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Scanner agnostic large-scale evaluation of MS lesion delineation tool for clinical MRI
INTRODUCTION: Patients with MS are MRI scanned continuously throughout their disease course resulting in a large manual workload for radiologists which includes lesion detection and size estimation. Though many models for automatic lesion segmentation have been published, few are used broadly in cli...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235534/ https://www.ncbi.nlm.nih.gov/pubmed/37274207 http://dx.doi.org/10.3389/fnins.2023.1177540 |
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author | Hindsholm, Amalie Monberg Andersen, Flemming Littrup Cramer, Stig Præstekjær Simonsen, Helle Juhl Askløf, Mathias Gæde Magyari, Melinda Madsen, Poul Nørgaard Hansen, Adam Espe Sellebjerg, Finn Larsson, Henrik Bo Wiberg Langkilde, Annika Reynberg Frederiksen, Jette Lautrup Højgaard, Liselotte Ladefoged, Claes Nøhr Lindberg, Ulrich |
author_facet | Hindsholm, Amalie Monberg Andersen, Flemming Littrup Cramer, Stig Præstekjær Simonsen, Helle Juhl Askløf, Mathias Gæde Magyari, Melinda Madsen, Poul Nørgaard Hansen, Adam Espe Sellebjerg, Finn Larsson, Henrik Bo Wiberg Langkilde, Annika Reynberg Frederiksen, Jette Lautrup Højgaard, Liselotte Ladefoged, Claes Nøhr Lindberg, Ulrich |
author_sort | Hindsholm, Amalie Monberg |
collection | PubMed |
description | INTRODUCTION: Patients with MS are MRI scanned continuously throughout their disease course resulting in a large manual workload for radiologists which includes lesion detection and size estimation. Though many models for automatic lesion segmentation have been published, few are used broadly in clinic today, as there is a lack of testing on clinical datasets. By collecting a large, heterogeneous training dataset directly from our MS clinic we aim to present a model which is robust to different scanner protocols and artefacts and which only uses MRI modalities present in routine clinical examinations. METHODS: We retrospectively included 746 patients from routine examinations at our MS clinic. The inclusion criteria included acquisition at one of seven different scanners and an MRI protocol including 2D or 3D T2-w FLAIR, T2-w and T1-w images. Reference lesion masks on the training (n = 571) and validation (n = 70) datasets were generated using a preliminary segmentation model and subsequent manual correction. The test dataset (n = 100) was manually delineated. Our segmentation model https://github.com/CAAI/AIMS/ was based on the popular nnU-Net, which has won several biomedical segmentation challenges. We tested our model against the published segmentation models HD-MS-Lesions, which is also based on nnU-Net, trained with a more homogenous patient cohort. We furthermore tested model robustness to data from unseen scanners by performing a leave-one-scanner-out experiment. RESULTS: We found that our model was able to segment MS white matter lesions with a performance comparable to literature: DSC = 0.68, precision = 0.90, recall = 0.70, f1 = 0.78. Furthermore, the model outperformed HD-MS-Lesions in all metrics except precision = 0.96. In the leave-one-scanner-out experiment there was no significant change in performance (p < 0.05) between any of the models which were only trained on part of the dataset and the full segmentation model. CONCLUSION: In conclusion we have seen, that by including a large, heterogeneous dataset emulating clinical reality, we have trained a segmentation model which maintains a high segmentation performance while being robust to data from unseen scanners. This broadens the applicability of the model in clinic and paves the way for clinical implementation. |
format | Online Article Text |
