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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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