Suppr超能文献

检测难治性癫痫患者脑脊液中的脑体细胞突变。

Detection of Brain Somatic Mutations in Cerebrospinal Fluid from Refractory Epilepsy Patients.

机构信息

Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.

Sorbonne University, Paris Brain Institute (ICM), National Institute of Health and Medical Research (INSERM), National Center for Scientific Research (CNRS), Paris, France.

出版信息

Ann Neurol. 2021 Jun;89(6):1248-1252. doi: 10.1002/ana.26080. Epub 2021 Apr 20.

Abstract

Brain mosaic mutations are a major cause of refractory focal epilepsies with cortical malformations such as focal cortical dysplasia, hemimegalencephaly, malformation of cortical development with oligodendroglial hyperplasia in epilepsy, and ganglioglioma. Here, we collected cerebrospinal fluid (CSF) during epilepsy surgery to search for somatic variants in cell-free DNA (cfDNA) using targeted droplet digital polymerase chain reaction. In 3 of 12 epileptic patients with known somatic mutations previously identified in brain tissue, we here provide evidence that brain mosaicism can be detected in the CSF-derived cfDNA. These findings suggest future opportunities for detecting the mutant allele driving epilepsy in CSF. ANN NEUROL 2021;89:1248-1252.

摘要

脑镶嵌突变是难治性局灶性癫痫的主要原因,其伴发皮质畸形,如局灶性皮质发育不良、偏侧巨脑畸形、伴巨细胞性胶质增生的皮质发育不良、节细胞胶质瘤等。在此,我们在癫痫手术期间收集脑脊液(CSF),使用靶向液滴数字聚合酶链反应(PCR)在无细胞 DNA(cfDNA)中寻找体细胞变异。在先前在脑组织中鉴定出已知体细胞突变的 12 名癫痫患者中的 3 名中,我们在此提供证据表明 CSF 衍生 cfDNA 中可检测到脑镶嵌现象。这些发现提示未来有机会在 CSF 中检测到驱动癫痫的突变等位基因。神经病学年鉴 2021;89:1248-1252.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验