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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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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. |
format | Online Article Text |
id | pubmed-6411966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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