Rapid Eye Movements (REMs) during Non-REM Sleep as a Marker of Alpha-Synucleinopathies.

IF 7.4 1区 医学 Q1 CLINICAL NEUROLOGY
Estefania Vargas Gonzalez,Zhongmei Yang,Pauline Dodet,Smaranda Leu-Semenescu,Andreas Brink-Kjaer,Paul Roujansky,Poul Joergen Jennum,François-Xavier Lejeune,Marie Vidailhet,Isabelle Arnulf
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Abstract

BACKGROUND Alpha-synuclein-related neurodegeneration affects sleep figures, whether in the prodromal (rapid eye movement [REM] sleep behavior disorder, iRBD) or established (Parkinson's disease [PD] and multiple system atrophy [MSA]) stages. OBJECTIVE To look for abnormal intrusions of REMs in non-REM sleep in alpha-synucleinopathies. METHODS Clinical measures and polysomnography were collected from 554 participants with PD (N = 257), iRBD (N = 110), and MSA (N = 71) and 115 controls. Initially, the polysomnography was visually examined for REMs in N2 (presence and index). Subsequently, REMs were automatically detected in all wake and sleep stages, and thresholds discriminating between the disorders were sought. RESULTS The REMs index in N2 (visually measured) was lower in controls than all patients groups. The REMs index in N2 (automatically measured) was lower in controls than in patients with PD and MSA, but not different from iRBD participants. The optimal cutoff of 4.6 REMs/h of N2 yielded a 77% specificity to discriminate controls from all neurodegenerative groups but sensitivity was 60%. The cutoff to discriminate MSA from PD participants had a low specificity (58%). The optimal cutoff of 2.1/h in iRBD patients had an 80% specificity for distinguishing them from controls. CONCLUSIONS Abnormal intrusion of REMs into non-REM sleep distinguishes participants with alpha-synucleinopathies from controls. This automated technique could be used to identify patients with neurodegenerative disorders in the large number of polysomnograms obtained for other purposes in the elderly. © 2025 International Parkinson and Movement Disorder Society.
非快速眼动睡眠期间的快速眼动(rem)作为α -突触核蛋白病的标志。
背景:突触核蛋白相关神经退行性变影响睡眠数据,无论是前驱期(快速眼动[REM]睡眠行为障碍,iRBD)还是成熟期(帕金森病[PD]和多系统萎缩[MSA])。目的观察α -突触核蛋白病患者非快速眼动睡眠时rem的异常侵入。方法收集554例PD患者(257例)、iRBD患者(110例)、MSA患者(71例)和115例对照患者的临床测量数据和多导睡眠图。最初,用多导睡眠图目测N2期的rem(存在和指数)。随后,在所有清醒和睡眠阶段自动检测rem,并寻求区分障碍的阈值。结果对照组N2期REMs指数(目测)均低于各患者组。对照组的N2期REMs指数(自动测量)低于PD和MSA患者,但与iRBD参与者没有差异。4.6 REMs/h的N2的最佳临界值产生了77%的特异性来区分所有神经退行性组的对照组,但敏感性为60%。区分MSA和PD的临界值特异性较低(58%)。在iRBD患者中,2.1/h的最佳临界值具有80%的特异性,可将其与对照组区分开来。结论快速眼动异常侵入非快速眼动睡眠是α -突触核蛋白病患者与对照组的区别。这种自动化技术可用于识别神经退行性疾病患者在大量的多导睡眠图为其他目的获得的老年人。©2025国际帕金森和运动障碍学会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Movement Disorders
Movement Disorders 医学-临床神经学
CiteScore
13.30
自引率
8.10%
发文量
371
审稿时长
12 months
期刊介绍: Movement Disorders publishes a variety of content types including Reviews, Viewpoints, Full Length Articles, Historical Reports, Brief Reports, and Letters. The journal considers original manuscripts on topics related to the diagnosis, therapeutics, pharmacology, biochemistry, physiology, etiology, genetics, and epidemiology of movement disorders. Appropriate topics include Parkinsonism, Chorea, Tremors, Dystonia, Myoclonus, Tics, Tardive Dyskinesia, Spasticity, and Ataxia.
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