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Texture Analysis of T2-Weighted MR Images to Assess Acute Inflammation in Brain MS Lesions

Brain blood barrier breakdown as assessed by contrast-enhanced (CE) T1-weighted MR imaging is currently the standard radiological marker of inflammatory activity in multiple sclerosis (MS) patients. Our objective was to evaluate the performance of an alternative model assessing the inflammatory acti...

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Autores principales: Michoux, Nicolas, Guillet, Alain, Rommel, Denis, Mazzamuto, Giosué, Sindic, Christian, Duprez, Thierry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687842/
https://www.ncbi.nlm.nih.gov/pubmed/26693908
http://dx.doi.org/10.1371/journal.pone.0145497
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author Michoux, Nicolas
Guillet, Alain
Rommel, Denis
Mazzamuto, Giosué
Sindic, Christian
Duprez, Thierry
author_facet Michoux, Nicolas
Guillet, Alain
Rommel, Denis
Mazzamuto, Giosué
Sindic, Christian
Duprez, Thierry
author_sort Michoux, Nicolas
collection PubMed
description Brain blood barrier breakdown as assessed by contrast-enhanced (CE) T1-weighted MR imaging is currently the standard radiological marker of inflammatory activity in multiple sclerosis (MS) patients. Our objective was to evaluate the performance of an alternative model assessing the inflammatory activity of MS lesions by texture analysis of T2-weighted MR images. Twenty-one patients with definite MS were examined on the same 3.0T MR system by T2-weighted, FLAIR, diffusion-weighted and CE-T1 sequences. Lesions and mirrored contralateral areas within the normal appearing white matter (NAWM) were characterized by texture parameters computed from the gray level co-occurrence and run length matrices, and by the apparent diffusion coefficient (ADC). Statistical differences between MS lesions and NAWM were analyzed. ROC analysis and leave-one-out cross-validation were performed to evaluate the performance of individual parameters, and multi-parametric models using linear discriminant analysis (LDA), partial least squares (PLS) and logistic regression (LR) in the identification of CE lesions. ADC and all but one texture parameter were significantly different within white matter lesions compared to within NAWM (p < 0.0167). Using LDA, an 8-texture parameter model identified CE lesions with a sensitivity Se = 70% and a specificity Sp = 76%. Using LR, a 10-texture parameter model performed better with Se = 86% / Sp = 84%. Using PLS, a 6-texture parameter model achieved the highest accuracy with Se = 88% / Sp = 81%. Texture parameter from T2-weighted images can assess brain inflammatory activity with sufficient accuracy to be considered as a potential alternative to enhancement on CE T1-weighted images.
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spelling pubmed-46878422015-12-31 Texture Analysis of T2-Weighted MR Images to Assess Acute Inflammation in Brain MS Lesions Michoux, Nicolas Guillet, Alain Rommel, Denis Mazzamuto, Giosué Sindic, Christian Duprez, Thierry PLoS One Research Article Brain blood barrier breakdown as assessed by contrast-enhanced (CE) T1-weighted MR imaging is currently the standard radiological marker of inflammatory activity in multiple sclerosis (MS) patients. Our objective was to evaluate the performance of an alternative model assessing the inflammatory activity of MS lesions by texture analysis of T2-weighted MR images. Twenty-one patients with definite MS were examined on the same 3.0T MR system by T2-weighted, FLAIR, diffusion-weighted and CE-T1 sequences. Lesions and mirrored contralateral areas within the normal appearing white matter (NAWM) were characterized by texture parameters computed from the gray level co-occurrence and run length matrices, and by the apparent diffusion coefficient (ADC). Statistical differences between MS lesions and NAWM were analyzed. ROC analysis and leave-one-out cross-validation were performed to evaluate the performance of individual parameters, and multi-parametric models using linear discriminant analysis (LDA), partial least squares (PLS) and logistic regression (LR) in the identification of CE lesions. ADC and all but one texture parameter were significantly different within white matter lesions compared to within NAWM (p < 0.0167). Using LDA, an 8-texture parameter model identified CE lesions with a sensitivity Se = 70% and a specificity Sp = 76%. Using LR, a 10-texture parameter model performed better with Se = 86% / Sp = 84%. Using PLS, a 6-texture parameter model achieved the highest accuracy with Se = 88% / Sp = 81%. Texture parameter from T2-weighted images can assess brain inflammatory activity with sufficient accuracy to be considered as a potential alternative to enhancement on CE T1-weighted images. Public Library of Science 2015-12-22 /pmc/articles/PMC4687842/ /pubmed/26693908 http://dx.doi.org/10.1371/journal.pone.0145497 Text en © 2015 Michoux et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Michoux, Nicolas
Guillet, Alain
Rommel, Denis
Mazzamuto, Giosué
Sindic, Christian
Duprez, Thierry
Texture Analysis of T2-Weighted MR Images to Assess Acute Inflammation in Brain MS Lesions
title Texture Analysis of T2-Weighted MR Images to Assess Acute Inflammation in Brain MS Lesions
title_full Texture Analysis of T2-Weighted MR Images to Assess Acute Inflammation in Brain MS Lesions
title_fullStr Texture Analysis of T2-Weighted MR Images to Assess Acute Inflammation in Brain MS Lesions
title_full_unstemmed Texture Analysis of T2-Weighted MR Images to Assess Acute Inflammation in Brain MS Lesions
title_short Texture Analysis of T2-Weighted MR Images to Assess Acute Inflammation in Brain MS Lesions
title_sort texture analysis of t2-weighted mr images to assess acute inflammation in brain ms lesions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687842/
https://www.ncbi.nlm.nih.gov/pubmed/26693908
http://dx.doi.org/10.1371/journal.pone.0145497
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