Sleep Disorder Research Center, Department of Medical Science and Public Health, University of Cagliari, Cagliari, Italy.
Nuclear Medicine Unit, Department of Medical Science and Public Health, University of Cagliari, Cagliari, Italy.
Sleep. 2019 Sep 6;42(9). doi: 10.1093/sleep/zsz128.
The neurophysiological hallmark of REM sleep behavior disorder (RBD) is loss of atonia during REM sleep. Indeed, signs and symptoms of neurodegeneration can occur after years, even decades, from its beginning. This study aimed to measure neurophysiological alterations of the brainstem that potentially correlate with the severity of atonia loss, and determining whether a prodromal neurodegenerative disorder underlines this condition when it occurs as an isolated condition (iRBD).
Subjects with iRBD and matched healthy controls were recruited. The study included the recording of one-night polysomnography, vestibular-evoked myogenic potentials (VEMPs), and a [123I]-FP-CIT dopamine transporter (DAT) scan. The quantification of REM sleep without atonia (RSWA) was made according to two previously published manual methods and one automated method.
The rate of alteration of VEMPs and VEMP score were significantly higher in iRBD patients than controls. Moreover, VEMP score was negatively correlated with the automated REM atonia index; a marginal statistical significance was also reached for the positive correlation with the visual tonic electromyographic parameter, while the other correlations, including that with DAT-scan score were not statistically significant.
Brainstem neurophysiology in iRBD can be assessed by VEMPs and their alterations may possibly indicate an early expression of the neurodegenerative process underlying this disorder at the brainstem level, which awaits future longitudinal confirmation. The correlation between RSWA and VEMP alteration might also represent a prodromal aspect anticipating the possible evolution from iRBD to neurodegeneration, whereas DAT-scan abnormalities might represent a later step in this evolution.
快速眼动睡眠行为障碍(RBD)的神经生理学标志是 REM 睡眠期间的去弛缓。事实上,在疾病开始后的数年甚至数十年,神经退行性变的迹象和症状都可能出现。本研究旨在测量脑干的神经生理改变,这些改变可能与去弛缓丧失的严重程度相关,并确定在孤立性 RBD 中是否存在前驱神经退行性疾病。
招募了孤立性 RBD 患者和匹配的健康对照组。该研究包括一夜多导睡眠图、前庭诱发肌源性电位(VEMP)和 [123I]-FP-CIT 多巴胺转运体(DAT)扫描。根据两种以前发表的手动方法和一种自动方法,对 REM 睡眠无弛缓(RSWA)进行了定量。
iRBD 患者的 VEMP 改变率和 VEMP 评分明显高于对照组。此外,VEMP 评分与自动 REM 弛缓指数呈负相关;与视觉紧张性肌电图参数呈正相关,具有边缘统计学意义,而与 DAT 扫描评分的其他相关性则无统计学意义。
孤立性 RBD 的脑干神经生理学可以通过 VEMP 来评估,其改变可能表明该疾病在脑干水平上潜在的神经退行性过程的早期表达,这有待未来的纵向确认。RSWA 与 VEMP 改变之间的相关性也可能代表着向可能从 iRBD 发展为神经退行性变的前驱方面,而 DAT 扫描异常可能代表着这一演变的后期阶段。