共核细胞病
快速眼动睡眠行为障碍
医学
前驱期
快速眼动睡眠
睡眠(系统调用)
路易体
疾病
神经科学
帕金森病
α-突触核蛋白
路易氏体型失智症
脑电图
内科学
认知障碍
心理学
痴呆
精神科
操作系统
计算机科学
作者
Johnson D. Pounders,Stuart J. McCarter
出处
期刊:Seminars in Neurology
[Thieme Medical Publishers (Germany)]
日期:2025-03-17
卷期号:45 (03): 348-357
被引量:2
摘要
α-synucleinopathies are a complex group of progressive neurodegenerative disorders with an increasingly recognized long prodromal period, during which sleep dysfunction is a hallmark. Sleep disorders during the prodromal synucleinopathy period, primarily isolated rapid eye movement (REM) sleep behavior disorder (iRBD) and daytime hypersomnolence correlate best with the recently proposed "body-first" Lewy body disease progression. iRBD is the most widely recognized form of prodromal α-synucleinopathy, and patients with iRBD show abnormal α-synuclein in tissues and biofluids even in the absence of cognitive or motor symptoms. More importantly, individuals with iRBD have an elevated risk for near-term development of a clinically diagnosable symptomatic synucleinopathy. Other sleep disorders such as hypersomnia and circadian rhythm dysfunction also occur across the synucleinopathy spectrum, although their prognostic significance is less well understood than iRBD. Finally, isolated REM sleep without atonia may represent an even earlier stage of prodromal synucleinopathy, but further studies are needed.
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