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脱髓鞘性和轴索性多发性神经病中的磁诱发运动电位:一项比较研究。

Magnetically evoked motor potentials in demyelinating and axonal polyneuropathy: a comparative study.

作者信息

Takada H, Ravnborg M

机构信息

The Department of Clinical Neurophysiology, Rigshospitalet, National University Hospital, Copenhagen, Denmark.

出版信息

Eur J Neurol. 2000 Jan;7(1):63-9. doi: 10.1046/j.1468-1331.2000.00001.x.

Abstract

We investigated the value of magnetically evoked motor potentials (MEPs) for the differentiation of demyelinating and axonal polyneuropathies. The study population comprised 107 patients, with polyneuropathy verified by electromyography (EMG) and nerve conduction study (NCS), who had also been examined by means of MEP. MEPs were evoked by magnetic stimulation of the cortex and the spinal roots and were recorded from three upper limb muscles and two lower limb muscles bilaterally. From the EMG/NCS results 53 patients were characterized as having primary demyelination (demyelinating patients) and 54 as having axonal involvement (axonal patients). Demyelinating patients were classified as acute (acute inflammatory demyelinating polyradiculoneuropathy: AIDP) or chronic (chronic inflammatory demyelinating polyradiculoneuropathy: CIDP) according to the duration of illness. A series of indices were calculated from MEP results. One demyelinating patient and two axonal patients had normal MEPs. The MEPs of the demyelinating patients showed significantly longer peripheral conduction times, larger interside differences and lower amplitudes than the axonal patients. The central conduction index and the amplitudes upon cortical stimulation were significantly higher in patients with CIDP than in those with AIDP. Peripheral conduction time prolonged by more than 85% in at least one of the 10 muscles studied or a peripheral conduction index of above 9.4 were pathognomonic for demyelination. By combining all criteria 75% of the patients could be categorized as CIDP vs. AIDP in accordance with the EMG/NCS diagnosis. Likewise, 83% were categorized correctly as demyelinating versus axonal according to the EMG/NCS data.

摘要

我们研究了磁诱发运动电位(MEP)在区分脱髓鞘性和轴索性多发性神经病中的价值。研究人群包括107例经肌电图(EMG)和神经传导研究(NCS)证实患有多发性神经病且也接受了MEP检查的患者。通过对皮质和脊髓神经根进行磁刺激诱发MEP,并从双侧的三块上肢肌肉和两块下肢肌肉记录MEP。根据EMG/NCS结果,53例患者被判定为原发性脱髓鞘(脱髓鞘患者),54例为轴索受累(轴索性患者)。根据病程,脱髓鞘患者被分为急性(急性炎症性脱髓鞘性多发性神经根神经病:AIDP)或慢性(慢性炎症性脱髓鞘性多发性神经根神经病:CIDP)。从MEP结果计算出一系列指标。1例脱髓鞘患者和2例轴索性患者的MEP正常。脱髓鞘患者的MEP显示出比轴索性患者明显更长的周围传导时间、更大的双侧差异和更低的波幅。CIDP患者的中枢传导指数和皮质刺激时的波幅显著高于AIDP患者。在所研究的10块肌肉中至少有一块肌肉的周围传导时间延长超过85%或周围传导指数高于9.4是脱髓鞘的特征性表现。综合所有标准,75%的患者可根据EMG/NCS诊断归类为CIDP与AIDP。同样,根据EMG/NCS数据,83%的患者被正确归类为脱髓鞘性与轴索性。

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