Mordillo-Mateos Laura, Soto-Leon Vanesa, Torres-Pareja Marta, Peinado-Palomino Diego, Mendoza-Laiz Nuria, Alonso-Bonilla Carlos, Dileone Michele, Rotondi Mario, Aguilar Juan, Oliviero Antonio
FENNSI Group, Hospital Nacional de Parapléjicos, Servicio de Salud de Castilla La Mancha, Toledo, Spain.
Facultad de Ciencias del Deporte, University of Castilla La Mancha, Toledo, Spain.
Front Neurol. 2019 Apr 9;10:339. doi: 10.3389/fneur.2019.00339. eCollection 2019.
Multiple sclerosis (MS) is an autoimmune disorder of the CNS in which inflammation, demyelination, and axonal damage of the central nervous system coexist. Fatigue is one of the most disabling symptoms in MS and little is known about the neurophysiological mechanisms involved. To give more mechanistic insight of fatigue in MS, we studied a cohort of 17 MS patients and a group of 16 age-matched healthy controls. Baseline Fatigue Severity Scales and Fatigue Rating were obtained from both groups to check the level of fatigue and to perform statistical correlations with fatigue-induced neurophysiologic changes. To induce fatigue we used a handgrip task. During the fatiguing task, we evaluated fatigue state (using a dynamometer) and after the task we evaluated the Borg Rating of Perceived Exertion Scale. Transcranial magnetic stimulation and peripheral electric stimulation were used to assess corticospinal tract and peripheral system functions before and after the task. Clinically significant fatigue and central motor conduction time were greater in patients than in controls, while motor cortex excitability was decreased and maximal handgrip strength reduced in patients. Interestingly, fatigue state was positively correlated to perceived fatigue in controls but not in patients. Furthermore, in the presence of similar fatigue state over time, controls showed a significant fatigue-related reduction in motor evoked potential (a putative marker of central fatigue) whereas this effect was not seen in patients. in MS patients the pathogenesis of fatigue seems not driven by the mechanisms directly related to corticospinal function (that characterize fatigue in controls) but seems probably due to other "central abnormalities" upstream to primary motor cortex.
多发性硬化症(MS)是一种中枢神经系统的自身免疫性疾病,其中中枢神经系统的炎症、脱髓鞘和轴突损伤同时存在。疲劳是MS中最致残的症状之一,而关于其涉及的神经生理机制知之甚少。为了更深入了解MS中疲劳的机制,我们研究了一组17名MS患者和一组16名年龄匹配的健康对照。从两组中获取基线疲劳严重程度量表和疲劳评分,以检查疲劳水平,并与疲劳诱导的神经生理变化进行统计相关性分析。为了诱导疲劳,我们使用了握力任务。在疲劳任务期间,我们评估疲劳状态(使用测力计),任务结束后,我们评估伯格自觉用力程度量表。在任务前后,使用经颅磁刺激和外周电刺激来评估皮质脊髓束和外周系统功能。患者的临床显著疲劳和中枢运动传导时间比对照组更大,而患者的运动皮层兴奋性降低,最大握力减小。有趣的是,疲劳状态与对照组的自觉疲劳呈正相关,但在患者中并非如此。此外,随着时间的推移,在存在相似疲劳状态的情况下,对照组的运动诱发电位(一种中枢疲劳的假定标志物)出现了与疲劳相关的显著降低,而在患者中未观察到这种效应。在MS患者中,疲劳的发病机制似乎不是由与皮质脊髓功能直接相关的机制驱动的(这是对照组疲劳的特征),而是可能由于初级运动皮层上游的其他“中枢异常”。