Neurophysiology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133, Milan, Italy.
Epilepsy Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133, Milan, Italy.
Neurol Sci. 2022 Sep;43(9):5553-5562. doi: 10.1007/s10072-022-06236-z. Epub 2022 Jun 27.
To investigate the relationship between N20-P25 peak-to-peak amplitude (N20p-P25p) of somatosensory evoked potentials (SEPs) and the occurrence of abnormalities of the peripheral and/or central sensory pathways and of myoclonus/epilepsy, in 308 patients with increased SEPs amplitude from upper limb stimulation.
We compared cortical response (N20p-P25p) in different groups of patients identified by demographic, clinical, and neurophysiological factors and performed a cluster analysis for classifying the natural occurrence of subgroups of patients.
No significant differences of N20p-P25p were found among different age-dependent groups, and in patients with or without PNS/CNS abnormalities of sensory pathways, while myoclonic/epileptic patients showed higher N20p-P25p than other groups. Cluster analysis identified four clusters of patients including myoclonus/epilepsy, central sensory abnormalities, peripheral sensory abnormalities, and absence of myoclonus and sensory abnormalities.
Increased N20p-P25p prompts different possible pathophysiological substrates: larger N20p-P25p in patients with cortical myoclonus and/or epilepsy is likely sustained by strong cortical hyperexcitability, while milder increase of N20p-P25p could be underpinned by plastic cortical changes following abnormalities of sensory pathways, or degenerative process involving the cortex. SEPs increased in amplitude cannot be considered an exclusive hallmark of myoclonus/epilepsy. Indeed, in several neurological disorders, it may represent a sign of adaptive, plastic, and/or degenerative cortical changes.
研究体感诱发电位(SEP)N20-P25 峰间幅度(N20p-P25p)与周围和/或中枢感觉通路异常及肌阵挛/癫痫发生的关系,纳入 308 例上肢刺激 SEP 幅度增加的患者。
我们比较了不同患者组的皮质反应(N20p-P25p),这些患者是通过人口统计学、临床和神经生理学因素确定的,并进行聚类分析以对患者的自然发生亚组进行分类。
在不同年龄组之间、在有或无周围和/或中枢感觉通路异常的患者之间,N20p-P25p 无显著差异,而肌阵挛/癫痫患者的 N20p-P25p 高于其他组。聚类分析确定了四个患者组,包括肌阵挛/癫痫、中枢感觉异常、周围感觉异常和无肌阵挛和感觉异常。
N20p-P25p 的增加提示不同的可能病理生理基础:皮质肌阵挛和/或癫痫患者的较大 N20p-P25p 可能由皮质过度兴奋维持,而 N20p-P25p 的轻度增加可能由感觉通路异常或涉及皮质的退行性过程后的皮质可塑性变化支撑。幅度增加的 SEP 不能被认为是肌阵挛/癫痫的唯一特征。事实上,在几种神经疾病中,它可能代表皮质适应性、可塑性和/或退行性变化的迹象。