Cargando…

Diffusion Tensor Imaging Reveals Microstructural Heterogeneity of Normal-Appearing White Matter and Related Cognitive Dysfunction in Glioma Patients

Immunohistochemical data based on isocitrate–dehydrogenase (IDH) mutation status have redefined glioma as a whole-brain disease, while occult tumor cell invasion along white matter fibers is inapparent in conventional magnetic resonance imaging (MRI). The functional and prognostic impact of focal gl...

Descripción completa

Detalles Bibliográficos
Autores principales: Jütten, Kerstin, Mainz, Verena, Gauggel, Siegfried, Patel, Harshal Jayeshkumar, Binkofski, Ferdinand, Wiesmann, Martin, Clusmann, Hans, Na, Chuh-Hyoun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6606770/
https://www.ncbi.nlm.nih.gov/pubmed/31293974
http://dx.doi.org/10.3389/fonc.2019.00536
_version_ 1783431965029957632
author Jütten, Kerstin
Mainz, Verena
Gauggel, Siegfried
Patel, Harshal Jayeshkumar
Binkofski, Ferdinand
Wiesmann, Martin
Clusmann, Hans
Na, Chuh-Hyoun
author_facet Jütten, Kerstin
Mainz, Verena
Gauggel, Siegfried
Patel, Harshal Jayeshkumar
Binkofski, Ferdinand
Wiesmann, Martin
Clusmann, Hans
Na, Chuh-Hyoun
author_sort Jütten, Kerstin
collection PubMed
description Immunohistochemical data based on isocitrate–dehydrogenase (IDH) mutation status have redefined glioma as a whole-brain disease, while occult tumor cell invasion along white matter fibers is inapparent in conventional magnetic resonance imaging (MRI). The functional and prognostic impact of focal glioma may however relate to the extent of white matter involvement. We used diffusion tensor imaging (DTI) to investigate microstructural characteristics of whole-brain normal-appearing white matter (NAWM) in relation to cognitive functions as potential surrogates for occult white matter involvement in glioma. Twenty patients (12 IDH-mutated) and 20 individually matched controls were preoperatively examined using DTI combined with a standardized neuropsychological examination. Tumor lesions including perifocal edema were masked, and fractional anisotropy (FA) as well as mean, radial, and axial diffusivity (MD, RD, and AD, respectively) of the remaining whole-brain NAWM were determined by using Tract-Based Spatial Statistics and histogram analyses. The relationship between extratumoral white matter integrity and cognitive performance was examined using partial correlation analyses controlling for age, education, and lesion volumes. In patients, mean FA and AD were decreased as compared to controls, which agrees with the notion of microstructural impairment of NAWM in glioma patients. Patients performed worse in all cognitive domains tested, and higher anisotropy and lower MD and RD values of NAWM were associated with better cognitive performance. In additional analyses, IDH-mutated and IDH-wildtype patients were compared. Patients with IDH-mutation showed higher FA, but lower MD, AD, and RD values as compared to IDH-wildtype patients, suggesting a better preserved microstructural integrity of NAWM, which may relate to a less infiltrative nature of IDH-mutated gliomas. Diffusion-based phenotyping and monitoring microstructural integrity of extratumoral whole-brain NAWM may aid in estimating occult white matter involvement and should be considered as a complementary biomarker in glioma.
format Online
Article
Text
id pubmed-6606770
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-66067702019-07-10 Diffusion Tensor Imaging Reveals Microstructural Heterogeneity of Normal-Appearing White Matter and Related Cognitive Dysfunction in Glioma Patients Jütten, Kerstin Mainz, Verena Gauggel, Siegfried Patel, Harshal Jayeshkumar Binkofski, Ferdinand Wiesmann, Martin Clusmann, Hans Na, Chuh-Hyoun Front Oncol Oncology Immunohistochemical data based on isocitrate–dehydrogenase (IDH) mutation status have redefined glioma as a whole-brain disease, while occult tumor cell invasion along white matter fibers is inapparent in conventional magnetic resonance imaging (MRI). The functional and prognostic impact of focal glioma may however relate to the extent of white matter involvement. We used diffusion tensor imaging (DTI) to investigate microstructural characteristics of whole-brain normal-appearing white matter (NAWM) in relation to cognitive functions as potential surrogates for occult white matter involvement in glioma. Twenty