Berardelli A, Noth J, Thompson P D, Bollen E L, Currà A, Deuschl G, van Dijk J G, Töpper R, Schwarz M, Roos R A
Dipartimento di Scienze Neurologiche Università di Roma La Sapienza, Rome, Italy.
Mov Disord. 1999 May;14(3):398-403. doi: 10.1002/1531-8257(199905)14:3<398::aid-mds1003>3.0.co;2-f.
This article reviews the neurophysiological abnormalities described in Huntington's disease. Among the typical features of choreic movements are variable and random patterns of electromyographic (EMG) activity, including cocontraction of agonist and antagonist muscles. Studies of premotor potentials show that choreic movements are not preceded by a Bereitschaftspotential, therefore demonstrating that choreic movement is involuntary. Early cortical median-nerve somatosensory-evoked potentials have reduced amplitudes and the reduction correlates with reduced glucose consumption in the caudate nucleus. Long-latency stretch reflexes evoked in the small hand muscles are depressed. These findings may reflect failed thalamocortical relay of sensory information. In Huntington's disease, the R2 response of the blink reflex has prolonged latencies, diminished amplitudes, and greater habituation than normal. These abnormalities correlate with the severity of chorea in the face. Patients with Huntington's disease perform simple voluntary movements more slowly than normal subjects and with an abnormal triphasic EMG pattern. Bradykinesia is also present during their performance of simultaneous and sequential movements. Eye movements show abnormalities similar to those seen in arm movements. In Huntington's disease, arm movement execution is associated with reduced PET activation of cortical frontal areas. Studies using transcranial magnetic stimulation show that patients with Huntington's disease have normal corticospinal conduction but some patients have a prolonged cortical silent period. Bradykinesia results from degeneration of the basal ganglia output to the supplementary motor areas concerned with the initiation and maintenance of sequential movements. The coexisting hyperkinetic and hypokinetic movement disorders in patients with Huntington's disease probably reflect the involvement of direct and indirect pathways in the basal ganglia-thalamus-cortical motor circuit.
本文综述了亨廷顿舞蹈病中所描述的神经生理异常情况。舞蹈样动作的典型特征包括肌电图(EMG)活动模式多变且随机,其中包括主动肌和拮抗肌的共同收缩。运动前电位研究表明,舞蹈样动作之前并无运动准备电位,因此证明舞蹈样动作是不自主的。早期皮质正中神经体感诱发电位的波幅降低,且这种降低与尾状核葡萄糖消耗减少相关。在手的小肌肉中诱发的长潜伏期牵张反射减弱。这些发现可能反映了感觉信息丘脑皮质中继功能的缺失。在亨廷顿舞蹈病中,瞬目反射的R2反应潜伏期延长、波幅减小,且比正常情况更易产生习惯化。这些异常与面部舞蹈症的严重程度相关。与正常受试者相比,亨廷顿舞蹈病患者执行简单自主运动的速度更慢,且肌电图呈异常的三相模式。在执行同时性和连续性动作时也存在运动迟缓。眼球运动显示出与手臂运动类似的异常。在亨廷顿舞蹈病中,手臂运动的执行与额叶皮质PET激活减少有关。经颅磁刺激研究表明,亨廷顿舞蹈病患者的皮质脊髓传导正常,但部分患者的皮质静息期延长。运动迟缓是由于基底神经节向与连续性动作的发起和维持有关的辅助运动区输出退化所致。亨廷顿舞蹈病患者同时存在的运动亢进和运动减退性运动障碍可能反映了基底神经节 - 丘脑 - 皮质运动回路中直接和间接通路均受累。