Guo Xintong, Liu Xiaoxuan, Ye Shan, Liu Xiangyi, Yang Xu, Fan Dongsheng
Department of Neurology, Peking University Third Hospital, Beijing 100191, China.
Beijing Municipal Key Laboratory of Biomarker and Translational Research in Neurodegenerative Diseases, Beijing 100191, China.
Brain Sci. 2022 Apr 11;12(4):489. doi: 10.3390/brainsci12040489.
It is generally believed that eye movements are completely spared in amyotrophic lateral sclerosis (ALS). Although a series of eye movement abnormalities has been recognized in recent years, the findings are highly controversial, and bulbar disabilities should be considered in relation to eye movement abnormalities. The present study aimed to determine whether eye movement abnormalities are present in ALS and, if so, to investigate their characteristics and their association with bulbar disability in ALS patients. A total of 60 patients and 30 controls were recruited and underwent the standardized evaluations of the oculomotor system using videonystagmography. Square-wave jerks (OR: 16.20, 95% CI: 3.50−74.95, p < 0.001) and abnormal cogwheeling during smooth pursuit (OR: 14.04, 95% CI: 3.00−65.75, p = 0.001) were more frequently observed in ALS patients than in the control subjects. In subgroup analyses, square-wave jerks (OR: 26.51, 95% CI: 2.83−248.05, p = 0.004) and abnormal cogwheeling during smooth pursuit (OR: 6.56, 95% CI: 1.19−36.16, p = 0.031) were found to be more common in ALS patients with bulbar involvement (n = 44) than in those without bulbar involvement (n = 16). There were no significant differences in the investigated eye movement parameters between bulbar-onset (n = 12) and spinal-onset patients (n = 48). ALS patients showed a range of eye movement abnormalities, affecting mainly the ocular fixation and smooth pursuit systems. Our pioneering study indicates that the region of involvement could better indicate the pathophysiological essence of the abnormalities than the type of onset pattern in ALS. Eye movement abnormalities may be potential clinical markers for objectively evaluating upper brainstem or supratentorial cerebral lesion neurodegeneration in ALS.
一般认为,肌萎缩侧索硬化症(ALS)患者的眼球运动完全不受影响。尽管近年来已认识到一系列眼球运动异常情况,但这些发现极具争议性,并且应结合眼球运动异常来考虑延髓功能障碍。本研究旨在确定ALS患者是否存在眼球运动异常,若存在,则调查其特征以及与ALS患者延髓功能障碍的关联。共招募了60例患者和30名对照者,并使用视频眼震图对动眼系统进行标准化评估。与对照者相比,ALS患者更频繁地出现方波急跳(比值比:16.20,95%置信区间:3.50 - 74.95,p < 0.001)和平滑跟踪时的异常齿轮样现象(比值比:14.04,95%置信区间:3.00 - 65.75,p = 0.001)。在亚组分析中,发现方波急跳(比值比:26.51,95%置信区间:2.83 - 248.05,p = 0.004)和平滑跟踪时的异常齿轮样现象(比值比:6.56,95%置信区间:1.19 - 36.16,p = 0.031)在有延髓受累的ALS患者(n = 44)中比无延髓受累的患者(n = 16)更常见。延髓起病(n = 12)和脊髓起病患者(n = 48)之间在研究的眼球运动参数上无显著差异。ALS患者表现出一系列眼球运动异常,主要影响眼球注视和平滑跟踪系统。我们的开创性研究表明,受累区域比ALS的起病模式类型更能准确反映异常的病理生理本质。眼球运动异常可能是客观评估ALS患者上脑干或幕上脑病变神经变性的潜在临床标志物。