Department of Neuroscience - Unit of Neurorehabilitation, IRCCS Bambino Gesù Children's Hospital, Rome - Via Torre Di Palidoro s.n.c. 00050, Palidoro, Rome, Italy.
Department of Neuroscience - Unit of Neurorehabilitation, IRCCS Bambino Gesù Children's Hospital, Rome - Via Torre Di Palidoro s.n.c. 00050, Palidoro, Rome, Italy; Department of Neuroscience - Unit of Neuromuscolar and Neurodegenerative Diseases, IRCCS Bambino Gesù Children's Hospital, Rome - Piazza Di Sant'Onofrio 4, 00165, Rome, Italy; Department Systems Medicine, University of Roma Tor Vergata, Rome - Via Montpellier 1, 00133, Rome, Italy.
J Neurosci Methods. 2020 May 15;338:108697. doi: 10.1016/j.jneumeth.2020.108697. Epub 2020 Mar 20.
Friedreich Ataxia (FRDA) and other inherited chronic ataxias (CAs) are common causes of early onset ataxias (EOA), a group of conditions still lacking effective therapies and biomarkers. Ocular saccades are considered a reliable paradigm of motor control, useful to track the functioning of underlying neural networks and serving as potential markers for neurological diseases.
A non-invasive video-oculography device (EyeSeeCam) was used to test saccadic parameters (latency, amplitude, duration, velocity) and peak velocity/amplitude ratio ("main sequence") in pediatric patients with FRDA, CAs and healthy controls, providing correlations with standard clinical scores.
Pattern of saccadic features differed between CA and FRDA. The main sequence analysis was impaired respectively in vertical saccades in CA, and in horizontal saccades in FRDA. In CA, the amplitude of vertical saccades was reduced, and the size inversely correlated with the Scale for the assessment and rating of ataxia (SARA) score. In FRDA the amplitude of horizontal saccades directly correlated with SARA score.
EyeSeeCam allowed testing saccades easily and quickly even in pediatric patients with EOA.
The pattern of saccadic impairment differed between FRDA and CAs, resulting a prominent involvement of vertical saccades in CA and of horizontal ones in FRDA, which respectively correlated with SARA score. Since such differences may reflect distinct pathophysiological substrates, saccades emerged as a potential source of biomarkers in EOAs. Availability of handy tools, such as EyeSeeCam, may facilitate future research in this field.
弗里德里希共济失调(FRDA)和其他遗传性慢性共济失调(CA)是早发性共济失调(EOA)的常见原因,EOA 是一组缺乏有效治疗方法和生物标志物的疾病。眼跳被认为是运动控制的可靠范例,可用于跟踪潜在神经网络的功能,并作为潜在的神经疾病标志物。
使用非侵入性视频眼动描记仪(EyeSeeCam)测试 FRDA、CA 和健康对照组儿科患者的眼跳参数(潜伏期、幅度、持续时间、速度)和峰值速度/幅度比(“主序列”),并与标准临床评分相关。
眼跳特征模式在 CA 和 FRDA 之间存在差异。主序列分析分别在 CA 的垂直眼跳和 FRDA 的水平眼跳中受损。在 CA 中,垂直眼跳幅度减小,大小与共济失调评定量表(SARA)评分呈反比。在 FRDA 中,水平眼跳幅度与 SARA 评分直接相关。
即使在患有 EOA 的儿科患者中,EyeSeeCam 也可以轻松快速地测试眼跳。
FRDA 和 CA 之间的眼跳障碍模式不同,导致 CA 中垂直眼跳明显受累,FRDA 中水平眼跳受累,分别与 SARA 评分相关。由于这些差异可能反映了不同的病理生理基础,因此眼跳成为 EOA 中潜在的生物标志物来源。EyeSeeCam 等便捷工具的可用性可能会促进该领域的未来研究。