神经性戈谢病患者的脑电图和表型模式-在单一中心的十年经验。

IF 1.2 Q4 CLINICAL NEUROLOGY
Xiying Yang, Yan Meng, Jian Chen, Qian Lu, Linyan Hu, Xiuyu Shi, Jing Wang, Guang Yang, Liping Zou
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引用次数: 0

摘要

背景:本研究旨在研究神经性戈谢病(GD)患者独特的脑电图(EEG)模式,探讨脑电图表现与神经表型的相关性,以优化临床预后。方法:回顾性分析2012年1月至2022年7月间50例GD患者74次脑电图记录。结果:23例患者出现异常脑电图记录,其中GD1型(过渡型)11例,神经性GD 12例。对12例神经性GD患者中9例癫痫患者进行临床病程分析。在神经病变脑电图记录中观察到的主要波形是在清醒和睡眠状态下的峰波复合体(SWC)。这与过渡型患者仅在睡眠时观察到的尖波有显著差异(P = 0.0230)。神经病变患者的异常放电多位于双侧罗兰区,过渡性放电多累及双侧额叶区。三名具有癫痫脑电图模式的患者在数年后报告了他们的首次癫痫发作。尽管持续存在异常脑电图模式,但神经病变患者的癫痫发作可通过抗癫痫药物(asm)有效控制。眼部症状时的脑电图特征为睡眠时散发或持续的单侧SWC。结论:神经性GD患者表现出不同的脑电图模式,有助于与GD1患者区分。早期治疗可有效控制癫痫发作。脑电图在监测癫痫发作中起着至关重要的作用,可以促进对GD患者的及时干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Electroencephalogram and phenotype patterns in neuronopathic Gaucher disease patients - ten years of experience in a single center.

Electroencephalogram and phenotype patterns in neuronopathic Gaucher disease patients - ten years of experience in a single center.

Electroencephalogram and phenotype patterns in neuronopathic Gaucher disease patients - ten years of experience in a single center.

Electroencephalogram and phenotype patterns in neuronopathic Gaucher disease patients - ten years of experience in a single center.

Background: This study aimed to investigate the unique electroencephalography (EEG) patterns in neuronopathic Gaucher disease (GD) patients and explore the correlations between EEG findings and neurological phenotypes so as to optimize clinical outcomes.

Methods: A retrospective analysis was conducted on 74 EEG recordings from 50 GD patients between January 2012 and July 2022.

Results: Twenty-three patients exhibited abnormal EEG recordings, including 11 of the GD1 type (the transitional type) and 12 with neuronopathic GD. Of the 12 neuronopathic GD patients, 9 patients with epilepsy were analysed specifically in terms of the clinical course. The primary waveform observed in the neuronopathic EEG recordings was the spike-and-wave complex (SWC) during both awake and sleep states. This was significantly different from sharp waves observed only during sleep in the patients of the transitional type (P = 0.0230). The abnormal discharges in the neuronopathic patients were most commonly located in the bilateral Rolandic areas, while the transitional type commonly involved the bilateral frontal regions. Three patients with an epileptic EEG pattern reported their initial seizures years later. Seizures in the neuronopathic patients were effectively controlled with anti-seizure medications (ASMs), despite the ongoing presence of abnormal EEG patterns. The EEG patterns during ocular symptoms were characterized by sporadic or continuous unilateral SWC during sleep.

Conclusions: Patients with neuronopathic GD exhibit distinct EEG patterns that can help differentiate them from GD1 patients. Early treatment with ASMs can effectively control seizures. EEG plays a crucial role in monitoring seizures and can facilitate prompt intervention for GD patients.

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来源期刊
Acta Epileptologica
Acta Epileptologica Medicine-Neurology (clinical)
CiteScore
2.00
自引率
0.00%
发文量
38
审稿时长
20 weeks
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