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Machine learning in lupus nephritis: bridging prediction models and clinical decision-making towards personalized nephrology

dc.contributor.authorGarcia-Bañol, Diego Fernando
dc.contributor.authorArias-Choles, Adrianny Mahelis
dc.contributor.authorAldana-Peréz, Silvia
dc.contributor.authorAroca-Martínez, Gustavo J.
dc.contributor.authorMusso, Carlos Guido
dc.contributor.authorNavarro-Quiroz, Roberto [UNESP]
dc.contributor.authorDominguez-Vargas, Alex
dc.contributor.authorGonzalez-Torres, Henry J.
dc.date.accessioned2026-04-13T14:07:41Z
dc.date.issued2025-10-29
dc.description.abstractBackground: Lupus nephritis (LN) is one of the most severe manifestations of systemic lupus erythematosus (SLE), affecting up to 65% of patients and contributing significantly to morbidity and mortality. The heterogeneous clinical course of LN-characterized by alternating flares and remissions-stems from complex immunological, genetic, endocrine, and environmental factors. Current management strategies rely on immunosuppressants and corticosteroids, yet predicting disease progression, treatment response, and relapse risk remains challenging. Objective: This review synthesizes current evidence on the use of machine learning (ML) models for predicting, diagnosing, and monitoring LN, emphasizing their translational potential to improve clinical decision-making and enable personalized nephrology. Methods: A narrative synthesis was conducted of studies published between 2015 and April 2024, identified through PubMed using the terms ("lupus nephritis" OR "LN") AND ("machine learning" OR "artificial intelligence" OR "deep learning"). Eligible studies included those applying ML models to LN for diagnosis, histological classification, flare prediction, treatment response, or prognosis. Results: We identified diverse ML approaches-including logistic regression, decision trees, random forests, support vector machines, neural networks, gradient boosting, and clustering-applied to multimodal data sources (clinical, laboratory, imaging, histopathology, and omics). These models demonstrated high performance in tasks such as non-invasive histology classification (AUC up to 0.98), flare prediction, and individualized risk stratification. Integration with big data frameworks enhanced the identification of molecular drivers, improved prognostic accuracy, and facilitated remote patient monitoring. However, model development in LN remains limited by small datasets, lack of external validation, and heterogeneous outcome definitions. Conclusion: ML models have the potential to transform LN management by enabling earlier flare detection, personalized treatment strategies, and non-invasive disease monitoring. To achieve clinical integration, future research must prioritize robust validation, interoperability with electronic health records, and transparent model interpretability. Bridging the gap between computational performance and real-world application could substantially improve outcomes and quality of life for LN patients.
dc.description.affiliationFacultad de Ciencias de la Salud, Centro de Investigaciones en Ciencias de la Vida, Universidad Simón Bolívar, Barranquilla, Colombia
dc.description.affiliationClínica de la Costa, Departamento de Medicina Interna, Barranquilla, Colombia
dc.description.affiliationDepartamento de Fisiología Renal, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina
dc.description.affiliationUniversidade Estadual Paulista, Instituto de Química, São Paulo, Brazil
dc.description.affiliationData Analysis and Mining Department, Data & Project Consulting Service SAS, Barranquilla, Colombia
dc.description.affiliationUnespUniversidade Estadual Paulista, Instituto de Química, São Paulo, Brazil
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1194404285
dc.identifier.dimensionspub.1194404285
dc.identifier.doi10.3389/fmed.2025.1686057
dc.identifier.issn2296-858X
dc.identifier.orcid0000-0001-8666-1130
dc.identifier.orcid0000-0002-3604-3702
dc.identifier.orcid0000-0002-3984-8653
dc.identifier.orcid0000-0001-7434-4568
dc.identifier.pmcidPMC12605162
dc.identifier.pmid41234906
dc.identifier.urihttps://hdl.handle.net/11449/321625
dc.publisherFrontiers
dc.relation.ispartofFrontiers in Medicine; v. 12; p. 1686057
dc.rights.accessRightsAcesso abertopt
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dc.rights.sourceRightsgold
dc.sourceDimensions
dc.titleMachine learning in lupus nephritis: bridging prediction models and clinical decision-making towards personalized nephrology
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt

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