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特发性全身性癫痫伴光敏性患者的视觉习惯化受损

Impaired Visual Habituation in Idiopathic Generalized Epilepsy with Photosensitivity Patients.

作者信息

Algin Demet İlhan, Erdinç Oğuz Osman

机构信息

Department of Neurology, Eskişehir Osmangazi University Faculty of Medicine, Eskişehir, Turkey.

出版信息

Noro Psikiyatr Ars. 2018 Apr 20;57(2):108-112. doi: 10.29399/npa.23047. eCollection 2020 Jun.

DOI:10.29399/npa.23047
PMID:32550775
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7285635/
Abstract

INTRODUCTION

In this study, our goal was to analyze further the cortical excitability levels in idiopathic generalized epilepsy (IGE) patients with and without photosensitivity.

METHODS

Forty-two patients (16 men and 26 women; mean age 30±8 years; range: 18-43 years) with IGE and thirty healthy age-matched control subjects (15 men and 15 women; mean age 35±3 years; range: 20-45 years) were enrolled for the investigation. We investigated the following two groups: 18 subjects with IGE with photosensitivity (IGE+PS), and 24 patients with IGE without photosensitivity (IGE-PS). Pattern reversal and potential inter-peak amplitudes, N75-P100 and P100-N145, as well as the corresponding latencies (N75, P100, and N145) for one hundred responses were measured 6 times. A linear regression slope was used for N75-P100 and P100-N145.

RESULTS

Statistical analysis showed difference between groups where the IGE+PS had reduced N75-P100 compared to IGE-PS and controls. In IGE+PS group, the amplitude of N75-P100 was drastically reduced receiving antiepileptic therapy compared to those not receiving any anti-epileptic treatment (p=0.035).

CONCLUSION

These results show that the IGE+PS group has a different photoparoxysmal response phenotype driven by an unknown and distinct molecular mechanism. Pre-activation cortical excitability may be increased in IGE+PS patients compared to the IGE-PS or in healthy group. PR-VEP habituation may project the pathophysiological mechanisms underlying photosensitivity and it may be potential biomarker in patients with IGE+PS.

摘要

引言

在本研究中,我们的目标是进一步分析有和没有光敏性的特发性全身性癫痫(IGE)患者的皮质兴奋性水平。

方法

招募了42例IGE患者(16名男性和26名女性;平均年龄30±8岁;范围:18 - 43岁)和30名年龄匹配的健康对照者(15名男性和15名女性;平均年龄35±3岁;范围:20 - 45岁)进行调查。我们研究了以下两组:18例有光敏性的IGE患者(IGE + PS)和24例无光敏性的IGE患者(IGE - PS)。对100次反应测量了模式反转和峰间电位振幅,即N75 - P100和P100 - N145,以及相应的潜伏期(N75、P100和N145),共测量6次。对N75 - P100和P100 - N145使用线性回归斜率。

结果

统计分析显示各群组之间存在差异,与IGE - PS组和对照组相比,IGE + PS组的N75 - P100降低。在IGE + PS组中,与未接受任何抗癫痫治疗的患者相比,接受抗癫痫治疗的患者N75 - P100的振幅显著降低(p = 0.035)。

结论

这些结果表明,IGE + PS组具有由未知且独特的分子机制驱动的不同光阵发性反应表型。与IGE - PS组或健康组相比,IGE + PS患者的预激活皮质兴奋性可能增加。模式反转视觉诱发电位习惯化可能反映了光敏性的病理生理机制,并且可能是IGE + PS患者的潜在生物标志物。

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