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多发性硬化症患者脊髓运动神经元水平的自主运动指令的病理生理学

Pathophysiology of voluntary motor commands at the level of the spinal motoneuron in patients with multiple sclerosis.

作者信息

McPherson Laura M, Lohse Keith R, Simon Skyler M, Beauchamp James A, Negro Francesco, Naismith Robert T, Cross Anne H

机构信息

Program in Physical Therapy, Washington University School of Medicine, St. Louis, MO.

Department of Neurology, Washington University School of Medicine, St. Louis, MO.

出版信息

medRxiv. 2025 Aug 13:2025.08.12.25333527. doi: 10.1101/2025.08.12.25333527.

Abstract

Multiple sclerosis (MS) is a progressive inflammatory neurodegenerative disease that degrades neural transmission between the brain and spinal α-motoneurons. These voluntary motor commands contain excitatory, inhibitory, and neuromodulatory components that must be appropriately balanced for skilled motor control. Unlike other clinical populations, in MS we have no knowledge about how voluntary motor commands are disrupted. MS is a clinically heterogeneous population, with sensorimotor impairments that vary widely and unpredictably across patients. Our overall scientific hypothesis is that the voluntary motor command in the MS population varies accordingly, with multiple "phenotypes" evident. Here, we explore this idea by identifying pathological aspects of the voluntary motor command in 59 participants with MS with a range of sensorimotor symptoms and disability, compared with 38 age-/sex-matched controls. We recorded motor unit discharge from the tibialis anterior and soleus muscles during isometric dorsiflexion/plantarflexion contractions. We then calculated geometric and temporal features in their firing patterns to characterize their excitatory, inhibitory, and neuromodulatory inputs according to a recently developed "reverse engineering" paradigm. MS values for many of our parameters were highly variable, with some participants with abnormally values and others with abnormally low values. In addition to this variability, MS group means for most parameters reflecting the balance of neuromodulation and inhibition were significantly lower than those of controls. These initial findings support the idea that there may be different phenotypes of voluntary motor command pathology among patients with MS, indicating the potential need to personalize the selection of mechanistically targeted rehabilitation therapies.

摘要

多发性硬化症(MS)是一种进行性炎症性神经退行性疾病,会破坏大脑与脊髓α运动神经元之间的神经传递。这些自主运动指令包含兴奋性、抑制性和神经调节性成分,为实现熟练的运动控制,这些成分必须保持适当平衡。与其他临床群体不同,我们并不清楚MS患者的自主运动指令是如何被破坏的。MS患者在临床上具有异质性,其感觉运动障碍在患者之间差异很大且不可预测。我们的总体科学假设是,MS患者群体中的自主运动指令也相应不同,存在多种明显的“表型”。在此,我们通过识别59名有一系列感觉运动症状和残疾的MS患者自主运动指令的病理特征来探究这一观点,并与38名年龄和性别匹配的对照组进行比较。我们在等长背屈/跖屈收缩过程中记录了胫前肌和比目鱼肌的运动单位放电情况。然后,我们根据最近开发的“逆向工程”范式,计算其放电模式中的几何和时间特征,以表征其兴奋性、抑制性和神经调节性输入。我们许多参数的MS值高度可变,一些参与者的值异常高,而另一些则异常低。除了这种变异性外,反映神经调节和抑制平衡的大多数参数的MS组均值显著低于对照组。这些初步发现支持了这样一种观点,即MS患者中可能存在不同表型的自主运动指令病理,这表明可能需要针对个体选择有机制针对性的康复治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d245/12363701/6919e97a8119/nihpp-2025.08.12.25333527v1-f0001.jpg

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