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[运动神经元病中的宏肌电图检查]

[Macro electromyography in motor neuron disease].

作者信息

Goh M H, Chiu H C

机构信息

Department of Internal Medicine, Taipei Medical College Hospital.

出版信息

Zhonghua Yi Xue Za Zhi (Taipei). 1991 Oct;48(4):284-90.

PMID:1659924
Abstract

Macroelectromyography (macroEMG) is a technique that provides information about the size of a motor unit which the conventional EMG is not able to. We used macroEMG to study 11 cases of motor neuron disease (MND), presenting with upper extremities symptoms (no lower extremities symptoms). Muscles we selected to study were the biceps brachii and the tibialis anterior. Amplitude, area and fiber density (FD) were analysed. The controlled groups consisted of 11 cases of myasthenia gravis (MG) and 11 normal subjects. Our study demonstrated that in the MND group, amplitude, area and FD of both muscles were significantly increased over those of the normal subjects. We also found that the amplitude and area of biceps brachii in patients who had clinical symptoms less than 2 years, were significantly higher than those over 2 years. However, there were no significant differences between the two groups of the tibialis anterior. This was probably due to the fact that the disease process was not severe enough to cause significant differences. Further follow up studies are necessary to clarify this question. In MG, amplitude, area and FD were not significantly different than those of the normal subjects. Increased amplitude, area and FD in MND provides information regarding the reinnervation process of the disease. As the disease progresses, the above findings may decrease because the motor neurons can no longer support the enlarged motor unit. All of the MND patients in our study, had no symptoms in the lower extremities; however, we found there were significant changes in the macro-EMG findings of the tibialis anterior. This indicates that macro-EMG can detect early electrophysiological changes in the motor unit before clinical symptoms develop.

摘要

宏肌电图(macroEMG)是一种能够提供有关运动单位大小信息的技术,而传统肌电图无法做到这一点。我们使用宏肌电图研究了11例表现为上肢症状(无下肢症状)的运动神经元病(MND)患者。我们选择研究的肌肉是肱二头肌和胫前肌。分析了其波幅、面积和纤维密度(FD)。对照组包括11例重症肌无力(MG)患者和11名正常受试者。我们的研究表明,在MND组中,两块肌肉的波幅、面积和FD均显著高于正常受试者。我们还发现,临床症状少于2年的患者肱二头肌的波幅和面积显著高于病程超过2年的患者。然而,胫前肌两组之间没有显著差异。这可能是因为疾病进程不够严重,不足以导致显著差异。需要进一步的随访研究来阐明这个问题。在MG患者中,波幅、面积和FD与正常受试者相比无显著差异。MND患者波幅、面积和FD的增加提供了有关疾病重新支配过程的信息。随着疾病进展,上述发现可能会降低,因为运动神经元不再能够支持扩大的运动单位。我们研究中的所有MND患者下肢均无症状;然而,我们发现胫前肌的宏肌电图结果有显著变化。这表明宏肌电图可以在临床症状出现之前检测到运动单位早期的电生理变化。

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