Brain activity in an end-stage ALS patient suggests the presence of an unresponsive wakefulness syndrome.

IF 2.8
Sandra Frycz, Wiktor Więcławski, Marcin Skotniczny, Marek Binder
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Abstract

Objective: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease primarily affecting motor neurons. It is widely assumed that cortical structures beyond motor neurons are relatively preserved, and patients in the end-stage ALS are regarded as being in complete locked-in syndrome (cLIS). However, emerging evidence suggests substantial heterogeneity in cognitive functioning among ALS patients, indicating possible extra-motor cortical involvement and impaired levels of consciousness. We report a case study assessing electrophysiological markers and auditory system integrity to evaluate the presence of covert consciousness in end-stage ALS.

Methods: The patient was a 42-year-old woman with bulbar-onset, end-stage ALS, a six-year disease duration, and no means of communication. She underwent several EEG-based protocols, including resting-state EEG (RS-EEG), a passive auditory oddball paradigm, and 40 Hz auditory steady-state responses (ASSR). Audiological evaluation comprised transient-evoked and distortion-product otoacoustic emissions, as well as auditory brainstem responses (ABR).

Results: RS-EEG was dominated by prefrontal 1-3 Hz activity resembling frontal intermittent rhythmic delta activity. Power spectra were poorly differentiated and consistent with a 1/f profile. No event-related potentials were observed in the oddball paradigm, and no ASSR responses were detected. Audiological testing revealed absent otoacoustic emissions and ABR indicating severe to profound hearing loss.

Conclusions: Our findings indicate severe cortical dysfunction and provide no electrophysiological evidence of covert consciousness. The electrophysiological profile closely resembles that observed in unresponsive wakefulness syndrome. This case supports the hypothesis that advanced ALS following cLIS onset may be more appropriately conceptualized as a disorder of consciousness rather than persistent cLIS.

终末期肌萎缩侧索硬化症患者的脑活动表明存在无反应性觉醒综合征。
目的:肌萎缩性侧索硬化症(ALS)是一种主要影响运动神经元的进行性神经退行性疾病。人们普遍认为,运动神经元以外的皮质结构相对保存,终末期ALS患者被认为处于完全闭锁综合征(cLIS)。然而,新出现的证据表明,ALS患者的认知功能存在实质性的异质性,表明可能存在运动外皮层受累和意识水平受损。我们报告了一个案例研究,评估电生理标志物和听觉系统完整性,以评估终末期ALS中隐蔽意识的存在。方法:患者为一名42岁女性,终末期ALS,球起病,病程6年,无通讯手段。她接受了几种基于脑电图的方案,包括静息状态脑电图(RS-EEG),被动听觉怪异范式和40 Hz听觉稳态反应(ASSR)。听力学评估包括瞬态诱发和畸变产物耳声发射,以及听觉脑干反应(ABR)。结果:RS-EEG以前额叶1 ~ 3hz活动为主,类似于前额叶间歇性节律性δ活动。功率谱分化较差,符合1/f剖面。在odd - ball范式中未观察到事件相关电位,也未检测到ASSR反应。听力学测试显示没有耳声发射和ABR,表明严重到深度听力损失。结论:我们的发现表明严重的皮质功能障碍,并没有提供隐蔽意识的电生理证据。电生理特征与无反应性清醒综合征的电生理特征非常相似。本病例支持以下假设,即cLIS发病后的晚期肌萎缩侧索硬化症可能更适合被定义为一种意识障碍,而不是持续性cLIS。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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