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肌张力障碍儿童的肌肉协同作用呈现出“健康”模式,尽管其运动表现有所改变。

Muscle synergies in children with dystonia capture "healthy" patterns regardless the altered motor performance.

作者信息

Lunardini Francesca, Casellato Claudia, Bertucco Matteo, Sanger Terence D, Pedrocchi Alessandra

出版信息

Annu Int Conf IEEE Eng Med Biol Soc. 2015;2015:2099-102. doi: 10.1109/EMBC.2015.7318802.

Abstract

Muscle synergies are hypothesized to represent motor modules recruited by the nervous system to flexibly perform subtasks necessary to achieve movement. Muscle synergy analysis may offer a better view of the neural structure underlying motor behaviors and how they change in motor deficits and rehabilitation. The aim of this study is to investigate if muscle synergies are able to encode regularities in the musculoskeletal system organization and dynamic behavior of patients with dystonia, or if they are altered as a consequence of the nervous system dysfunction in dystonia. To do so, we applied muscle synergies analysis to muscle activity recorded during the execution of upper limb writing tasks in 10 children with dystonia and 9 age-matched healthy controls. We show that, although children with dystonia present movement abnormalities compared to control subjects, the muscle synergies extracted from the two groups are very similar, and that the two groups share a significant number of motor modules. Our finding therefore suggests that a regular modular organization of upper limb muscle coordination is preserved for childhood dystonia.

摘要

肌肉协同作用被假定为代表神经系统招募的运动模块,以灵活地执行实现运动所需的子任务。肌肉协同作用分析可能会更好地展现运动行为背后的神经结构,以及它们在运动功能障碍和康复过程中的变化。本研究的目的是调查肌肉协同作用是否能够编码肌张力障碍患者肌肉骨骼系统组织和动态行为的规律,或者它们是否因肌张力障碍中神经系统功能障碍而改变。为此,我们对10名患有肌张力障碍的儿童和9名年龄匹配的健康对照在执行上肢书写任务期间记录的肌肉活动进行了肌肉协同作用分析。我们表明,尽管与对照组相比,患有肌张力障碍的儿童存在运动异常,但从两组中提取的肌肉协同作用非常相似,并且两组共享大量运动模块。因此,我们的发现表明,儿童肌张力障碍患者上肢肌肉协调的规则模块化组织得以保留。

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