国家神经系统疾病临床医学研究中心数据管理与共享系统

Data Management And Sharing System of China National Clinical Research Center for Neurological Diseases

IDH1/2 mutation is associated with seizure as an initial symptom in low-grade glioma:A report of 311 Chinese adult glioma patients

第一作者:Zhang Zhong

通讯作者:Tao Jiang

IDH1/2 mutation glioma

基本信息

  • 负责人:Zhang Zhong
  • 数据来源: OTHERS
  • 论文编号:OTHERS20190336
  • 发表时间:2015-01-01

2015-01-01

已发表文章

发表杂志:Epilepsy Research

发表类型: Research Article

影响因子(IF): 3.045

PMID: 25524848 Pubmed原文链接 全文下载

主要研究背景及目的

方法

A total of 311 adult patients with LGG were enrolled in our study with both clinical data and IDH1/2 mutation data available. IDH1/2 mutation was detected directly by pyro-sequencing. The chi-squared test was performed to determine whether the IDH1/2 mutation has any relevance to seizure onset and to evaluate the potential impact that IDH1/2 mutation may exert on seizure control postoperatively.

结论

IDH1/2 mutation occurs more frequently in LGG patients with seizure as an initial symptom, suggesting a potential relationship between this genetic phenotype and clinical seizure presentation. IDH1/2 mutation shows no prognostic value for postoperative seizure control.

主要结果

Seizure presented as an initial symptom in 71.4% (222/311) of patients with LGG, among which 189 patients were detected to bear IDH1/2 mutation in their tumors (P=0.035, chi-squared test). However, IDH1/2 mutation does not seem to contribute to the seizure control postoperatively (P=0.350 and 0.577 for the 6- and 12-month follow-up, respectively, chi-squared test).