<?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>2026-04-17T04:30:54Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:11351/5958" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:11351/5958</identifier><datestamp>2025-10-24T10:42:30Z</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>Whole Transcription Profile of Responders to Anti-TNF Drugs in Pediatric Inflammatory Bowel Disease</dc:title>
   <dc:creator>Kaczmarczyk, Bartosz</dc:creator>
   <dc:creator>Álvarez, Rebeca</dc:creator>
   <dc:creator>Navas-López, Víctor Manuel</dc:creator>
   <dc:creator>Gallego-Fernández, Carmen</dc:creator>
   <dc:creator>Moreno-Álvarez, Ana</dc:creator>
   <dc:creator>Clemente Bautista, Susana</dc:creator>
   <dc:creator>Salvador-Martín, Sara</dc:creator>
   <dc:subject>Intestins - Inflamació</dc:subject>
   <dc:subject>Medicaments - Administració</dc:subject>
   <dc:subject>Adolescents</dc:subject>
   <dc:subject>DISEASES::Digestive System Diseases::Gastrointestinal Diseases::Gastroenteritis::Inflammatory Bowel Diseases</dc:subject>
   <dc:subject>Other subheadings::Other subheadings::Other subheadings::/drug therapy</dc:subject>
   <dc:subject>NAMED GROUPS::Persons::Age Groups::Adolescent</dc:subject>
   <dc:subject>ENFERMEDADES::enfermedades del sistema digestivo::enfermedades gastrointestinales::gastroenteritis::enfermedad inflamatoria intestinal</dc:subject>
   <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia</dc:subject>
   <dc:subject>DENOMINACIONES DE GRUPOS::personas::Grupos de Edad::adolescente</dc:subject>
   <dcterms:abstract>Biomarcador; Expressió gènica; Malaltia inflamatòria intestinal</dcterms:abstract>
   <dcterms:abstract>Biomarcador; Expresión génica; Enfermedad inflamatoria intestinal</dcterms:abstract>
   <dcterms:abstract>Biomarker; Gene expression; Inflammatory bowel disease</dcterms:abstract>
   <dcterms:abstract>Background: Up to 30% of patients with pediatric inflammatory bowel disease (IBD) do not respond to anti-Tumor Necrosis Factor (anti-TNF) therapy. The aim of this study was to identify pharmacogenomic markers that predict early response to anti-TNF drugs in pediatric patients with IBD. Methods: An observational, longitudinal, prospective cohort study was conducted. The study population comprised 38 patients with IBD aged &lt; 18 years who started treatment with infliximab or adalimumab (29 responders and nine non-responders). Whole gene expression profiles from total RNA isolated from whole blood samples of six responders and six non-responders taken before administration of the biologic and after two weeks of therapy were analyzed using next-generation RNA sequencing. The expression of six selected genes was measured for purposes of validation in all of the 38 patients recruited using qPCR. Results: Genes were differentially expressed in non-responders and responders (32 before initiation of treatment and 44 after two weeks, Log2FC (Fold change) >0.6 or &lt;−0.6 and p value &lt; 0.05). After validation, FCGR1A, FCGR1B, and GBP1 were overexpressed in non-responders two weeks after initiation of anti-TNF treatment (Log2FC 1.05, 1.21, and 1.08, respectively, p value &lt; 0.05). Conclusion: Expression of the FCGR1A, FCGR1B, and GBP1 genes is a pharmacogenomic biomarker of early response to anti-TNF agents in pediatric IBD.</dcterms:abstract>
   <dcterms:abstract>This research was funded by Instituto de Salud Carlos III (grants numbers PI16/00559 and PI19/00792), Consejería de Educación y Deporte de la Comunidad de Madrid (grant number PEJ16/MED/AI-1260), and by the Gregorio Marañón Health Research Institute (grant number PRE-2018-2). The study was cofunded by European Regional Develompment Funds (FEDER) from the European Commission, “A way of making Europe”.</dcterms:abstract>
   <dcterms:dateAccepted>2025-10-24T10:42:30Z</dcterms:dateAccepted>
   <dcterms:available>2025-10-24T10:42:30Z</dcterms:available>
   <dcterms:created>2025-10-24T10:42:30Z</dcterms:created>
   <dcterms:issued>2021-05-17T12:17:43Z</dcterms:issued>
   <dcterms:issued>2021-05-17T12:17:43Z</dcterms:issued>
   <dcterms:issued>2021-01-08</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/11351/5958</dc:identifier>
   <dc:relation>Pharmaceutics;13(1)</dc:relation>
   <dc:relation>https://doi.org/10.3390/pharmaceutics13010077</dc:relation>
   <dc:relation>info:eu-repo/grantAgreement/ES/PE2013-2016/PI16%2F00559</dc:relation>
   <dc:relation>info:eu-repo/grantAgreement/ES/PE2017-2020/PI19%2F00792</dc:relation>
   <dc:relation>info:eu-repo/grantAgreement/ES/PE2013-2016/PEJ16%2FMED%2FAI-1260</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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