Association of preoperative seizures with tumor metabolites quantified by magnetic resonance spectroscopy in gliomas

Sci Rep. 2021 Apr 12;11(1):7927. doi: 10.1038/s41598-021-86487-6.

Abstract

Seizures are common in patients with gliomas; however, the mechanisms of epileptogenesis in gliomas have not been fully understood. This study hypothesized that analyzing quantified metabolites using magnetic resonance spectroscopy (MRS) might provide novel insights to better understand the epileptogenesis in gliomas, and specific metabolites might be indicators of preoperative seizures in gliomas. We retrospectively investigated patient information (gender, age at diagnosis of tumor, their survival time) and tumor information (location, histology, genetic features, and metabolites according to MRS) in patients with gliomas. The data were correlated with the incidence of seizure and analyzed statistically. Of 146 adult supratentorial gliomas, isocitrate dehydrogenase (IDH) mutant tumors significantly indicated higher incidence of preoperative seizures than IDH wild-type gliomas. However, MRS study indicated that glutamate concentration in IDH wild-type gliomas was higher than that in IDH mutant gliomas. Glutamate was not associated with high frequency of preoperative seizures in patients with gliomas. Instead, increased total N-acetyl-L-aspartate (tNAA) was significantly associated with them. Moreover, multivariable analysis indicated that increased level of tNAA was an independent predictor of preoperative seizures. According to MRS analysis, tNAA, rather than glutamate, might be a useful to detect preoperative seizures in patient with supratentorial gliomas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Aspartic Acid / analogs & derivatives
  • Aspartic Acid / metabolism
  • Astrocytes / pathology
  • Brain Neoplasms / diagnostic imaging
  • Brain Neoplasms / metabolism*
  • Brain Neoplasms / surgery*
  • Female
  • Glioma / diagnostic imaging
  • Glioma / metabolism*
  • Glioma / surgery*
  • Glutamic Acid / metabolism
  • Humans
  • Isocitrate Dehydrogenase / genetics
  • Magnetic Resonance Spectroscopy*
  • Male
  • Metabolome*
  • Middle Aged
  • Multivariate Analysis
  • Mutation / genetics
  • Oligodendroglia / pathology
  • Seizures / complications*
  • Seizures / diagnostic imaging
  • Survival Analysis
  • Young Adult

Substances

  • Aspartic Acid
  • Glutamic Acid
  • N-acetylaspartate
  • Isocitrate Dehydrogenase