Wissel Jörg, Hernandez Franco Jorge
Neurology and Psychosomatic at Wittenbergplatz, Berlin, University of Potsdam, Potsdam, Germany.
Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suárez, Mexico City, Mexico.
Front Neurol. 2024 Nov 18;15:1463292. doi: 10.3389/fneur.2024.1463292. eCollection 2024.
It is common in clinical practice to evaluate active movement in spastic movement disorders (SMDs) associated with the upper motor neuron syndrome in terms of resistance to passive movement in the rest position, with the assumption that this may reflect motor control when the patient is in active motion. In addition, the definition of spasticity as a velocity-dependent resistance to passive movement does not account for the impact of abnormal muscle synergies (synkinesia), on active motion of upper and lower limbs in SMDs. In this article, we put forward our theory that synkinetic movement patterns are controlled by activation from spinal afferents and inhibition from the cortex, and become disturbed following a loss of inhibition and change to spinal afferents following damage to the corticospinal tract. In this regard, we propose a change in the focus from passive to active function at the evaluation stage of the SMD management plan, and a new treatment approach to modulate muscle synergies with botulinum neurotoxin type A therapy.
在临床实践中,通常根据静息位被动运动的阻力来评估与上运动神经元综合征相关的痉挛性运动障碍(SMD)中的主动运动,假定这可能反映患者主动运动时的运动控制。此外,将痉挛定义为对被动运动的速度依赖性阻力,并未考虑异常肌肉协同作用(联带运动)对SMD中上肢和下肢主动运动的影响。在本文中,我们提出我们的理论,即联带运动模式由脊髓传入神经的激活和皮质的抑制所控制,并且在抑制丧失以及皮质脊髓束受损后脊髓传入神经发生变化后会受到干扰。在这方面,我们建议在SMD管理计划的评估阶段将重点从被动功能转变为主动功能,并提出一种用A型肉毒杆菌毒素疗法调节肌肉协同作用的新治疗方法。