id | pubmed-10235534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102355342023-06-03 Scanner agnostic large-scale evaluation of MS lesion delineation tool for clinical MRI Hindsholm, Amalie Monberg Andersen, Flemming Littrup Cramer, Stig Præstekjær Simonsen, Helle Juhl Askløf, Mathias Gæde Magyari, Melinda Madsen, Poul Nørgaard Hansen, Adam Espe Sellebjerg, Finn Larsson, Henrik Bo Wiberg Langkilde, Annika Reynberg Frederiksen, Jette Lautrup Højgaard, Liselotte Ladefoged, Claes Nøhr Lindberg, Ulrich Front Neurosci Neuroscience INTRODUCTION: Patients with MS are MRI scanned continuously throughout their disease course resulting in a large manual workload for radiologists which includes lesion detection and size estimation. Though many models for automatic lesion segmentation have been published, few are used broadly in clinic today, as there is a lack of testing on clinical datasets. By collecting a large, heterogeneous training dataset directly from our MS clinic we aim to present a model which is robust to different scanner protocols and artefacts and which only uses MRI modalities present in routine clinical examinations. METHODS: We retrospectively included 746 patients from routine examinations at our MS clinic. The inclusion criteria included acquisition at one of seven different scanners and an MRI protocol including 2D or 3D T2-w FLAIR, T2-w and T1-w images. Reference lesion masks on the training (n = 571) and validation (n = 70) datasets were generated using a preliminary segmentation model and subsequent manual correction. The test dataset (n = 100) was manually delineated. Our segmentation model https://github.com/CAAI/AIMS/ was based on the popular nnU-Net, which has won several biomedical segmentation challenges. We tested our model against the published segmentation models HD-MS-Lesions, which is also based on nnU-Net, trained with a more homogenous patient cohort. We furthermore tested model robustness to data from unseen scanners by performing a leave-one-scanner-out experiment. RESULTS: We found that our model was able to segment MS white matter lesions with a performance comparable to literature: DSC = 0.68, precision = 0.90, recall = 0.70, f1 = 0.78. Furthermore, the model outperformed HD-MS-Lesions in all metrics except precision = 0.96. In the leave-one-scanner-out experiment there was no significant change in performance (p < 0.05) between any of the models which were only trained on part of the dataset and the full segmentation model. CONCLUSION: In conclusion we have seen, that by including a large, heterogeneous dataset emulating clinical reality, we have trained a segmentation model which maintains a high segmentation performance while being robust to data from unseen scanners. This broadens the applicability of the model in clinic and paves the way for clinical implementation. Frontiers Media S.A. 2023-05-19 /pmc/articles/PMC10235534/ /pubmed/37274207 http://dx.doi.org/10.3389/fnins.2023.1177540 Text en Copyright © 2023 Hindsholm, Andersen, Cramer, Simonsen, Askløf, Magyari, Madsen, Hansen, Sellebjerg, Larsson, Langkilde, Frederiksen, Højgaard, Ladefoged and Lindberg. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Hindsholm, Amalie Monberg Andersen, Flemming Littrup Cramer, Stig Præstekjær Simonsen, Helle Juhl Askløf, Mathias Gæde Magyari, Melinda Madsen, Poul Nørgaard Hansen, Adam Espe Sellebjerg, Finn Larsson, Henrik Bo Wiberg Langkilde, Annika Reynberg Frederiksen, Jette Lautrup Højgaard, Liselotte Ladefoged, Claes Nøhr Lindberg, Ulrich Scanner agnostic large-scale evaluation of MS lesion delineation tool for clinical MRI |
title | Scanner agnostic large-scale evaluation of MS lesion delineation tool for clinical MRI |
title_full | Scanner agnostic large-scale evaluation of MS lesion delineation tool for clinical MRI |
title_fullStr | Scanner agnostic large-scale evaluation of MS lesion delineation tool for clinical MRI |
title_full_unstemmed | Scanner agnostic large-scale evaluation of MS lesion delineation tool for clinical MRI |
title_short | Scanner agnostic large-scale evaluation of MS lesion delineation tool for clinical MRI |
title_sort | scanner agnostic large-scale evaluation of ms lesion delineation tool for clinical mri |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235534/ https://www.ncbi.nlm.nih.gov/pubmed/37274207 http://dx.doi.org/10.3389/fnins.2023.1177540 |
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