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Leveraging hand-crafted radiomics on multicenter FLAIR MRI for predicting disability worsening in people with multiple sclerosis

 
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cris.virtual.orcid0000-0003-4225-2487
cris.virtual.orcid0000-0001-9778-1031
cris.virtual.orcid0000-0001-9976-1886
cris.virtualsource.department33ee4c5e-70fd-4640-9a4b-6dff3f3210d0
cris.virtualsource.departmentd60193dd-aa95-4136-94c9-bbc7723ef38a
cris.virtualsource.departmentcc0b1187-8a70-4d2c-a8fa-da0696edd7c5
cris.virtualsource.orcid33ee4c5e-70fd-4640-9a4b-6dff3f3210d0
cris.virtualsource.orcidd60193dd-aa95-4136-94c9-bbc7723ef38a
cris.virtualsource.orcidcc0b1187-8a70-4d2c-a8fa-da0696edd7c5
dc.contributor.authorKhan, Hamza
dc.contributor.authorWoodruff, Henry C.
dc.contributor.authorGiraldo Franco, Diana
dc.contributor.authorWerthen Brabants, Lorin
dc.contributor.authorMali, Shruti Atul
dc.contributor.authorAmirrajab, Sina
dc.contributor.authorDe Brouwer, Edward
dc.contributor.authorPopescu, Veronica
dc.contributor.authorVan Wijmeersch, Bart
dc.contributor.authorGerlach, Oliver
dc.contributor.authorSijbers, Jan
dc.contributor.authorPeeters, Liesbet M.
dc.contributor.authorLambin, Philippe
dc.date.accessioned2026-02-02T14:12:33Z
dc.date.available2026-02-02T14:12:33Z
dc.date.createdwos2025-11-17
dc.date.issued2025
dc.description.abstractBackground: Multiple sclerosis (MS) is an autoimmune disease of the central nervous system, leading to varying degrees of functional impairment. Conventional tools, such as the Expanded Disability Status Scale (EDSS), lack sensitivity to subtle disease worsening. Radiomics provides a quantitative imaging approach to address this limitation. This study applied machine learning (ML) and radiomics features from T2-weighted Fluid-Attenuated Inversion Recovery (FLAIR) magnetic resonance imaging (MRI) to predict disability worsening in MS. Methods: A retrospective analysis was performed on real-world data from 247 PwMS across two centers. Disability worsening was defined as a change in EDSS over two years. FLAIR MRIs underwent preprocessing and super-resolution reconstruction to enhance low-resolution images. White matter lesions (WML) were segmented using the Lesion Segmentation Toolbox (LST), and tissue segmentation was performed using sequence Adaptive Multimodal Segmentation. Radiomics features from WML and normal-appearing white matter (NAWM) were extracted using Pyradiomics, harmonized with Longitudinal ComBat, followed by recursive feature elimination for feature selection. Elastic Net, Balanced Random Forest (BRFC), and Light Gradient-Boosting Machine (LGBM) models were trained and evaluated. Results: The LGBM model with harmonized radiomics and clinical features outperformed the clinical-only model, achieving a test area under the precision-recall curve (PR AUC) of 0.20 and a receiver operating characteristic area under the curve (ROC AUC) of 0.64. Key predictive features, among others, included Gray-Level Co-Occurrence Matrix (GLCM) maximum probability (WML) and Gray-Level Dependence Matrix (GLDM) dependence non-uniformity (NAWM). However, short-term longitudinal changes showed limited predictive power (PR AUC = 0.11, ROC AUC = 0.69). Conclusion: These findings highlight the potential of ML-driven radiomics in predicting disability worsening, warranting validation in larger, balanced datasets and exploration of advanced deep learning approaches. Highlights • Machine learning improves the prediction of disability worsening in multiple sclerosis. • Radiomics can capture subtle, diffuse changes in MS worsening from FLAIR MRI. • Super-resolution reconstruction enhances radiomics analysis of low-resolution MRIs.
dc.description.wosFundingTextThe author(s) declare that financial support was received for the research and/or publication of this article. This research received funding from the Flemish Government under the "Onderzoeksprogramma Artificiele Intelligentie (AI) Vlaanderen" program, Stichting Multiple Sclerosis Research (19-1040 MS) and the Bijzonder OnderzoeksFonds (BOF19DOCMA10). Authors acknowledge financial support from the European Union's Horizon research and innovation programme under grant agreements: ImmunoSABR n degrees 733008, CHAIMELEON n degrees 952172, EuCanImage n degrees 952103, IMI-OPTIMA n degrees 101034347, RADIOVAL (HORIZON-HLTH-2021-DISEASE-04-04) n degrees 101057699, EUCAIM (DIGITAL-2022-CLOUD-AI-02) n degrees 101100633, GLIOMATCH n degrees 101136670, AIDAVA (HORIZON-HLTH-2021-TOOL-06) n degrees 101057062, and REALM (HORIZON-HLTH-2022-TOOL-11) n degrees 101095435.
dc.identifier.doi10.3389/fnins.2025.1610401
dc.identifier.issn1662-453X
dc.identifier.pmidMEDLINE:41235171
dc.identifier.urihttps://imec-publications.be/handle/20.500.12860/58765
dc.language.isoeng
dc.provenance.editstepusergreet.vanhoof@imec.be
dc.publisherFRONTIERS MEDIA SA
dc.source.beginpage1610401
dc.source.journalFRONTIERS IN NEUROSCIENCE
dc.source.numberofpages16
dc.source.volume19
dc.subject.keywordsTEXTURE ANALYSIS
dc.subject.keywordsIMAGES
dc.subject.keywordsBRAIN
dc.subject.keywordsLESIONS
dc.subject.keywordsRECOMMENDATIONS
dc.subject.keywordsCLASSIFICATION
dc.subject.keywordsDIAGNOSIS
dc.title

Leveraging hand-crafted radiomics on multicenter FLAIR MRI for predicting disability worsening in people with multiple sclerosis

dc.typeJournal article
dspace.entity.typePublication
imec.internal.crawledAt2025-11-20
imec.internal.sourcecrawler
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