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EMG-based Indicators of Muscular Co-Activation during Gait in Children with Duchenne Muscular Dystrophy

机译:基于肌电图的杜兴氏肌营养不良症儿童步态中肌肉共激活的指标

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Muscular weakness is one of the main signs associated with the onset and progression of Duchenne Muscular Dystrophy. During motor functions, this disease also determines deviations in muscular activity, especially in terms of coordination and activation between muscles acting on the same joints. In this study, surface EMG activity of the lower limb muscles of 10 children with Duchenne Muscular Dystrophy at different times from disease onset were recorded along with kinematics during unconstrained gait. Muscular co-activation of muscle pairs was then evaluated by extracting different co-activation indicators, and linking them with kinematic markers of motor function. The combination of disease progression and pharmacological treatment resulted in a significant decrease in terms of co-activation indexes for two pairs of agonist-antagonist muscles, and for one of these two pairs the decrease in co-activation was correlated with a decrease in the motor function of gait.
机译:肌肉无力是与杜兴肌营养不良症的发作和发展有关的主要症状之一。在运动功能期间,这种疾病还决定了肌肉活动的偏差,特别是在作用于同一关节的肌肉之间的协调和激活方面。在这项研究中,记录了10名杜兴氏肌营养不良症患儿在疾病发作不同时间的下肢肌肉表面肌电活动,并记录了步态不受约束的运动学。然后,通过提取不同的共激活指标并将其与运动功能的运动学标记联系起来,评估肌肉对的肌肉共激活。疾病进展和药物治疗的结合导致两对激动剂-拮抗肌的共激活指数显着降低,并且对于这两对中的一对,共激活的降低与运动能力的降低相关步态功能。

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