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Tissue-type mapping of gliomas

PURPOSE: To develop a statistical method of combining multimodal MRI (mMRI) of adult glial brain tumours to generate tissue heterogeneity maps that indicate tumour grade and infiltration margins. MATERIALS AND METHODS: We performed a retrospective analysis of mMRI from patients with histological dia...

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Autores principales: Raschke, Felix, Barrick, Thomas R., Jones, Timothy L., Yang, Guang, Ye, Xujiong, Howe, Franklyn A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411966/
https://www.ncbi.nlm.nih.gov/pubmed/30630760
http://dx.doi.org/10.1016/j.nicl.2018.101648
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author Raschke, Felix
Barrick, Thomas R.
Jones, Timothy L.
Yang, Guang
Ye, Xujiong
Howe, Franklyn A.
author_facet Raschke, Felix
Barrick, Thomas R.
Jones, Timothy L.
Yang, Guang
Ye, Xujiong
Howe, Franklyn A.
author_sort Raschke, Felix
collection PubMed
description PURPOSE: To develop a statistical method of combining multimodal MRI (mMRI) of adult glial brain tumours to generate tissue heterogeneity maps that indicate tumour grade and infiltration margins. MATERIALS AND METHODS: We performed a retrospective analysis of mMRI from patients with histological diagnosis of glioma (n = 25). (1)H Magnetic Resonance Spectroscopic Imaging (MRSI) was used to label regions of “pure” low- or high-grade tumour across image types. Normal brain and oedema characteristics were defined from healthy controls (n = 10) and brain metastasis patients (n = 10) respectively. Probability density distributions (PDD) for each tissue type were extracted from intensity normalised proton density and T(2)-weighted images, and p and q diffusion maps. Superpixel segmentation and Bayesian inference was used to produce whole-brain tissue-type maps. RESULTS: Total lesion volumes derived automatically from tissue-type maps correlated with those from manual delineation (p < 0.001, r = 0.87). Large high-grade volumes were determined in all grade III & IV (n = 16) tumours, in grade II gemistocytic rich astrocytomas (n = 3) and one astrocytoma with a histological diagnosis of grade II. For patients with known outcome (n = 20), patients with survival time < 2 years (3 grade II, 2 grade III and 10 grade IV) had a high-grade volume significantly greater than zero (Wilcoxon signed rank p < 0.0001) and also significantly greater high grade volume than the 5 grade II patients with survival >2 years (Mann Witney p = 0.0001). Regions classified from mMRI as oedema had non-tumour-like (1)H MRS characteristics. CONCLUSIONS: (1)H MRSI can label tumour tissue types to enable development of a mMRI tissue type mapping algorithm, with potential to aid management of patients with glial tumours.
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spelling pubmed-64119662019-03-22 Tissue-type mapping of gliomas Raschke, Felix Barrick, Thomas R. Jones, Timothy L. Yang, Guang Ye, Xujiong Howe, Franklyn A. Neuroimage Clin Article PURPOSE: To develop a statistical method of combining multimodal MRI (mMRI) of adult glial brain tumours to generate tissue heterogeneity maps that indicate tumour grade and infiltration margins. MATERIALS AND METHODS: We performed a retrospective analysis of mMRI from patients with histological diagnosis of glioma (n = 25). (1)H Magnetic Resonance Spectroscopic Imaging (MRSI) was used to label regions of “pure” low- or high-grade tumour across image types. Normal brain and oedema characteristics were defined from healthy controls (n = 10) and brain metastasis patients (n = 10) respectively. Probability density distributions (PDD) for each tissue type were extracted from intensity normalised proton density and T(2)-weighted images, and p and q diffusion maps. Superpixel segmentation and Bayesian inference was used to produce whole-brain tissue-type maps. RESULTS: Total lesion volumes derived automatically from tissue-type maps correlated with those from manual delineation (p < 0.001, r = 0.87). Large high-grade volumes were determined in all grade III & IV (n = 16) tumours, in grade II gemistocytic rich astrocytomas (n = 3) and one astrocytoma with a histological diagnosis of grade II. For patients with known outcome (n = 20), patients with survival time < 2 years (3 grade II, 2 grade III and 10 grade IV) had a high-grade volume significantly greater than zero (Wilcoxon signed rank p < 0.0001) and also significantly greater high grade volume than the 5 grade II patients with survival >2 years (Mann Witney p = 0.0001). Regions classified from mMRI as oedema had non-tumour-like (1)H MRS characteristics. CONCLUSIONS: (1)H MRSI can label tumour tissue types to enable development of a mMRI tissue type mapping algorithm, with potential to aid management of patients with glial tumours. Elsevier 2018-12-25 /pmc/articles/PMC6411966/ /pubmed/30630760 http://dx.doi.org/10.1016/j.nicl.2018.101648 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Raschke, Felix
Barrick, Thomas R.
Jones, Timothy L.
Yang, Guang
Ye, Xujiong
Howe, Franklyn A.
Tissue-type mapping of gliomas
title Tissue-type mapping of gliomas
title_full Tissue-type mapping of gliomas
title_fullStr Tissue-type mapping of gliomas
title_full_unstemmed Tissue-type mapping of gliomas
title_short Tissue-type mapping of gliomas
title_sort tissue-type mapping of gliomas
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411966/
https://www.ncbi.nlm.nih.gov/pubmed/30630760
http://dx.doi.org/10.1016/j.nicl.2018.101648
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