de Mari M, Margari L, Lamberti P, Iliceto G, Ferrari E
Institute of Neurology, University of Bari, Italy.
J Neural Transm Suppl. 1995;45:171-6.
Somatosensory evoked potentials (SEPs) to median nerve stimulation have been performed before and after apomorphine-test in 10 parkinsonian patients. Latency and amplitude of the P14-N20 parietal complex and of the P20-N30 frontal complex were evaluated. The N30 amplitude was significantly reduced before apomorphine administration (p < 0.001) with a consequent increase of the N20/N30 amplitude ratio (p < 0.001). Eight patients clinically improved after Apomorphine. Following Apomorphine there was no change in the amplitude of the parietal complex P14-N20. On the other hand the frontal complex P20-N30 showed a significant amplitude potentiation (p < 0.005), with a reduction of the N20/ N30 amplitude ratio (ns). This finding was almost constant among the 8 responder patients. These results suggest the utility of combining clinical and neurophysiological data to assess the responsiveness to dopaminergic treatment.
对10例帕金森病患者在阿扑吗啡试验前后进行了正中神经刺激体感诱发电位(SEP)检查。评估了P14-N20顶叶复合体和P20-N30额叶复合体的潜伏期和波幅。阿扑吗啡给药前N30波幅显著降低(p<0.001),N20/N30波幅比值随之增加(p<0.001)。8例患者经阿扑吗啡治疗后临床症状改善。阿扑吗啡治疗后,顶叶复合体P14-N20的波幅无变化。另一方面,额叶复合体P20-N30显示出显著的波幅增强(p<0.005),N20/N30波幅比值降低(无统计学意义)。这一发现在8例有反应的患者中几乎是一致的。这些结果表明,结合临床和神经生理学数据来评估对多巴胺能治疗的反应性是有用的。