Chen Y, Bao X H, Zhang Q P, Wang J P, Wen Y X, Yu S J, Zhao Y
Department of Pediatrics, Peking University First Hospital, Beijing 100034, China.
Zhonghua Er Ke Za Zhi. 2018 Nov 2;56(11):824-828. doi: 10.3760/cma.j.issn.0578-1310.2018.11.007.
To study the mutational characteristics of KCNT1 and its clinical features in children with early-onset epileptic encephalopathy. Retrospective analysis of clinical data of 175 children with early onset epilepsy from the Department of Pediatrics at Peking University First Hospital from January 2012 to December 2017. Gene-based analysis was performed on children with targeted capture second-generation sequencing and the source of mutations was verified by PCR-Sanger. The clinical features of children with KCNT1 mutation were summarized. In 175 infants with early-onset epileptic encephalopathy, 6 children were found to have KCNT1 mutations, all of which were new mutations with an overall mutation rate of 3.4% (6/175). All the mutations were missense mutations. The age of onset was from 2 days to 32 days. Five children were diagnosed with epilepsy of infancy with migrating focal seizure, one case was diagnosed with epilepsy, focal seizures, focal seizures with generalization. A total of 6 children were treated with multi-antiepileptic drugs. The disease in 4 patients were partially controlled, while in 2 patients, the disease was not significantly alleviated. One patient died of "severe pneumonia" at one year and 4 months of age. Then, four cases were treated with quinidine. The seizure frequency had no change in 3 cases, the frequency decreased and then relapsed in 1 case. The case once ketogenic diet and failed. Ketogenic diet treatment was applied to 5 cases, no significant effect was achieved. All the 6 patients had severe developmental delay. They could not sit alone, follow the light and objects and had no language. The mutation of KCNT1 gene is mainly de novo. The onset of the disease was early, and mostly occurs in neonate and early infancy. The main seizure type was epilepsy of infancy with migrating focal seizure. Patients usually had severe psychomotor developmental delay. Antiepileptic drugs are ineffective. The efficacy of quinidine was not significant. Though, it still need studies on a large sample.
研究KCNT1基因在早发性癫痫性脑病患儿中的突变特征及其临床特点。回顾性分析2012年1月至2017年12月北京大学第一医院儿科175例早发性癫痫患儿的临床资料。对患儿进行靶向捕获二代测序的基因分析,并通过PCR-Sanger法验证突变来源。总结KCNT1基因突变患儿的临床特征。在175例早发性癫痫性脑病婴儿中,发现6例患儿存在KCNT1基因突变,均为新发突变,总体突变率为3.4%(6/175)。所有突变均为错义突变。发病年龄为2天至32天。5例患儿诊断为婴儿游走性局灶性癫痫发作,1例诊断为癫痫、局灶性发作、局灶性发作继发全面性发作。6例患儿均接受多种抗癫痫药物治疗。4例患儿病情部分得到控制,2例患儿病情无明显缓解。1例患儿在1岁4个月时死于“重症肺炎”。之后,4例患儿接受奎尼丁治疗。3例患儿癫痫发作频率无变化,1例患儿发作频率先降低后复发。该患儿曾进行生酮饮食治疗但失败。5例患儿接受生酮饮食治疗,未取得明显效果。6例患儿均有严重发育迟缓。不能独坐、追光追物,无语言能力。KCNT1基因突变主要为新发突变。起病早,多发生于新生儿及婴儿早期。主要发作类型为婴儿游走性局灶性癫痫发作。患者通常有严重的精神运动发育迟缓。抗癫痫药物治疗无效。奎尼丁疗效不显著。不过,仍需大样本研究。