Correlation of Clinicopathological Factors with Brain Tumor-Related Epilepsy in Glioma

Dis Markers. 2022 Sep 30:2022:4918294. doi: 10.1155/2022/4918294. eCollection 2022.

Abstract

Objectives: Glioma patients with brain tumor-related epilepsy (BTRE) have a complex profile due to the simultaneous presence of two pathologies, glioma and epilepsy; however, they have not traditionally received as much attention as those with more malignant brain tumors. The underlying pathophysiology of brain tumor-related epilepsy remains poorly understood. The purpose of this study was to investigate the possible correlation between molecular neuropathology and glioma with BTRE and a wide range of BTRE-associated molecular markers of glioma patients.

Methods: A retrospective cohort study of 186 glioma patients was evaluated at our hospital, of which 64 had BTRE. The chi-square test, Spearman rank correlation, and multivariate logistic analyses were used to identify clinicopathological factors associated with BTRE in glioma patients.

Results: Of the 186 patients examined in this study, 64 (34.4%) had BTRE. Based on the analysis of the characteristics of these patients, the results showed that patient age (over 40 years; P = 0.007), low WHO grade (grade I, II; P = 0.001), IDH-1 positive mutation (P = 0.027), low ATR-X expression level (OR = 0.44; 95% CI: 0.21, 0.92), and low Ki-67 PI (OR = 0.25; 95% CI: 0.10, 0.68) were associated with the occurrence of BTRE. In our cohort, BTRE patients did not differ by sex, tumor location, or expression of olig-2 and CD34. The results of the matching study showed that low Ki-67 PI and negative ATR-X expression levels were independent factors for a higher incidence of preoperative seizures in glioma patients.

Conclusion: The current study updates existing information on genetic markers in gliomas with BTRE and explores the correlation of a wide range of clinicopathological factors and glioma patients with BTRE and suggests three putative biomarkers for BTRE: positive IDH1 mutation, low Ki-67 PI, and negative ATR-X expression. These factors may provide insights for developing a more thorough understanding of the pathogenesis of epilepsy and effective treatment strategies aimed at seizure control.

Publication types

  • Retracted Publication

MeSH terms

  • Adult
  • Brain Neoplasms* / complications
  • Brain Neoplasms* / genetics
  • Brain Neoplasms* / pathology
  • Epilepsy* / complications
  • Epilepsy* / genetics
  • Genetic Markers
  • Glioma* / complications
  • Glioma* / genetics
  • Glioma* / pathology
  • Humans
  • Ki-67 Antigen / genetics
  • Retrospective Studies
  • Seizures / etiology

Substances

  • Genetic Markers
  • Ki-67 Antigen