Magnetic resonance diffusion-tensor imaging metrics in High Grade Gliomas: Correlation with IDH1 gene status in WHO 2016 era

Eur J Radiol. 2019 Jul:116:174-179. doi: 10.1016/j.ejrad.2019.04.020. Epub 2019 May 7.

Abstract

Purpose: To evaluate any possible correlation between the presence of Isocitrate DeHydrogenase 1 mutation (IDH1m) and specific DTI (Diffusion Tensor Imaging) metrics, such as Fractional Anisotropy (FA), Mean Diffusivity (MD), Radial Diffusivity (RD) and Axial Diffusivity (AD).

Methods: We retrospectively analyzed 47 patients who underwent an advanced-MR study with DTI followed by surgical intervention with a subsequent histologic diagnosis of High-Grade Glioma (HGG) and immunohistochemical evaluation of IDH1 (Isocitrate DeHydrogenase) mutation status. For each DTI metrics we measured the ratio between tumor and normal tissue and we evaluated the correlation with IDH1 mutation.

Results: We observed a positive correlation with IDH1 status and RD and MD data. No correlation was demonstrated between IDH1 status and FA and AD.

Discussion: Our results support the hypothesis that the number of residual axonal fibers, extracellular matrix composition and the presence of colliquated tissue, may together contribute to a global RD increase in HGG, with a relatively higher increase in IDH1m tumors.

Conclusions: Our data are in favor of a need for multimodal advance evaluation of HGG. DTI metrics help to analyze IDH1 mutation status, in order to better characterize the lesions and to tailor treatment and follow up.

Keywords: Diffusion tensor imaging metrics; Fractional anisotropy; High-Grade Glioma; Isocitrate DeHydrogenase mutation; Radial diffusivity; WHO glioma classification.

Publication types

  • Evaluation Study

MeSH terms

  • Adult
  • Aged
  • Anisotropy
  • Diffusion Tensor Imaging / methods
  • Female
  • Glioma / genetics
  • Glioma / pathology*
  • Humans
  • Isocitrate Dehydrogenase / genetics*
  • Magnetic Resonance Spectroscopy
  • Male
  • Middle Aged
  • Multimodal Imaging
  • Mutation / genetics*
  • Retrospective Studies

Substances

  • Isocitrate Dehydrogenase
  • IDH1 protein, human