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Detection of myasthenia gravis using electrooculography signals

机译:使用眼电信号检测重症肌无力

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Myasthenia gravis (MG) is an autoimmune neuromuscular disorder resulting from skeletal muscle weakness and fatigue. An early common symptom is fatigable weakness of the extrinsic ocular muscles; if symptoms remain confined to the ocular muscles after a few years, this is classified as ocular myasthenia gravis (OMG). Diagnosis of MG when there are mild, isolated ocular symptoms can be difficult, and currently available diagnostic techniques are insensitive, non-specific or technically cumbersome. In addition, there are no accurate biomarkers to follow severity of ocular dysfunction in MG over time. Single-fiber electromyography (SFEMG) and repetitive nerve stimulation (RNS) offers a way of detecting and measuring ocular muscle dysfunction in MG, however, challenges of these methods include a poor signal to noise ratio in quantifying eye muscle weakness especially in mild cases. This paper presents one of the attempts to use the electric potentials from the eyes or electrooculography (EOG) signals but obtained from three different forms of sleep testing to differentiate MG patients from age- and gender-matched controls. We analyzed 8 MG patients and 8 control patients and demonstrated a difference in the average eye movements detected between the groups. A classification accuracy as high as 68.8% was achieved using a linear discriminant analysis based classifier.
机译:重症肌无力(MG)是由骨骼肌无力和疲劳引起的一种自身免疫性神经肌肉疾病。早期的常见症状是外在眼肌的可察觉的无力。如果几年后症状仍仅限于眼肌,则可归为重症肌无力(OMG)。当有轻度,孤立的眼部症状时,MG的诊断可能很困难,并且当前可用的诊断技术不灵敏,非特异性或技术上繁琐。此外,尚无准确的生物标志物可随时间追踪MG眼功能障碍的严重程度。单纤维肌电图(SFEMG)和重复性神经刺激(RNS)提供了一种检测和测量MG中眼肌功能障碍的方法,但是,这些方法的挑战包括在量化眼肌无力时信噪比很差,尤其是在轻度情况下。本文提出了一种尝试,利用眼电图或眼电图(EOG)信号的电势,但是从三种不同形式的睡眠测试中获得的,以区分MG患者与年龄和性别匹配的对照组。我们分析了8名MG患者和8名对照患者,并证明了两组之间平均眼动的差异。使用基于线性判别分析的分类器,分类精度高达68.8%。

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