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亨廷顿舞蹈症中运动迟缓与舞蹈症的并存及其对基底神经节运动控制理论的影响。

The coexistence of bradykinesia and chorea in Huntington's disease and its implications for theories of basal ganglia control of movement.

作者信息

Thompson P D, Berardelli A, Rothwell J C, Day B L, Dick J P, Benecke R, Marsden C D

机构信息

University Department of Neurology, Institute of Psychiatry, London, UK.

出版信息

Brain. 1988 Apr;111 ( Pt 2):223-44. doi: 10.1093/brain/111.2.223.

Abstract

Investigation of motor function in a group of 17 patients with Huntington's disease reveals that, in addition to the chorea that many patients exhibit, defects in voluntary motor performance also are evident. Fast simple wrist flexion movements to 15 degrees or 60 degrees were slower, and individual movements showed greater variability than seen in normal subjects. This bradykinesia was most pronounced in those patients who were akinetic and rigid, but also was seen in those with chorea alone; bradykinesia was independent of the drug treatment that the patients were receiving (and was therefore not due to drug-induced parkinsonism). The electromyographic activity of the agonist muscles during such simple but slow movement differed from that seen in Parkinson's disease. The performance of complex movements revealed further deficits. Some patients were unable to combine two movements in a simultaneous or sequential movement task of squeezing the hand and flexing the elbow. Those who could perform these complex movements exhibited slowing of the velocity of the movement and prolongation of the interval between movements. These abnormalities were present in patients with chorea who were not taking neuroleptic drugs. It is argued that they represent an abnormality of motor programming of complex movements, over and above the defect in executing simple movements. The long latency stretch reflexes in wrist flexor muscles and flexor pollicis longus were reduced or absent, but this did not correlate with changes in motor performance, or with the reduced size of the early components of cortical sensory evoked potentials. Bradykinesia is thus shown to be an integral component of the motor disorder of Huntington's disease, in addition to the chorea. The coexistence of bradykinesia and chorea in this illness is compatible with current theories of the role of the basal ganglia in the control of movement.

摘要

对一组17名亨廷顿舞蹈症患者的运动功能进行调查后发现,除了许多患者表现出的舞蹈症外,自主运动表现缺陷也很明显。快速简单地将手腕弯曲15度或60度的动作较慢,且单个动作的变异性比正常受试者更大。这种运动迟缓在那些运动不能和强直的患者中最为明显,但在仅患有舞蹈症的患者中也可见;运动迟缓与患者正在接受的药物治疗无关(因此不是药物诱发的帕金森症)。在这种简单但缓慢的运动过程中,主动肌的肌电图活动与帕金森病患者不同。复杂运动的表现揭示了进一步的缺陷。一些患者在同时或顺序进行手部挤压和肘部弯曲的运动任务时,无法将两个动作结合起来。那些能够完成这些复杂运动的患者表现出运动速度减慢以及动作之间的间隔延长。这些异常情况存在于未服用抗精神病药物的舞蹈症患者中。有人认为,它们代表了复杂运动的运动编程异常,这超出了执行简单运动的缺陷。腕屈肌和拇长屈肌的长潜伏期牵张反射减弱或消失,但这与运动表现的变化以及皮层感觉诱发电位早期成分的减小无关。因此,运动迟缓被证明是亨廷顿舞蹈症运动障碍的一个组成部分,除了舞蹈症之外。这种疾病中运动迟缓与舞蹈症的共存与目前关于基底神经节在运动控制中作用的理论相符。

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