Partial volume-aware assessment of multiple sclerosis lesions
White-matter lesion count and volume estimation are key to the diagnosis and monitoring of multiple sclerosis (MS). Automated MS lesion segmentation methods that have been proposed in the past 20 years reach their limits when applied to patients in early disease stages characterized by low lesion lo...
| Published in: | NeuroImage: Clinical |
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| Main Authors: | , , , , , , , , |
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2018-01-01
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| Online Access: | http://www.sciencedirect.com/science/article/pii/S2213158218300111 |
| _version_ | 1852748298660610048 |
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| author | Mário João Fartaria Alexandra Todea Tobias Kober Kieran O'brien Gunnar Krueger Reto Meuli Cristina Granziera Alexis Roche Meritxell Bach Cuadra |
| author_facet | Mário João Fartaria Alexandra Todea Tobias Kober Kieran O'brien Gunnar Krueger Reto Meuli Cristina Granziera Alexis Roche Meritxell Bach Cuadra |
| author_sort | Mário João Fartaria |
| collection | DOAJ |
| container_title | NeuroImage: Clinical |
| description | White-matter lesion count and volume estimation are key to the diagnosis and monitoring of multiple sclerosis (MS). Automated MS lesion segmentation methods that have been proposed in the past 20 years reach their limits when applied to patients in early disease stages characterized by low lesion load and small lesions. We propose an algorithm to automatically assess MS lesion load (number and volume) while taking into account the mixing of healthy and lesional tissue in the image voxels due to partial volume effects. The proposed method works on 3D MPRAGE and 3D FLAIR images as obtained from current routine MS clinical protocols. The method was evaluated and compared with manual segmentation on a cohort of 39 early-stage MS patients with low disability, and showed higher Dice similarity coefficients (median DSC = 0.55) and higher detection rate (median DR = 61%) than two widely used methods (median DSC = 0.50, median DR < 45%) for automated MS lesion segmentation. We argue that this is due to the higher performance in segmentation of small lesions, which are inherently prone to partial volume effects. Keywords: Partial volume, Multiple sclerosis, MRI, Lesion segmentation |
| format | Article |
| id | doaj-art-85c816e778bb45f8b325fbb514b9f85a |
| institution | Directory of Open Access Journals |
| issn | 2213-1582 |
| language | English |
| publishDate | 2018-01-01 |
| publisher | Elsevier |
| record_format | Article |
| spelling | doaj-art-85c816e778bb45f8b325fbb514b9f85a2025-08-19T21:01:24ZengElsevierNeuroImage: Clinical2213-15822018-01-011824525310.1016/j.nicl.2018.01.011Partial volume-aware assessment of multiple sclerosis lesionsMário João Fartaria0Alexandra Todea1Tobias Kober2Kieran O'brien3Gunnar Krueger4Reto Meuli5Cristina Granziera6Alexis Roche7Meritxell Bach Cuadra8Advanced Clinical Imaging Technology (HC CMEA SUI DI PI), Siemens Healthcare AG, Lausanne, Switzerland; Department of Radiology, Lausanne University Hospital (CHUV), and University of Lausanne (UNIL), Lausanne, Switzerland; Signal Processing Laboratory (LTS 5), Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland; Corresponding author at: Advanced Clinical Imaging Technology (HC CMEA SUI DI PI), Siemens Healthcare AG, Lausanne, Switzerland.Department of Radiology, Pourtalès Hospital, Neuchâtel, SwitzerlandAdvanced Clinical Imaging Technology (HC CMEA SUI DI PI), Siemens Healthcare AG, Lausanne, Switzerland; Department of Radiology, Lausanne University Hospital (CHUV), and University of Lausanne (UNIL), Lausanne, Switzerland; Signal Processing Laboratory (LTS 5), Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, SwitzerlandCentre for Advanced Imaging, University of Queensland, Queensland, Australia; Siemens Healthcare Pty. Ltd., Brisbane, Queensland, AustraliaSiemens Healthcare Ltd, Zürich, SwitzerlandDepartment of Radiology, Lausanne University Hospital (CHUV), and University of Lausanne (UNIL), Lausanne, SwitzerlandNeurologic Clinic and Policlinic, Departments of Medicine, Clinical Research and Biomedical Engineering, University Hospital Basel and University of Basel, Basel, Switzerland; Translational Imaging in Neurology (ThINK) Basel, Department of Medicine and Biomedical Engineering, University Hospital Basel and University of Basel, Basel, SwitzerlandDepartment of Radiology, Lausanne University Hospital (CHUV), and University of Lausanne (UNIL), Lausanne, Switzerland; Advanced Clinical Imaging Technology (HC CMEA SUI DI PI), Siemens Healthcare AG, Lausanne, Switzerland; Signal Processing Laboratory (LTS 5), Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, SwitzerlandDepartment of Radiology, Lausanne University Hospital (CHUV), and University of Lausanne (UNIL), Lausanne, Switzerland; Medical Image Analysis Laboratory (MIAL), Centre d'Imagerie BioMédicale (CIBM), Lausanne, Switzerland; Signal Processing Laboratory (LTS 5), Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, SwitzerlandWhite-matter lesion count and volume estimation are key to the diagnosis and monitoring of multiple sclerosis (MS). Automated MS lesion segmentation methods that have been proposed in the past 20 years reach their limits when applied to patients in early disease stages characterized by low lesion load and small lesions. We propose an algorithm to automatically assess MS lesion load (number and volume) while taking into account the mixing of healthy and lesional tissue in the image voxels due to partial volume effects. The proposed method works on 3D MPRAGE and 3D FLAIR images as obtained from current routine MS clinical protocols. The method was evaluated and compared with manual segmentation on a cohort of 39 early-stage MS patients with low disability, and showed higher Dice similarity coefficients (median DSC = 0.55) and higher detection rate (median DR = 61%) than two widely used methods (median DSC = 0.50, median DR < 45%) for automated MS lesion segmentation. We argue that this is due to the higher performance in segmentation of small lesions, which are inherently prone to partial volume effects. Keywords: Partial volume, Multiple sclerosis, MRI, Lesion segmentationhttp://www.sciencedirect.com/science/article/pii/S2213158218300111 |
| spellingShingle | Mário João Fartaria Alexandra Todea Tobias Kober Kieran O'brien Gunnar Krueger Reto Meuli Cristina Granziera Alexis Roche Meritxell Bach Cuadra Partial volume-aware assessment of multiple sclerosis lesions |
| title | Partial volume-aware assessment of multiple sclerosis lesions |
| title_full | Partial volume-aware assessment of multiple sclerosis lesions |
| title_fullStr | Partial volume-aware assessment of multiple sclerosis lesions |
| title_full_unstemmed | Partial volume-aware assessment of multiple sclerosis lesions |
| title_short | Partial volume-aware assessment of multiple sclerosis lesions |
| title_sort | partial volume aware assessment of multiple sclerosis lesions |
| url | http://www.sciencedirect.com/science/article/pii/S2213158218300111 |
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