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Contrast-Enhancing Lesion Segmentation in Multiple Sclerosis: A Deep Learning Approach Validated in a Multicentric Cohort

Authors :
Martina Greselin
Po-Jui Lu
Lester Melie-Garcia
Mario Ocampo-Pineda
Riccardo Galbusera
Alessandro Cagol
Matthias Weigel
Nina de Oliveira Siebenborn
Esther Ruberte
Pascal Benkert
Stefanie Müller
Sebastian Finkener
Jochen Vehoff
Giulio Disanto
Oliver Findling
Andrew Chan
Anke Salmen
Caroline Pot
Claire Bridel
Chiara Zecca
Tobias Derfuss
Johanna M. Lieb
Michael Diepers
Franca Wagner
Maria I. Vargas
Renaud Du Pasquier
Patrice H. Lalive
Emanuele Pravatà
Johannes Weber
Claudio Gobbi
David Leppert
Olaf Chan-Hi Kim
Philippe C. Cattin
Robert Hoepner
Patrick Roth
Ludwig Kappos
Jens Kuhle
Cristina Granziera
Source :
Bioengineering, Vol 11, Iss 8, p 858 (2024)
Publication Year :
2024
Publisher :
MDPI AG, 2024.

Abstract

The detection of contrast-enhancing lesions (CELs) is fundamental for the diagnosis and monitoring of patients with multiple sclerosis (MS). This task is time-consuming and suffers from high intra- and inter-rater variability in clinical practice. However, only a few studies proposed automatic approaches for CEL detection. This study aimed to develop a deep learning model that automatically detects and segments CELs in clinical Magnetic Resonance Imaging (MRI) scans. A 3D UNet-based network was trained with clinical MRI from the Swiss Multiple Sclerosis Cohort. The dataset comprised 372 scans from 280 MS patients: 162 showed at least one CEL, while 118 showed no CELs. The input dataset consisted of T1-weighted before and after gadolinium injection, and FLuid Attenuated Inversion Recovery images. The sampling strategy was based on a white matter lesion mask to confirm the existence of real contrast-enhancing lesions. To overcome the dataset imbalance, a weighted loss function was implemented. The Dice Score Coefficient and True Positive and False Positive Rates were 0.76, 0.93, and 0.02, respectively. Based on these results, the model developed in this study might well be considered for clinical decision support.

Details

Language :
English
ISSN :
23065354
Volume :
11
Issue :
8
Database :
Directory of Open Access Journals
Journal :
Bioengineering
Publication Type :
Academic Journal
Accession number :
edsdoj.753b7b7b06c042a89d9dbeabe7219d4d
Document Type :
article
Full Text :
https://doi.org/10.3390/bioengineering11080858