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Automated lesion detection on MRI scans using combined unsupervised and supervised methods

BACKGROUND: Accurate and precise detection of brain lesions on MR images (MRI) is paramount for accurately relating lesion location to impaired behavior. In this paper, we present a novel method to automatically detect brain lesions from a T1-weighted 3D MRI. The proposed method combines the advanta...

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Autores principales: Guo, Dazhou, Fridriksson, Julius, Fillmore, Paul, Rorden, Christopher, Yu, Hongkai, Zheng, Kang, Wang, Song
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628334/
https://www.ncbi.nlm.nih.gov/pubmed/26518734
http://dx.doi.org/10.1186/s12880-015-0092-x
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author Guo, Dazhou
Fridriksson, Julius
Fillmore, Paul
Rorden, Christopher
Yu, Hongkai
Zheng, Kang
Wang, Song
author_facet Guo, Dazhou
Fridriksson, Julius
Fillmore, Paul
Rorden, Christopher
Yu, Hongkai
Zheng, Kang
Wang, Song
author_sort Guo, Dazhou
collection PubMed
description BACKGROUND: Accurate and precise detection of brain lesions on MR images (MRI) is paramount for accurately relating lesion location to impaired behavior. In this paper, we present a novel method to automatically detect brain lesions from a T1-weighted 3D MRI. The proposed method combines the advantages of both unsupervised and supervised methods. METHODS: First, unsupervised methods perform a unified segmentation normalization to warp images from the native space into a standard space and to generate probability maps for different tissue types, e.g., gray matter, white matter and fluid. This allows us to construct an initial lesion probability map by comparing the normalized MRI to healthy control subjects. Then, we perform non-rigid and reversible atlas-based registration to refine the probability maps of gray matter, white matter, external CSF, ventricle, and lesions. These probability maps are combined with the normalized MRI to construct three types of features, with which we use supervised methods to train three support vector machine (SVM) classifiers for a combined classifier. Finally, the combined classifier is used to accomplish lesion detection. RESULTS: We tested this method using T1-weighted MRIs from 60 in-house stroke patients. Using leave-one-out cross validation, the proposed method can achieve an average Dice coefficient of 73.1 % when compared to lesion maps hand-delineated by trained neurologists. Furthermore, we tested the proposed method on the T1-weighted MRIs in the MICCAI BRATS 2012 dataset. The proposed method can achieve an average Dice coefficient of 66.5 % in comparison to the expert annotated tumor maps provided in MICCAI BRATS 2012 dataset. In addition, on these two test datasets, the proposed method shows competitive performance to three state-of-the-art methods, including Stamatakis et al., Seghier et al., and Sanjuan et al. CONCLUSIONS: In this paper, we introduced a novel automated procedure for lesion detection from T1-weighted MRIs by combining both an unsupervised and a supervised component. In the unsupervised component, we proposed a method to identify lesioned hemisphere to help normalize the patient MRI with lesions and initialize/refine a lesion probability map. In the supervised component, we extracted three different-order statistical features from both the tissue/lesion probability maps obtained from the unsupervised component and the original MRI intensity. Three support vector machine classifiers are then trained for the three features respectively and combined for final voxel-based lesion classification.
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spelling pubmed-46283342015-11-01 Automated lesion detection on MRI scans using combined unsupervised and supervised methods Guo, Dazhou Fridriksson, Julius Fillmore, Paul Rorden, Christopher Yu, Hongkai Zheng, Kang Wang, Song BMC Med Imaging Research Article BACKGROUND: Accurate and precise detection of brain lesions on MR images (MRI) is paramount for accurately relating lesion location to impaired behavior. In this paper, we present a novel method to automatically detect brain lesions from a T1-weighted 3D MRI. The proposed method combines the advantages of both unsupervised and supervised methods. METHODS: First, unsupervised methods perform a unified segmentation normalization to warp images from the native space into a standard space and to generate probability maps for different tissue types, e.g., gray matter, white matter and fluid. This allows us to construct an initial lesion probability map by comparing the normalized MRI to healthy control subjects. Then, we perform non-rigid and reversible atlas-based registration to refine the probability maps of gray matter, white matter, external CSF, ventricle, and lesions. These probability maps are combined with the normalized MRI to construct three types of features, with which we use supervised methods to train three support vector machine (SVM) classifiers for a combined classifier. Finally, the combined classifier is used to accomplish lesion detection. RESULTS: We tested this method using T1-weighted MRIs from 60 in-house stroke patients. Using leave-one-out cross validation, the proposed method can achieve an average Dice coefficient of 73.1 % when compared to lesion maps hand-delineated by trained neurologists. Furthermore, we tested the proposed method on the T1-weighted MRIs in the MICCAI BRATS 2012 dataset. The proposed method can achieve an average Dice coefficient of 66.5 % in comparison to the expert annotated tumor maps provided in MICCAI BRATS 2012 dataset. In addition, on these two test datasets, the proposed method shows competitive performance to three state-of-the-art methods, including Stamatakis et al., Seghier et al., and Sanjuan et al. CONCLUSIONS: In this paper, we introduced a novel automated procedure for lesion detection from T1-weighted MRIs by combining both an unsupervised and a supervised component. In the unsupervised component, we proposed a method to identify lesioned hemisphere to help normalize the patient MRI with lesions and initialize/refine a lesion probability map. In the supervised component, we extracted three different-order statistical features from both the tissue/lesion probability maps obtained from the unsupervised component and the original MRI intensity. Three support vector machine classifiers are then trained for the three features respectively and combined for final voxel-based lesion classification. BioMed Central 2015-10-30 /pmc/articles/PMC4628334/ /pubmed/26518734 http://dx.doi.org/10.1186/s12880-015-0092-x Text en © Guo et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License(http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Guo, Dazhou
Fridriksson, Julius
Fillmore, Paul
Rorden, Christopher
Yu, Hongkai
Zheng, Kang
Wang, Song
Automated lesion detection on MRI scans using combined unsupervised and supervised methods
title Automated lesion detection on MRI scans using combined unsupervised and supervised methods
title_full Automated lesion detection on MRI scans using combined unsupervised and supervised methods
title_fullStr Automated lesion detection on MRI scans using combined unsupervised and supervised methods
title_full_unstemmed Automated lesion detection on MRI scans using combined unsupervised and supervised methods
title_short Automated lesion detection on MRI scans using combined unsupervised and supervised methods
title_sort automated lesion detection on mri scans using combined unsupervised and supervised methods
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628334/
https://www.ncbi.nlm.nih.gov/pubmed/26518734
http://dx.doi.org/10.1186/s12880-015-0092-x
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