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

IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY Revista de neurologia Pub Date : 2024-10-01 DOI:10.33588/rn.7907.2024107
J C Reséndiz-Aparicio, Y López-Vargas, G Vargas-Ramírez, J Rogel-Cuevas, J I Castro-Macías, G Soca-Chafre, E Castro-Martínez
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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.

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[墨西哥癫痫病的病因:全国多中心登记的结果]。
导言:癫痫影响着数百万人,其地理模式通常与病因有关。我们的目标是描述墨西哥癫痫的主要病因:我们从 2021 年至 2022 年在墨西哥 31 个州的 89 家医院进行的多中心癫痫登记中选取了患者,样本主要为儿童。只有接受过脑电图和神经影像学检查的患者才被纳入其中:我们分析了 6653 名有病因记录的患者。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)。(2.9%(2.5-3.3)、代谢性 1.4%(1.1-1.7)、免疫性 0.9%(0.8-1.3)和未知 40.9%(39.8-42.2)。两个主要的结构性病因是大脑皮层发育畸形和缺氧缺血性脑病。神经囊虫病只占少数,仅为1%。结构性病因和遗传性病因分别与局灶性和全身性癫痫发作有关。已发现的癫痫状态大多伴有运动成分,与免疫和感染病因有关。61.6%的患者有合并症,主要是神经系统发育障碍。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。结论:癫痫的主要病因是结构性病因,遗传性病因的发病率相对低于其他系列,这可能是由于遗传测试的可用性有限。尽管技术在不断进步,但仍有很大一部分癫痫病因不明。
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来源期刊
Revista de neurologia
Revista de neurologia 医学-临床神经学
CiteScore
2.50
自引率
8.30%
发文量
117
审稿时长
3-8 weeks
期刊介绍: Revista de Neurología fomenta y difunde el conocimiento generado en lengua española sobre neurociencia, tanto clínica como experimental.
期刊最新文献
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