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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorZapata-Cobo, Paula
dc.contributor.authorSalvador-Martín, Sara
dc.contributor.authorVelasco, Marta
dc.contributor.authorPalomino Pérez, Laura María
dc.contributor.authorClemente, Susana
dc.contributor.authorSegarra, Oscar
dc.date.accessioned2023-08-23T07:16:24Z
dc.date.available2023-08-23T07:16:24Z
dc.date.issued2023-08
dc.identifier.citationZapata-Cobo P, Salvador-Martín S, Velasco M, Palomino LM, Clemente S, Segarra O, et al. Polymorphisms indicating risk of inflammatory bowel disease or antigenicity to anti-TNF drugs as biomarkers of response in children. Pharmacol Res. 2023 Aug;194:106859.
dc.identifier.issn1043-6618
dc.identifier.urihttps://hdl.handle.net/11351/10128
dc.descriptionCrohn’s disease; Polymorphism; Pediatric
dc.description.abstractFew genetic polymorphisms predict early response to anti-TNF drugs in inflammatory bowel disease (IBD), and even fewer have been identified in the pediatric population. However, it would be of considerable clinical interest to identify and validate genetic biomarkers of long-term response. Therefore, the aim of the study was to analyze the usefulness of biomarkers of response to anti-TNFs in pediatric IBD (pIBD) as long-term biomarkers and to find differences by type of IBD and type of anti-TNF drug. The study population comprised 340 children diagnosed with IBD who were treated with infliximab or adalimumab. Genotyping of 9 selected SNPs for their association with early response and/or immunogenicity to anti-TNFs was performed using real-time PCR. Variants C rs10508884 (CXCL12), A rs2241880 (ATG16L1), and T rs6100556 (PHACTR3) (p value 0.049; p value 0.03; p value 0.031) were associated with worse long-term response to anti-TNFs in pIBD. DNA variants specific to disease type and anti-TNF type were identified in the pediatric population. Genotyping of these genetic variants before initiation of anti-TNFs would enable, if validated in a prospective cohort, the identification of pediatric patients who are long-term responders to this therapy.
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesPharmacological Research;194
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectIntestins - Inflamació - Tractament
dc.subjectFactor de necrosi tumoral - Inhibidors - Ús terapèutic
dc.subject.meshInflammatory Bowel Diseases
dc.subject.mesh/drug therapy
dc.subject.meshTumor Necrosis Factors
dc.subject.mesh/antagonists & inhibitors
dc.titlePolymorphisms indicating risk of inflammatory bowel disease or antigenicity to anti-TNF drugs as biomarkers of response in children
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.phrs.2023.106859
dc.subject.decsenfermedad inflamatoria intestinal
dc.subject.decs/farmacoterapia
dc.subject.decsfactores de necrosis tumoral
dc.subject.decs/antagonistas & inhibidores
dc.relation.publishversionhttps://doi.org/10.1016/j.phrs.2023.106859
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Zapata-Cobo P, Salvador-Martín S] Instituto de Investigación Sanitaria Gregorio Marañón, Hospital General Universitario Gregorio Marañón, Madrid, Spain. [Velasco M, Palomino LM] Hospital Universitario Infantil Niño Jesús, Madrid, Spain. [Clemente S, Segarra O] Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid37473877
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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