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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorKaczmarczyk, Bartosz
dc.contributor.authorÁlvarez, Rebeca
dc.contributor.authorNavas-López, Víctor Manuel
dc.contributor.authorGallego-Fernández, Carmen
dc.contributor.authorMoreno-Álvarez, Ana
dc.contributor.authorClemente Bautista, Susana
dc.contributor.authorSalvador-Martín, Sara
dc.date.accessioned2021-05-17T12:17:43Z
dc.date.available2021-05-17T12:17:43Z
dc.date.issued2021-01-08
dc.identifier.citationSalvador-Martín S, Kaczmarczyk B, Álvarez R, Navas-López VM, Gallego-Fernández C, Moreno-Álvarez A, et al. Whole Transcription Profile of Responders to Anti-TNF Drugs in Pediatric Inflammatory Bowel Disease. Pharmaceutics. 2021 Jan 8;13(1):77.
dc.identifier.issn1999-4923
dc.identifier.urihttps://hdl.handle.net/11351/5958
dc.descriptionBiomarker; Gene expression; Inflammatory bowel disease
dc.description.abstractBackground: 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 < 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 <−0.6 and p value < 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 < 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.
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofseriesPharmaceutics;13(1)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectIntestins - Inflamació
dc.subjectMedicaments - Administració
dc.subjectAdolescents
dc.subject.meshInflammatory Bowel Diseases
dc.subject.mesh/drug therapy
dc.subject.meshAdolescent
dc.titleWhole Transcription Profile of Responders to Anti-TNF Drugs in Pediatric Inflammatory Bowel Disease
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3390/pharmaceutics13010077
dc.subject.decsenfermedad inflamatoria intestinal
dc.subject.decs/farmacoterapia
dc.subject.decsadolescente
dc.relation.publishversionhttps://doi.org/10.3390/pharmaceutics13010077
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Salvador-Martín S, Kaczmarczyk B] Pharmacy Department, Instituto de Investigación Sanitaria Gregorio Marañón, Hospital General Universitario Gregorio Marañón, 28007 Madrid, Spain. [Álvarez R] Genomics Unit, Spanish Nacional Center for Cardiovascular Diseases (CNIC), 28029 Madrid, Spain. [Navas-López VM] Pediatric Gastroenterology and Nutrition Unit, Hospital Regional Universitario de Málaga, IBIMA Multidisciplinary Group for Pediatric Research, 29010 Málaga, Spain. [Gallego-Fernández C] Pharmacy Department, Hospital Regional Universitario de Málaga, 29010 Málaga, Spain. [Moreno-Álvarez A] Pediatric Gastroenterology Unit, Department of Pediatrics, A Coruña University Hospital, 15006 A Coruña, Spain. [Clemente S] Servei de Farmàcia, Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid33429950
dc.identifier.wos000610704100001
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2013-2016/PI16%2F00559
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2017-2020/PI19%2F00792
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2013-2016/PEJ16%2FMED%2FAI-1260
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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