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[墨西哥癫痫的病因:国家多中心登记结果]

[Etiology of epilepsy in Mexico: results from the national multi-centre register].

作者信息

Reséndiz-Aparicio J C, López-Vargas Y, Vargas-Ramírez G, Rogel-Cuevas J, Castro-Macías J I, Soca-Chafre G, Castro-Martínez E

机构信息

Hospital Psiquiátrico Infantil Dr. Juan N. Navarro, Ciudad de México, México.

Instituto Nacional de Neurologia y Neurocirugia "Dr. Manuel Velasco Suárez", Ciudad de México, México.

出版信息

Rev Neurol. 2024 Oct 1;79(7):199-206. doi: 10.33588/rn.7907.2024107.

Abstract

INTRODUCTION

Epilepsy affects millions of people and its geographical patterns are usually linked to etiological aspects. Our objective was to describe main etiologies of epilepsy in Mexico.

PATIENTS AND METHODS

We selected patients from the Multicenter Epilepsy Registry carried out from 2021 to 2022 in 89 Mexican hospitals in 31 states, a sample predominantly of pediatric age. Only patients with electroencephalography and neuroimaging studies were included.

RESULTS

We analyzed 6,653 patients with documented etiologies. Etiology frequency with confidence interval (95% CI) was: structural 46.1% (44.9-47.3), genetic 12.9% (12.1-13.7), infectious 2.9%. (2.5-3.3), metabolic 1.4% (1.1-1.7), immune 0.9% (0.8-1.3) and unknown 40.9% (39.8-42.2). The two main structural etiologies were malformations of cortical development and hypoxic-ischemic encephalopathy. Neurocysticercosis represented a minority with only 1%. Structural and genetic etiologies were associated with focal and generalized onset seizures respectively. Status epilepticus was identified, mostly with motor component, associated with immune and infectious etiologies. Comorbidities were found in 61.6%, mainly neurological development disorders. Drug-resistant epilepsy was more common in patients with immune, infectious and structural etiologies.

CONCLUSIONS

The main etiology of epilepsy was structural. The frequency of genetic etiology was relatively lower than in other series, possibly due to the limited availability of genetic tests. Despite technological advances, a large fraction of epilepsies still has unknown origin.

摘要

引言

癫痫影响着数百万人,其地理分布模式通常与病因学方面相关。我们的目的是描述墨西哥癫痫的主要病因。

患者与方法

我们从2021年至2022年在墨西哥31个州的89家医院开展的多中心癫痫登记中选取患者,样本主要为儿童年龄段。仅纳入进行了脑电图和神经影像学检查的患者。

结果

我们分析了6653例有记录病因的患者。病因频率及置信区间(95%CI)为:结构性46.1%(44.9 - 47.3),遗传性12.9%(12.1 - 13.7),感染性2.9%(2.5 - 3.3),代谢性1.4%(1.1 - 1.7),免疫性0.9%(0.8 - 1.3),不明原因40.9%(39.8 - 42.2)。两个主要的结构性病因是皮质发育畸形和缺氧缺血性脑病。神经囊尾蚴病占少数,仅1%。结构性和遗传性病因分别与局灶性和全身性发作性癫痫相关。发现了癫痫持续状态,主要伴有运动成分,与免疫性和感染性病因相关。61.6%的患者存在合并症,主要是神经发育障碍。耐药性癫痫在免疫性、感染性和结构性病因的患者中更为常见。

结论

癫痫的主要病因是结构性的。遗传性病因的频率相对低于其他系列研究,可能是由于基因检测的可及性有限。尽管有技术进步,但很大一部分癫痫的病因仍不明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b5/11605898/768c34ebde91/RN-79-199-g001.jpg

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