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Fully automated longitudinal segmentation of new or enlarged multiple sclerosis lesions using 3D convolutional neural networks

The quantification of new or enlarged lesions from follow-up MRI scans is an important surrogate of clinical disease activity in patients with multiple sclerosis (MS). Not only is manual segmentation time consuming, but inter-rater variability is high. Currently, only a few fully automated methods a...

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Autores principales: Krüger, Julia, Opfer, Roland, Gessert, Nils, Ostwaldt, Ann-Christin, Manogaran, Praveena, Kitzler, Hagen H., Schlaefer, Alexander, Schippling, Sven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7554211/
https://www.ncbi.nlm.nih.gov/pubmed/33038667
http://dx.doi.org/10.1016/j.nicl.2020.102445
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author Krüger, Julia
Opfer, Roland
Gessert, Nils
Ostwaldt, Ann-Christin
Manogaran, Praveena
Kitzler, Hagen H.
Schlaefer, Alexander
Schippling, Sven
author_facet Krüger, Julia
Opfer, Roland
Gessert, Nils
Ostwaldt, Ann-Christin
Manogaran, Praveena
Kitzler, Hagen H.
Schlaefer, Alexander
Schippling, Sven
author_sort Krüger, Julia
collection PubMed
description The quantification of new or enlarged lesions from follow-up MRI scans is an important surrogate of clinical disease activity in patients with multiple sclerosis (MS). Not only is manual segmentation time consuming, but inter-rater variability is high. Currently, only a few fully automated methods are available. We address this gap in the field by employing a 3D convolutional neural network (CNN) with encoder-decoder architecture for fully automatic longitudinal lesion segmentation. Input data consist of two fluid attenuated inversion recovery (FLAIR) images (baseline and follow-up) per patient. Each image is entered into the encoder and the feature maps are concatenated and then fed into the decoder. The output is a 3D mask indicating new or enlarged lesions (compared to the baseline scan). The proposed method was trained on 1809 single point and 1444 longitudinal patient data sets and then validated on 185 independent longitudinal data sets from two different scanners. From the two validation data sets, manual segmentations were available from three experienced raters, respectively. The performance of the proposed method was compared to the open source Lesion Segmentation Toolbox (LST), which is a current state-of-art longitudinal lesion segmentation method. The mean lesion-wise inter-rater sensitivity was 62%, while the mean inter-rater number of false positive (FP) findings was 0.41 lesions per case. The two validated algorithms showed a mean sensitivity of 60% (CNN), 46% (LST) and a mean FP of 0.48 (CNN), 1.86 (LST) per case. Sensitivity and number of FP were not significantly different (p < 0.05) between the CNN and manual raters. New or enlarged lesions counted by the CNN algorithm appeared to be comparable with manual expert ratings. The proposed algorithm seems to outperform currently available approaches, particularly LST. The high inter-rater variability in case of manual segmentation indicates the complexity of identifying new or enlarged lesions. An automated CNN-based approach can quickly provide an independent and deterministic assessment of new or enlarged lesions from baseline to follow-up scans with acceptable reliability.
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spelling pubmed-75542112020-10-19 Fully automated longitudinal segmentation of new or enlarged multiple sclerosis lesions using 3D convolutional neural networks Krüger, Julia Opfer, Roland Gessert, Nils Ostwaldt, Ann-Christin Manogaran, Praveena Kitzler, Hagen H. Schlaefer, Alexander Schippling, Sven Neuroimage Clin Regular Article The quantification of new or enlarged lesions from follow-up MRI scans is an important surrogate of clinical disease activity in patients with multiple sclerosis (MS). Not only is manual segmentation time consuming, but inter-rater variability is high. Currently, only a few fully automated methods are available. We address this gap in the field by employing a 3D convolutional neural network (CNN) with encoder-decoder architecture for fully automatic longitudinal lesion segmentation. Input data consist of two fluid attenuated inversion recovery (FLAIR) images (baseline and follow-up) per patient. Each image is entered into the encoder and the feature maps are concatenated and then fed into the decoder. The output is a 3D mask indicating new or enlarged lesions (compared to the baseline scan). The proposed method was trained on 1809 single point and 1444 longitudinal patient data sets and then validated on 185 independent longitudinal data sets from two different scanners. From the two validation data sets, manual segmentations were available from three experienced raters, respectively. The performance of the proposed method was compared to the open source Lesion Segmentation Toolbox (LST), which is a current state-of-art longitudinal lesion segmentation method. The mean lesion-wise inter-rater sensitivity was 62%, while the mean inter-rater number of false positive (FP) findings was 0.41 lesions per case. The two validated algorithms showed a mean sensitivity of 60% (CNN), 46% (LST) and a mean FP of 0.48 (CNN), 1.86 (LST) per case. Sensitivity and number of FP were not significantly different (p < 0.05) between the CNN and manual raters. New or enlarged lesions counted by the CNN algorithm appeared to be comparable with manual expert ratings. The proposed algorithm seems to outperform currently available approaches, particularly LST. The high inter-rater variability in case of manual segmentation indicates the complexity of identifying new or enlarged lesions. An automated CNN-based approach can quickly provide an independent and deterministic assessment of new or enlarged lesions from baseline to follow-up scans with acceptable reliability. Elsevier 2020-09-24 /pmc/articles/PMC7554211/ /pubmed/33038667 http://dx.doi.org/10.1016/j.nicl.2020.102445 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Krüger, Julia
Opfer, Roland
Gessert, Nils
Ostwaldt, Ann-Christin
Manogaran, Praveena
Kitzler, Hagen H.
Schlaefer, Alexander
Schippling, Sven
Fully automated longitudinal segmentation of new or enlarged multiple sclerosis lesions using 3D convolutional neural networks
title Fully automated longitudinal segmentation of new or enlarged multiple sclerosis lesions using 3D convolutional neural networks
title_full Fully automated longitudinal segmentation of new or enlarged multiple sclerosis lesions using 3D convolutional neural networks
title_fullStr Fully automated longitudinal segmentation of new or enlarged multiple sclerosis lesions using 3D convolutional neural networks
title_full_unstemmed Fully automated longitudinal segmentation of new or enlarged multiple sclerosis lesions using 3D convolutional neural networks
title_short Fully automated longitudinal segmentation of new or enlarged multiple sclerosis lesions using 3D convolutional neural networks
title_sort fully automated longitudinal segmentation of new or enlarged multiple sclerosis lesions using 3d convolutional neural networks
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7554211/
https://www.ncbi.nlm.nih.gov/pubmed/33038667
http://dx.doi.org/10.1016/j.nicl.2020.102445
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