《当蓝变灰:音乐家肌张力障碍之谜

D. A. Peterson, E. Altenmüller
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引用次数: 1

摘要

音乐家肌张力障碍(MD)是一种神秘的神经障碍,选择性地干扰音乐表演所需的自主运动控制。在许多情况下,它只在某些作品的某些段落中是明显的。这给评估和治疗带来了挑战。口服药物和注射肉毒杆菌毒素已显示出有限的疗效,但有不良副作用。物理医学和康复策略通常具有较低的不良副作用风险,并显示出疗效的希望,但难以纳入良好对照的研究。MD与其他形式的局灶性肌张力障碍具有相同的病理生理特征,包括中枢神经系统许多层面的抑制、感觉运动整合和可塑性异常。发病机制的理论包括多种病因,如遗传、性别和“使用模式”。正在进行的评估、病理生理学和发病机制的研究应该为管理甚至预防MD提供理论基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
When Blue Turns to Gray: The Enigma of Musician’s Dystonia
Musician’s dystonia (MD) is an enigmatic neurologic disorder that selectively interferes with voluntary motor control required for music performance. In many cases it is evident only in certain passages of certain pieces. This contributes to the challenges of assessment and treatment. Oral medications and botulinum toxin injections have shown some limited efficacy, but with adverse side effects. Physical medicine and rehabilitation strategies generally have a lower risk of adverse side effects and show promise in efficacy but are difficult to incorporate in well-controlled studies. MD shares pathophysiologic features with other forms of focal dystonia, including abnormalities in inhibition, sensorimotor integration, and plasticity at many levels of the central nervous system. Theories for the pathogenesis include multiple etiologic factors, such as genetics, gender, and “use patterns.” Ongoing research on assessment, pathophysiology, and pathogenesis should provide rationale bases for managing and even preventing MD.
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