<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-17T02:45:03Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:11351/8651" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:11351/8651</identifier><datestamp>2025-10-24T10:29:46Z</datestamp><setSpec>com_2072_378070</setSpec><setSpec>com_2072_378040</setSpec><setSpec>col_2072_378092</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Using Interpretable Machine Learning to Identify Baseline Predictive Factors of Remission and Drug Durability in Crohn’s Disease Patients on Ustekinumab</dc:title>
   <dc:creator>Fernández Salgado, Estela</dc:creator>
   <dc:creator>Robles Alonso, Virginia</dc:creator>
   <dc:creator>Chaparro, María</dc:creator>
   <dc:creator>Baston Rey, Iria</dc:creator>
   <dc:creator>González García, Javier</dc:creator>
   <dc:creator>Ramos, Laura</dc:creator>
   <dc:creator>Diz-Lois Palomares, Mª Teresa</dc:creator>
   <dc:subject>Crohn, Malaltia de - Tractament</dc:subject>
   <dc:subject>Antiinflamatoris - Ús terapèutic</dc:subject>
   <dc:subject>Aprenentatge automàtic</dc:subject>
   <dc:subject>INFORMATION SCIENCE::Information Science::Computing Methodologies::Algorithms::Artificial Intelligence::Machine Learning</dc:subject>
   <dc:subject>DISEASES::Digestive System Diseases::Gastrointestinal Diseases::Gastroenteritis::Inflammatory Bowel Diseases::Crohn Disease</dc:subject>
   <dc:subject>Other subheadings::Other subheadings::Other subheadings::/drug therapy</dc:subject>
   <dc:subject>CHEMICALS AND DRUGS::Chemical Actions and Uses::Pharmacologic Actions::Therapeutic Uses::Anti-Inflammatory Agents</dc:subject>
   <dc:subject>CIENCIA DE LA INFORMACIÓN::Ciencias de la información::metodologías computacionales::algoritmos::inteligencia artificial::aprendizaje automático</dc:subject>
   <dc:subject>ENFERMEDADES::enfermedades del sistema digestivo::enfermedades gastrointestinales::gastroenteritis::enfermedad inflamatoria intestinal::enfermedad de Crohn</dc:subject>
   <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia</dc:subject>
   <dc:subject>COMPUESTOS QUÍMICOS Y DROGAS::acciones y usos químicos::acciones farmacológicas::usos terapéuticos::antiinflamatorios</dc:subject>
   <dcterms:abstract>Malaltia de Crohn; Factors predictius; Ustekinumab</dcterms:abstract>
   <dcterms:abstract>Enfermedad de Crohn; Factores predictivos; Ustekinumab</dcterms:abstract>
   <dcterms:abstract>Crohn’s disease; Predictive factors; Ustekinumab</dcterms:abstract>
   <dcterms:abstract>Ustekinumab has shown efficacy in Crohn’s Disease (CD) patients. To identify patient profiles of those who benefit the most from this treatment would help to position this drug in the therapeutic paradigm of CD and generate hypotheses for future trials. The objective of this analysis was to determine whether baseline patient characteristics are predictive of remission and the drug durability of ustekinumab, and whether its positioning with respect to prior use of biologics has a significant effect after correcting for disease severity and phenotype at baseline using interpretable machine learning. Patients’ data from SUSTAIN, a retrospective multicenter single-arm cohort study, were used. Disease phenotype, baseline laboratory data, and prior treatment characteristics were documented. Clinical remission was defined as the Harvey Bradshaw Index ≤ 4 and was tracked longitudinally. Drug durability was defined as the time until a patient discontinued treatment. A total of 439 participants from 60 centers were included and a total of 20 baseline covariates considered. Less exposure to previous biologics had a positive effect on remission, even after controlling for baseline disease severity using a non-linear, additive, multivariable model. Additionally, age, body mass index, and fecal calprotectin at baseline were found to be statistically significant as independent negative risk factors for both remission and drug survival, with further risk factors identified for remission.</dcterms:abstract>
   <dcterms:abstract>This work was supported by Janssen-Cilag Spain. This sponsor had a partial role in study design, analysis, and interpretation of data.</dcterms:abstract>
   <dcterms:dateAccepted>2025-10-24T10:29:46Z</dcterms:dateAccepted>
   <dcterms:available>2025-10-24T10:29:46Z</dcterms:available>
   <dcterms:created>2025-10-24T10:29:46Z</dcterms:created>
   <dcterms:issued>2022-12-12T13:25:18Z</dcterms:issued>
   <dcterms:issued>2022-12-12T13:25:18Z</dcterms:issued>
   <dcterms:issued>2022-08-03</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>http://hdl.handle.net/11351/8651</dc:identifier>
   <dc:relation>Journal of Clinical Medicine;11(15)</dc:relation>
   <dc:relation>https://doi.org/10.3390/jcm11154518</dc:relation>
   <dc:rights>Attribution 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>MDPI</dc:publisher>
   <dc:source>Scientia</dc:source>
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