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Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.

机译:癫痫,海马硬化和热性惊厥通过sCN1a周围的常见遗传变异相关联。

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摘要

Epilepsy comprises several syndromes, amongst the most common being mesial temporal lobe epilepsy with hippocampal sclerosis. Seizures in mesial temporal lobe epilepsy with hippocampal sclerosis are typically drug-resistant, and mesial temporal lobe epilepsy with hippocampal sclerosis is frequently associated with important co-morbidities, mandating the search for better understanding and treatment. The cause of mesial temporal lobe epilepsy with hippocampal sclerosis is unknown, but there is an association with childhood febrile seizures. Several rarer epilepsies featuring febrile seizures are caused by mutations in SCN1A, which encodes a brain-expressed sodium channel subunit targeted by many anti-epileptic drugs. We undertook a genome-wide association study in 1018 people with mesial temporal lobe epilepsy with hippocampal sclerosis and 7552 control subjects, with validation in an independent sample set comprising 959 people with mesial temporal lobe epilepsy with hippocampal sclerosis and 3591 control subjects. To dissect out variants related to a history of febrile seizures, we tested cases with mesial temporal lobe epilepsy with hippocampal sclerosis with (overall n = 757) and without (overall n = 803) a history of febrile seizures. Meta-analysis revealed a genome-wide significant association for mesial temporal lobe epilepsy with hippocampal sclerosis with febrile seizures at the sodium channel gene cluster on chromosome 2q24.3 [rs7587026, within an intron of the SCN1A gene, P = 3.36 × 10(-9), odds ratio (A) = 1.42, 95% confidence interval: 1.26-1.59]. In a cohort of 172 individuals with febrile seizures, who did not develop epilepsy during prospective follow-up to age 13 years, and 6456 controls, no association was found for rs7587026 and febrile seizures. These findings suggest SCN1A involvement in a common epilepsy syndrome, give new direction to biological understanding of mesial temporal lobe epilepsy with hippocampal sclerosis with febrile seizures, and open avenues for investigation of prognostic factors and possible prevention of epilepsy in some children with febrile seizures.
机译:癫痫病包括几种综合征,其中最常见的是伴有海马硬化的中颞叶癫痫。伴有海马硬化的中颞叶癫痫发作通常是耐药的,伴有海马硬化的中颞叶癫痫通常与重要的合并症相关,这迫使人们寻求更好的理解和治疗方法。尚不清楚海马硬化性中颞叶癫痫的病因,但与儿童高热惊厥有关。 SCN1A中的突变引起几种以发热性癫痫为特征的罕见癫痫,该突变编码许多抗癫痫药靶向的脑表达的钠通道亚基。我们在1018例海马硬化的颞中叶癫痫患者和7552例对照受试者中进行了全基因组关联研究,并在一个独立样本集中进行了验证,该样本集包括959例海马硬化的中颞叶癫痫患者和3591例对照受试者。为了剖析与高热惊厥史相关的变体,我们测试了伴有颞叶癫痫伴海马硬化的病例(总n = 757),无(总n = 803)高热惊厥史。荟萃分析显示,全基因组范围内的颞叶癫痫和海马硬化与高热惊厥在2q24.3染色体上的钠通道基因簇上相关[rs7587026,在SCN1A基因的内含子内,P = 3.36×10(- 9),优势比(A)= 1.42,95%置信区间:1.26-1.59]。在172名高热惊厥患者和6456名对照中,这些人在前瞻性随访至13岁期间未发生癫痫,并且未发现rs7587026与高热惊厥相关。这些发现表明SCN1A参与了常见的癫痫综合征,为了解中颞叶癫痫伴海马硬化并伴有高热惊厥的生物学理解提供了新的方向,并为研究预后因素和可能预防某些高热惊厥儿童癫痫开辟了道路。

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