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Research Priorities in Limb and Task-Specific Dystonias

机译:四肢和特定于肌张力障碍的研究重点

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摘要

Dystonia, which causes intermittent or sustained abnormal postures and movements, can present in a focal or a generalized manner. In the limbs, focal dystonia can occur in either the upper or lower limbs and may be task-specific causing abnormal motor performance for only a specific task, such as in writer’s cramp, runner’s dystonia, or musician’s dystonia. Focal limb dystonia can be non-task-specific and may, in some circumstances, be associated with parkinsonian disorders. The true prevalence of focal limb dystonia is not known and is likely currently underestimated, leaving a knowledge gap and an opportunity for future research. The pathophysiology of focal limb dystonia shares some commonalities with other dystonias with a loss of inhibition in the central nervous system and a loss of the normal regulation of plasticity, called homeostatic plasticity. Functional imaging studies revealed abnormalities in several anatomical networks that involve the cortex, basal ganglia, and cerebellum. Further studies should focus on distinguishing cause from effect in both physiology and imaging studies to permit focus on most relevant biological correlates of dystonia. There is no specific therapy for the treatment of limb dystonia given the variability in presentation, but off-label botulinum toxin therapy is often applied to focal limb and task-specific dystonia. Various rehabilitation techniques have been applied and rehabilitation interventions may improve outcomes, but small sample size and lack of direct comparisons between methods to evaluate comparative efficacy limit conclusions. Finally, non-invasive and invasive therapeutic modalities have been explored in small studies with design limitations that do not yet clearly provide direction for larger clinical trials that could support new clinical therapies. Given these gaps in our clinical, pathophysiologic, and therapeutic knowledge, we have identified priorities for future research including: the development of diagnostic criteria for limb dystonia, more precise phenotypic characterization and innovative clinical trial design that considers clinical heterogeneity, and limited available number of participants.
机译:导致间歇性或持续性异常姿势和运动的肌张力障碍可以以局灶性或全身性方式出现。在肢体中,局灶性肌张力障碍可以在上肢或下肢中发生,并且可能是特定于任务的,导致仅针对特定任务(如作家的抽筋,跑步者的肌张力障碍或音乐家的肌张力障碍)出现异常的运动表现。局灶性肢体肌张力障碍可以是非任务特异性的,在某些情况下可能与帕金森氏病有关。真正的局灶性肢体肌张力障碍患病率尚不清楚,目前可能被低估了,这为知识鸿沟和未来研究提供了机会。局灶性肢体肌张力障碍的病理生理学与其他肌张力障碍有一些共同点,即丧失了对中枢神经系统的抑制作用,并失去了可塑性(称为稳态可塑性)的正常调节。功能成像研究揭示了涉及皮层,基底神经节和小脑的几个解剖网络异常。进一步的研究应集中在生理学和影像学研究中区分因果关系,以使注意力集中在肌张力障碍的大多数相关生物学相关因素上。鉴于表现形式的差异,目前尚无用于治疗肢体肌张力障碍的特异性疗法,但标签外肉毒杆菌毒素疗法通常用于局灶性肢体和特定任务的肌张力障碍。已经应用了各种康复技术,康复干预措施可能会改善治疗效果,但是样本量小,并且缺乏直接比较方法来评估比较疗效的结论。最后,在小型研究中探索了非侵入性和侵入性治疗方式,其设计局限性尚未明确为可支持新临床疗法的大型临床试验提供指导。鉴于我们在临床,病理生理学和治疗学知识上的这些差距,我们确定了未来研究的重点,包括:肢体肌张力障碍的诊断标准的开发,更精确的表型表征和考虑到临床异质性的创新性临床试验设计,以及可用的有限数量参与者。

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