity during REM sleep confirmed by video polysomnography are mandatory for a definite RBD diagnosis. Management involves clonazepam and/or melatonin and counselling and aims to suppress unpleasant dreams and behaviours and improve bedpartner quality of life. RSWA and RBD are now recognized as manifestations of an α-synucleinopathy; most older adults with idiopathic RBD will eventually develop an overt neurodegenerative syndrome. In the future, studies will likely evaluate neuroprotective therapies in patients with idiopathic RBD to prevent or delay α-synucleinopathy-related motor and cognitive decline.
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