patients (12 IDH-mutated) and 20 individually matched controls were preoperatively examined using DTI combined with a standardized neuropsychological examination. Tumor lesions including perifocal edema were masked, and fractional anisotropy (FA) as well as mean, radial, and axial diffusivity (MD, RD, and AD, respectively) of the remaining whole-brain NAWM were determined by using Tract-Based Spatial Statistics and histogram analyses. The relationship between extratumoral white matter integrity and cognitive performance was examined using partial correlation analyses controlling for age, education, and lesion volumes. In patients, mean FA and AD were decreased as compared to controls, which agrees with the notion of microstructural impairment of NAWM in glioma patients. Patients performed worse in all cognitive domains tested, and higher anisotropy and lower MD and RD values of NAWM were associated with better cognitive performance. In additional analyses, IDH-mutated and IDH-wildtype patients were compared. Patients with IDH-mutation showed higher FA, but lower MD, AD, and RD values as compared to IDH-wildtype patients, suggesting a better preserved microstructural integrity of NAWM, which may relate to a less infiltrative nature of IDH-mutated gliomas. Diffusion-based phenotyping and monitoring microstructural integrity of extratumoral whole-brain NAWM may aid in estimating occult white matter involvement and should be considered as a complementary biomarker in glioma. Frontiers Media S.A. 2019-06-26 /pmc/articles/PMC6606770/ /pubmed/31293974 http://dx.doi.org/10.3389/fonc.2019.00536 Text en Copyright © 2019 Jütten, Mainz, Gauggel, Patel, Binkofski, Wiesmann, Clusmann and Na. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Jütten, Kerstin
Mainz, Verena
Gauggel, Siegfried
Patel, Harshal Jayeshkumar
Binkofski, Ferdinand
Wiesmann, Martin
Clusmann, Hans
Na, Chuh-Hyoun
Diffusion Tensor Imaging Reveals Microstructural Heterogeneity of Normal-Appearing White Matter and Related Cognitive Dysfunction in Glioma Patients
title Diffusion Tensor Imaging Reveals Microstructural Heterogeneity of Normal-Appearing White Matter and Related Cognitive Dysfunction in Glioma Patients
title_full Diffusion Tensor Imaging Reveals Microstructural Heterogeneity of Normal-Appearing White Matter and Related Cognitive Dysfunction in Glioma Patients
title_fullStr Diffusion Tensor Imaging Reveals Microstructural Heterogeneity of Normal-Appearing White Matter and Related Cognitive Dysfunction in Glioma Patients
title_full_unstemmed Diffusion Tensor Imaging Reveals Microstructural Heterogeneity of Normal-Appearing White Matter and Related Cognitive Dysfunction in Glioma Patients
title_short Diffusion Tensor Imaging Reveals Microstructural Heterogeneity of Normal-Appearing White Matter and Related Cognitive Dysfunction in Glioma Patients
title_sort diffusion tensor imaging reveals microstructural heterogeneity of normal-appearing white matter and related cognitive dysfunction in glioma patients
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6606770/
https://www.ncbi.nlm.nih.gov/pubmed/31293974
http://dx.doi.org/10.3389/fonc.2019.00536
work_keys_str_mv AT juttenkerstin diffusiontensorimagingrevealsmicrostructuralheterogeneityofnormalappearingwhitematterandrelatedcognitivedysfunctioningliomapatients
AT mainzverena diffusiontensorimagingrevealsmicrostructuralheterogeneityofnormalappearingwhitematterandrelatedcognitivedysfunctioningliomapatients
AT gauggelsiegfried diffusiontensorimagingrevealsmicrostructuralheterogeneityofnormalappearingwhitematterandrelatedcognitivedysfunctioningliomapatients
AT patelharshaljayeshkumar diffusiontensorimagingrevealsmicrostructuralheterogeneityofnormalappearingwhitematterandrelatedcognitivedysfunctioningliomapatients
AT binkofskiferdinand diffusiontensorimagingrevealsmicrostructuralheterogeneityofnormalappearingwhitematterandrelatedcognitivedysfunctioningliomapatients
AT wiesmannmartin diffusiontensorimagingrevealsmicrostructuralheterogeneityofnormalappearingwhitematterandrelatedcognitivedysfunctioningliomapatients
AT clusmannhans diffusiontensorimagingrevealsmicrostructuralheterogeneityofnormalappearingwhitematterandrelatedcognitivedysfunctioningliomapatients
AT nachuhhyoun diffusiontensorimagingrevealsmicrostructuralheterogeneityofnormalappearingwhitematterandrelatedcognitivedysfunctioningliomapatients