New multiple sclerosis lesion segmentation and detection using pre-activation U-Net

Automated segmentation of new multiple sclerosis (MS) lesions in 3D MRI data is an essential prerequisite for monitoring and quantifying MS progression. Manual delineation of such lesions is time-consuming and expensive, especially because raters need to deal with 3D images and several modalities. I...

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Veröffentlicht in:Frontiers in neuroscience Jg. 16; S. 975862
Hauptverfasser: Ashtari, Pooya, Barile, Berardino, Van Huffel, Sabine, Sappey-Marinier, Dominique
Format: Journal Article
Sprache:Englisch
Veröffentlicht: Lausanne Frontiers Research Foundation 26.10.2022
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Frontiers Media S.A
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ISSN:1662-453X, 1662-4548, 1662-453X
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Zusammenfassung:Automated segmentation of new multiple sclerosis (MS) lesions in 3D MRI data is an essential prerequisite for monitoring and quantifying MS progression. Manual delineation of such lesions is time-consuming and expensive, especially because raters need to deal with 3D images and several modalities. In this paper, we propose Pre-U-Net, a 3D encoder-decoder architecture with pre-activation residual blocks, for the segmentation and detection of new MS lesions. Due to the limited training set and the class imbalance problem, we apply intensive data augmentation and use deep supervision to train our models effectively. Following the same U-shaped architecture but different blocks, Pre-U-Net outperforms U-Net and Res-U-Net on the MSSEG-2 dataset, achieving a Dice score of 40.3% on new lesion segmentation and an F 1 score of 48.1% on new lesion detection. The codes and trained models are publicly available at https://github.com/pashtari/xunet .
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This article was submitted to Brain Imaging Methods, a section of the journal Frontiers in Neuroscience
Edited by: Michel Dojat, Institut National de la Santé et de la Recherche Médicale (INSERM), France
Reviewed by: Shen Zhao, Sun Yat-sen University, China; Cédric Meurée, Inria Rennes—Bretagne Atlantique Research Centre, France
ISSN:1662-453X
1662-4548
1662-453X
DOI:10.3389/fnins.2022.975862