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局灶性癫痫和热性惊厥中 CPA6 启动子甲基化增加。

Increased CPA6 promoter methylation in focal epilepsy and in febrile seizures.

机构信息

Laboratory of Genetic, Immunology and Human Pathologies, Department of Biology, Faculty of Sciences, Tunis, Tunisia; Neurological Department, Charles Nicolle Hospital, Tunis, Tunisia.

Department of Psychiatry, University of Geneva, Geneva, Switzerland.

出版信息

Epilepsy Res. 2014 Jan;108(1):144-8. doi: 10.1016/j.eplepsyres.2013.10.007. Epub 2013 Oct 24.

Abstract

Focal epilepsy (FE) is one of the most common forms of adult epilepsy and is usually regarded as a multifactorial disorder. Febrile seizures (FS) often appear during childhood in a subtype of FE patients, i.e. with temporal lobe epilepsy (TLE) and hippocampal sclerosis (HS). FS are the most common human convulsive event associated with fever. Genetic evidences for FS have suggested a complex mode of inheritance. Until now, to investigate genes at the genomic level, linkage analysis of familial forms and association studies have been performed, but nothing conclusive has been clearly related to FE and FS. As complex disorders, environmental factors might play a crucial role through epigenetic modification of key candidate genes such as CPA6, which encodes Carboxypeptidase A6, an extracellular protein. Therefore, we assessed DNA methylation in promoter of CPA6. In 186 FE patients and 92 FS patients compared to 93 healthy controls and 42 treated controls with antiepileptic drugs (AEDs), we found significant higher levels of methylation for epileptic patients. Methylation status were 3.4% (±3.2%) for FE cases and 4.3% (±3.5%) for FS cases, whereas healthy individuals and treated controls with AEDs showed a level of 0.8% (±2.9%) and 1.5% (±3.9%), respectively (p≤0.001 for all comparisons). These results let growing evidence for DNA methylation involvment in FE and FS.

摘要

局灶性癫痫(FE)是成人癫痫中最常见的形式之一,通常被认为是一种多因素疾病。热性惊厥(FS)通常在儿童期出现在 FE 患者的一个亚型中,即伴有颞叶癫痫(TLE)和海马硬化(HS)的患者。FS 是最常见的与发热相关的人类惊厥事件。FS 的遗传证据表明其遗传方式复杂。到目前为止,为了在基因组水平上研究基因,已经对家族形式进行了连锁分析和关联研究,但没有明确的结论与 FE 和 FS 相关。作为复杂的疾病,环境因素可能通过关键候选基因(如编码羧肽酶 A6 的 CPA6 基因)的表观遗传修饰发挥关键作用。因此,我们评估了 CPA6 启动子中的 DNA 甲基化。在 186 名 FE 患者和 92 名 FS 患者与 93 名健康对照和 42 名接受抗癫痫药物(AEDs)治疗的对照相比,我们发现癫痫患者的甲基化水平显著升高。FE 病例的甲基化状态为 3.4%(±3.2%),FS 病例为 4.3%(±3.5%),而健康个体和接受 AEDs 治疗的对照分别为 0.8%(±2.9%)和 1.5%(±3.9%)(所有比较的 p 值均≤0.001)。这些结果为 DNA 甲基化参与 FE 和 FS 提供了越来越多的证据。

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