Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/46540
Title: Personalized federated learning for predicting disability progression in multiple sclerosis using real-world routine clinical data
Authors: PIRMANI, Ashkan 
DE BROUWER, Edward 
Arany, Adam
Oldenhof, Martijn
Passemiers, Antoine
FAES, Axel 
Kalincik, Tomas
Ozakbas, Serkan
Gouider, Riadh
Willekens, Barbara
Horakova, Dana
Havrdova, Eva Kubala
Patti, Francesco
Prat, Alexandre
Lugaresi, Alessandra
Tomassini, Valentina
Grammond, Pierre
Cartechini, Elisabetta
Roos, Izanne
Boz, Cavit
Alroughani, Raed
Amato, Maria Pia
Buzzard, Katherine
Lechner-Scott, Jeannette
Guimaraes, Joana
Solaro, Claudio
Gerlach, Oliver
Soysal, Aysun
Kuhle, Jens
Sanchez-Menoyo, Jose Luis
Spitaleri, Daniele
Csepany, Tunde
VAN WIJMEERSCH, Bart 
Ampapa, Radek
Prevost, Julie
Khoury, Samia J.
Van Pesch, Vincent
John, Nevin
Maimone, Davide
Weinstock-Guttman, Bianca
Laureys, Guy
Mccombe, Pamela
Blanco, Yolanda
Altintas , Ayse
Al-Asmi, Abdullah
Garber, Justin
van der Walt, Anneke
Butzkueven, Helmut
de Gans, Koen
Rozsa, Csilla
Taylor, Bruce
Al-Harbi, Talal
Sas, Attila
Rajda, Cecilia
Gray, Orla
Decoo, Danny
Carroll, William M.
Kermode, Allan G.
Fabis-Pedrini, Marzena
Mason, Deborah
Perez-Sempere, Angel
Simu, Mihaela
Shuey, Neil
Singhal, Bhim
Cauchi, Marija
Hardy, Todd A.
Ramanathan, Sudarshini
Lalive, Patrice
Sirbu, Carmen-Adella
Hughes, Stella
Castillo Trivino, Tamara
PEETERS, Liesbet 
Moreau, Yves
Issue Date: 2025
Publisher: NATURE PORTFOLIO
Source: npj digital medicine, 8 (1) (Art N° 478)
Abstract: Early prediction of disability progression in multiple sclerosis (MS) remains challenging despite its critical importance for therapeutic decision-making. We present the first systematic evaluation of personalized federated learning (PFL) for 2-year MS disability progression prediction, leveraging multi-center real-world data from over 26,000 patients. While conventional federated learning (FL) enables privacy-aware collaborative modeling, it remains vulnerable to institutional data heterogeneity. PFL overcomes this challenge by adapting shared models to local data distributions without compromising privacy. We evaluated two personalization strategies: a novel AdaptiveDualBranchNet architecture with selective parameter sharing, and personalized fine-tuning of global models, benchmarked against centralized and client-specific approaches. Baseline FL underperformed relative to personalized methods, whereas personalization significantly improved performance, with personalized FedProx and FedAVG achieving ROC-AUC scores of 0.8398 +/- 0.0019 and 0.8384 +/- 0.0014, respectively. These findings establish personalization as critical for scalable, privacy-aware clinical prediction models and highlight its potential to inform earlier intervention strategies in MS and beyond.
Notes: Moreau, Y (corresponding author), ESAT KU Leuven, STADIUS, Leuven, Belgium.
Yves.Moreau@esat.kuleuven.be
Document URI: http://hdl.handle.net/1942/46540
ISSN: 2398-6352
e-ISSN: 2398-6352
DOI: 10.1038/s41746-025-01788-8
ISI #: 001536298500003
Rights: The Author(s) 2025. Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/bync-nd/4.0/.
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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