Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/45766
Title: Machine-learning-based prediction of disability progression in multiple sclerosis: An observational, international, multi-center study
Authors: DE BROUWER, Edward 
BECKER, Thijs 
Werthen-Brabants, Lorin
Dewulf, Pieter
Iliadis, Dimitrios
DEKEYSER, Catherine 
Laureys, Guy
Dhaene, Tom
VAN WIJMEERSCH, Bart 
Deschrijver, Dirk
POPESCU, Veronica 
Waegeman, Willem
De Baets , Bernard
Stock, Michiel
Horakova, Dana
Patti, Francesco
Izquierdo, Guillermo
Eichau, Sara
Girard, Marc
Prat, Alexandre
Lugaresi, Alessandra
Grammond, Pierre
Kalincik, Tomas
Alroughani, Raed
Grand'Maison, Francois
Skibina, Olga
Terzi, Murat
Lechner-Scott, Jeannette
Gerlach, Oliver
Khoury, Samia J.
Cartechini, Elisabetta
Van Pesch, Vincent
Sa, Maria Jose
Weinstock-Guttman, Bianca
Blanco, Yolanda
Ampapa, Radek
Spitaleri, Daniele
Solaro, Claudio
Maimone, Davide
Soysal, Aysun
Iuliano, Gerardo
Gouider, Riadh
Castillo-Trivino, Tamara
Luis Sanchez-Menoyo, Jose
van der Walt, Anneke
Oh, Jiwon
Aguera-Morales, Eduardo
Altintas , Ayse
Al-Asmi, Abdullah
de Gans, Koen
Fragoso, Yara
Csepany, Tunde
Hodgkinson, Suzanne
Deri, Norma
Al-Harbi, Talal
Taylor, Bruce
Gray, Orla
Lalive, Patrice
Rozsa, Csilla
McGuigan, Chris
Kermode, Allan
Perez Sempere, Angel
Mihaela, Simu
Simo, Magdolna
Hardy, Todd
Decoo, Danny
Hughes, Stella
Grigoriadis, Nikolaos
Sas, Attila
Vella, Norbert
Moreau, Yves
PEETERS, Liesbet 
Editors: McGinnis, Ryan S
Issue Date: 2024
Publisher: PUBLIC LIBRARY SCIENCE
Source: Plos Digital Health, 3 (7) (Art N° e0000533)
Abstract: Background Disability progression is a key milestone in the disease evolution of people with multiple sclerosis (PwMS). Prediction models of the probability of disability progression have not yet reached the level of trust needed to be adopted in the clinic. A common benchmark to assess model development in multiple sclerosis is also currently lacking. Methods Data of adult PwMS with a follow-up of at least three years from 146 MS centers, spread over 40 countries and collected by the MSBase consortium was used. With basic inclusion criteria for quality requirements, it represents a total of 15, 240 PwMS. External validation was performed and repeated five times to assess the significance of the results. Transparent Reporting for Individual Prognosis Or Diagnosis (TRIPOD) guidelines were followed. Confirmed disability progression after two years was predicted, with a confirmation window of six months. Only routinely collected variables were used such as the expanded disability status scale, treatment, relapse information, and MS course. To learn the probability of disability progression, state-of-the-art machine learning models were investigated. The discrimination performance of the models is evaluated with the area under the receiver operator curve (ROC-AUC) and under the precision recall curve (AUC-PR), and their calibration via the Brier score and the expected calibration error. All our preprocessing and model code are available at https://gitlab.com/edebrouwer/ms_benchmark, making this task an ideal benchmark for predicting disability progression in MS. Findings Machine learning models achieved a ROC-AUC of 0.71 +/- 0.01, an AUC-PR of 0.26 +/- 0.02, a Brier score of 0.1 +/- 0.01 and an expected calibration error of 0.07 +/- 0.04. The history of disability progression was identified as being more predictive for future disability progression than the treatment or relapses history. Conclusions Good discrimination and calibration performance on an external validation set is achieved, using only routinely collected variables. This suggests machine-learning models can reliably inform clinicians about the future occurrence of progression and are mature for a clinical impact study.
Notes: Peeters, L (corresponding author), Hasselt Univ, Data Sci Inst, Hasselt, Belgium.; Peeters, L (corresponding author), Univ MS Ctr Hasselt Pelt, Hasselt, Belgium.
liesbet.peeters@uhasselt.be
Document URI: http://hdl.handle.net/1942/45766
e-ISSN: 2767-3170
DOI: 10.1371/journal.pdig.0000533
ISI #: 001439561000001
Datasets of the publication: 10.1371/journal.pdig.0000533.t001
Rights: 2024 De Brouwer et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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