J Korean Neurol Assoc > Volume 10(1); 1992 > Article
Journal of the Korean Neurological Association 1992;10(1): 59-71.
각종 운동신경계 병변에서 자기자극에 의한 운동유발전위의 변동
김광수, 박영춘
계명대학교 신경과.
Magnetic Motor Evoked Potentials in Motor Pathway Lesions
Kwan-Soo Kim, M.D., Young-Choon Park, M.D.,
Department of Neurology, College of Medicne, Keimyung University
Abstract
This study was undertaken to evaluate the clinical usefulness of magnetic evoked potentials(MEP) in localization of motor pathway lesions and the relation between motor weakness and MEP alterations. The patient group consisted of 50 patients(33 men and 17 women) with vanous diseases involving motor pathway, among which were 21 cerebral infarction, 15 intracerebrai hemorrhage, 3 cervical spondylosis, 3 amyotrophic lateral sclerosis and 8 peripheral polyneuropathy, confirmed by neurological findings, CT or MRI, EMG and nerve conduction velocity. The results were compared with 20 healthy subjects (11 men and 9 women) as a control group. MEP were recorded by using Digitimer magnetic stimulator model Dl90 and Medelec ER 94a/Sensor apparatuses, and MEP were evoked by magnetic stimulations over the vertex, the 7th cervical vertebra and Erb's point, and central motor conduction time (CMCT) was calculated by substracting the onset latency of abductor pollicis brevis muscle responses obtained by stimulation over the C7 vertebra from that obtained by stimulation over the scalp. The mean latencies of MEP after transcranial magnetic stimulations were prolonged in patients with motor pathway lesion, and mean CMCT were prolonged in patients with stroke. Cortical MEP were not elicited in stroke patients with profound motor weakn-ess below motor power 2/5 in arm, Prolongation of mean latency of cortical MEP and mean CMCT were correlated with motor weakness below motor power 4/5. In stroke patients, there were prolongation of mean CMCT and mean latency of cortical MEP evoked by stimulation to the undamaged hemisphere. These results suggest that magnetic MEP test is safe and useful in evaluation of motor pathway lesions.


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