Microvasculature Features Derived from Hybrid EPI MRI in Non-Enhancing Adult-Type Diffuse Glioma Subtypes

Author:

Arzanforoosh Fatemeh12ORCID,van der Voort Sebastian R.12,Incekara Fatih13,Vincent Arnaud23,Van den Bent Martin24ORCID,Kros Johan M.25ORCID,Smits Marion126,Warnert Esther A. H.12

Affiliation:

1. Department of Radiology and Nuclear Medicine, Erasmus MC, 3015 GD Rotterdam, The Netherlands

2. Brain Tumor Center, Erasmus MC Cancer Institute, 3015 GD Rotterdam, The Netherlands

3. Department of Neurosurgery, Erasmus MC, 3015 GD Rotterdam, The Netherlands

4. Department of Neurology, Erasmus MC, 3015 GD Rotterdam, The Netherlands

5. Department of Pathology, Erasmus MC, 3000 CB Rotterdam, The Netherlands

6. Medical Delta, 2629 JH Delft, The Netherlands

Abstract

In this study, we used the vessel size imaging (VSI) MRI technique to characterize the microvasculature features of three subtypes of adult-type diffuse glioma lacking enhancement. Thirty-eight patients with confirmed non-enhancing glioma were categorized into three subtypes: Oligo (IDH-mut&1p/19q-codeleted), Astro (IDH-mut), and GBM (IDH-wt). The VSI technique provided quantitative maps of cerebral blood volume (CBV), microvasculature (µCBV), and vessel size for each patient. Additionally, tissue samples of 21 patients were histopathologically analyzed, and microvasculature features were quantified. Both MRI- and histology-derived features were compared across the three glioma subtypes with ANOVA or Kruskal–Wallis tests. Group averages of CBV, μCBV, and vessel size were significantly different between the three glioma subtypes (p < 0.01). Astro (IDH-mut) had a significantly lower CBV and µCBV compared to Oligo (IDH-mut&1p/19q-codeleted) (p = 0.004 and p = 0.001, respectively), and a higher average vessel size compared to GBM (IDH-wt) (p = 0.01). The histopathological analysis showed that GBM (IDH-wt) possessed vessels with more irregular shapes than the two other subtypes (p < 0.05). VSI provides a good insight into the microvasculature characteristics of the three adult-type glioma subtypes even when lacking enhancement. Further investigations into the specificity of VSI to differentiate glioma subtypes are thus warranted.

Funder

Dutch Cancer Society

Veni Vernieuwingsimpuls

Dutch Research Council

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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