376 Pathophysiology of voluntary motor commands in patients with multiple sclerosis identified using reverse engineering of motor unit population discharge.

IF 2.1 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Journal of Clinical and Translational Science Pub Date : 2024-04-03 DOI:10.1017/cts.2024.331
Laura McPherson, Tanner Reece, Skyler Simon, Keith Lohse, Francesco Negro, Catherine Lang, Robert Naismith, Anne Cross
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Abstract

OBJECTIVES/GOALS: Our objective is to characterize excitatory, inhibitory, and neuromodulatory components of the voluntary motor command at the level of the spinal motoneuron in people with multiple sclerosis (MS). This information will provide insight into neural mechanisms of motor dysfunction and their heterogeneity among patients with MS. METHODS/STUDY POPULATION: Due to advances in high-density surface EMG (HDsEMG) decomposition and the recent development of a paradigm for reverse engineering of motor unit population discharge, we can feasibly estimate aspects of excitatory, inhibitory, and neuromodulatory components of the voluntary motor command in humans on a person-specific basis. We tested 11 ambulatory patients with MS and mild-moderate disability. We recorded HDsEMG from tibialis anterior (TA) and soleus (SOL) during isometric plantarflexion and dorsiflexion, performed as slow triangle contractions. EMG was decomposed into motor unit spike trains using blind source separation. We calculated a number of motor unit variables, most notably delta-F, which estimates motoneuron excitability and the balance of neuromodulatory and inhibitory inputs. RESULTS/ANTICIPATED RESULTS: There were consistent differences in MS patients vs. controls. For TA, values were decreased for delta-F (3.9 vs. 5.9 pps), initial firing rate acceleration (5.8 vs. 7.1 pps), firing rate range (9.3 vs. 11.9 pps), and max firing rate (12.3 vs. 15.0 pps). SOL had more modest decreases in delta-F (3.0 vs. 3.8 pps) and firing rate range (4.8 vs. 5.6 pps). Self-sustained firing was longer for MS patients. Within a patient, abnormalities in motor unit variables were not consistent across muscles and legs. Interestingly, there were several abnormalities in the patients with a normal clinical motor exam, indicating that perhaps our measures are sensitive to subclinical changes in processing of voluntary motor commands. DISCUSSION/SIGNIFICANCE: Excitatory, inhibitory, and neuromodulatory components of the voluntary motor command must be appropriately balanced for skilled motor output. This study is the first to characterize how they are disrupted in MS, providing foundational information to inform the development of mechanistically-based rehabilitation interventions.

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376 利用运动单元群放电逆向工程,确定多发性硬化症患者自主运动指令的病理生理学。
目的/目标:我们的目标是描述多发性硬化症(MS)患者脊髓运动神经元水平的自主运动指令的兴奋、抑制和神经调节成分。这些信息将有助于深入了解运动功能障碍的神经机制及其在多发性硬化症患者中的异质性。方法/研究人群:由于高密度表面肌电图(HDsEMG)分解技术的进步以及最近运动单元群放电逆向工程范例的开发,我们可以根据特定人群的情况估算人体自主运动指令的兴奋、抑制和神经调节成分。我们对 11 名患有多发性硬化症和轻度-中度残疾的卧床患者进行了测试。我们记录了胫骨前肌(TA)和比目鱼肌(SOL)在等长跖屈和背屈过程中的 HDsEMG。利用盲源分离将 EMG 分解为运动单元尖峰序列。我们计算了一些运动单元变量,其中最主要的是 delta-F,它可以估计运动神经元的兴奋性以及神经调节和抑制输入的平衡。结果/预期结果:多发性硬化症患者与对照组存在一致的差异。对于 TA,delta-F 值(3.9 对 5.9 pps)、初始点燃率加速度(5.8 对 7.1 pps)、点燃率范围(9.3 对 11.9 pps)和最大点燃率(12.3 对 15.0 pps)均有所下降。SOL 的 delta-F 值(3.0 对 3.8 pps)和发射率范围(4.8 对 5.6 pps)下降幅度较小。多发性硬化症患者的自我持续发射时间更长。在同一患者体内,不同肌肉和腿部的运动单元变量异常并不一致。有趣的是,临床运动检查正常的患者也出现了一些异常,这表明我们的测量方法可能对自主运动指令处理过程中的亚临床变化很敏感。讨论/意义:自主运动指令的兴奋、抑制和神经调节成分必须达到适当的平衡,才能实现熟练的运动输出。本研究首次描述了这些成分在多发性硬化症中是如何被破坏的,为开发基于机理的康复干预措施提供了基础信息。
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来源期刊
Journal of Clinical and Translational Science
Journal of Clinical and Translational Science MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
2.80
自引率
26.90%
发文量
437
审稿时长
18 weeks
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