Department of Neurology, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bengaluru, India.
Department of Neurophysiology, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bengaluru, India.
Sleep Med. 2018 Feb;42:97-102. doi: 10.1016/j.sleep.2017.09.030. Epub 2017 Oct 25.
Spinocerebellar ataxias are progressive neurodegenerative disorders characterized by progressive cerebellar features with additional neuro-axis involvement. Oculomotor abnormality is one of the most frequent manifestations. This study was done to assess the polysomnographic abnormalities in patients with Spinocerebellar ataxia (SCA1, SCA2 and SCA3) and also to evaluate whether oculomotor abnormalities interfere with sleep stage R scoring.
The study was carried out using 36 genetically positive SCA patients. All patients underwent neurological examination with special focus on oculomotor function (optokinetic nystagmus-OKN and extraocular movement restriction-EOM). The sleep quality was measured with Pittsburgh Sleep Quality Index (PSQI) and Epworth Sleepiness Scale (ESS). Disease severity was assessed with International Cooperative Ataxia Rating Scale (ICARS). All the patients underwent over-night video-polysomnography (VPSG).
Out of 36 patients studied, the data of 34 patients [SCA1 (n = 12), SCA2 (n = 13), SCA3 (n = 9)] were used for final analysis. Patients from SCA1, SCA2, and SCA3 category did not show significant differences in age and diseases severity (ICARS). All patients had vertical OKN impairment. Oculomotor impairment was higher in SCA2 patients. Sleep macro-architecture analysis showed absent stage R sleep, predominantly in SCA2 (69%) followed by SCA3 (44%) and SCA1 (8%). Patients showed a strong negative correlation of stage R sleep percentage with disease severity and oculomotor dysfunction.
Voluntary saccadic eye movement velocity and rapid eye movements (REMs) in sleep are strongly correlated. The more severe the saccadic velocity impairment, the less likely was it to generate REMs (rapid eye movements) during stage R. Accordingly 69% of SCA2 patients with severe occulomotor impairments showed absent stage R as per the AASM sleep scoring. We presume that the impaired REMs generation in sleep could be due to oculomotor abnormality and has resulted in spuriously low or absent stage R sleep percentage in SCA patients with conventional VPSG scoring rules. The present study recommends the modification of AASM scoring rules for stage R in patients with oculomotor abnormalities.
脊髓小脑共济失调是一种进行性神经退行性疾病,其特征是进行性小脑特征,伴有额外的神经轴受累。眼球运动异常是最常见的表现之一。本研究旨在评估脊髓小脑共济失调(SCA1、SCA2 和 SCA3)患者的多导睡眠图异常,并评估眼球运动异常是否会干扰睡眠期 R 评分。
该研究使用了 36 名经基因证实的 SCA 患者。所有患者均接受了神经系统检查,特别关注眼球运动功能(视动性眼球震颤-OKN 和眼外肌运动受限-EOM)。睡眠质量采用匹兹堡睡眠质量指数(PSQI)和 Epworth 嗜睡量表(ESS)进行评估。疾病严重程度采用国际合作共济失调评分量表(ICARS)进行评估。所有患者均接受了夜间视频多导睡眠图(VPSG)检查。
在 36 名研究患者中,34 名患者的数据[ SCA1(n=12)、SCA2(n=13)、SCA3(n=9)]用于最终分析。SCA1、SCA2 和 SCA3 组患者的年龄和疾病严重程度(ICARS)无显著差异。所有患者均存在垂直 OKN 损害。SCA2 患者的眼球运动障碍更严重。睡眠宏观结构分析显示,SCA2(69%)后依次是 SCA3(44%)和 SCA1(8%)患者的 R 期睡眠缺失。患者的 R 期睡眠百分比与疾病严重程度和眼球运动功能呈强烈负相关。
自愿性扫视眼动速度和睡眠中的快速眼动(REMs)呈强相关。扫视速度损伤越严重,R 期产生 REMs(快速眼动)的可能性就越低。因此,根据 AASM 睡眠评分,69%的 SCA2 患者存在严重的眼球运动障碍,其 R 期睡眠缺失。我们推测,睡眠中 REMs 的产生受损可能是由于眼球运动异常所致,这导致了 SCA 患者在常规 VPSG 评分规则下的 R 期睡眠百分比偏低或缺失。本研究建议对存在眼球运动异常的患者的 AASM R 期评分规则进行修改。