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dc.contributor.authorSalvador-Martín, S.*
dc.contributor.authorZapata-Cobo, P.*
dc.contributor.authorVelasco, M.*
dc.contributor.authorPalomino, L.M.*
dc.contributor.authorClemente, S.*
dc.contributor.authorSegarra, O.*
dc.contributor.authorSánchez, C.*
dc.contributor.authorTolín, M.*
dc.contributor.authorMoreno Alvarez, Ana *
dc.contributor.authorFernández Lorenzo, Ana Estefanía*
dc.contributor.authorPérez-Moneo, B.*
dc.contributor.authorLoverdos, I.*
dc.contributor.authorNavas López, V.M.*
dc.contributor.authorMillán, A.*
dc.contributor.authorMagallares, L.*
dc.contributor.authorTorres-Peral, R.*
dc.contributor.authorGarcía-Romero, R.*
dc.contributor.authorPujol-Muncunill, G.*
dc.contributor.authorMerino-Bohorquez, V.*
dc.contributor.authorRodríguez, A.*
dc.contributor.authorSalcedo, E.*
dc.contributor.authorLópez-Cauce, B.*
dc.contributor.authorMarín-Jiménez, I.*
dc.contributor.authorMenchén, L.*
dc.contributor.authorLaserna-Mendieta, E.*
dc.contributor.authorLucendo, A.J.*
dc.contributor.authorSanjurjo-Sáez, M.*
dc.contributor.authorLópez-Fernández, L.A.*
dc.date.accessioned2025-09-08T09:17:15Z
dc.date.available2025-09-08T09:17:15Z
dc.date.issued2023
dc.identifier.citationSalvador-Martín S, Zapata-Cobo P, Velasco M, Palomino LM, Clemente S, Segarra O, et al. Association between HLA DNA Variants and Long-Term Response to Anti-TNF Drugs in a Spanish Pediatric Inflammatory Bowel Disease Cohort. International Journal of Molecular Sciences. 2023;24(2).
dc.identifier.issn1422-0067
dc.identifier.otherhttps://portalcientifico.sergas.gal//documentos/63df0a7c6fdec82c4e7dec36
dc.identifier.urihttp://hdl.handle.net/20.500.11940/21115
dc.description.abstractThe genetic polymorphisms rs2395185 and rs2097432 in HLA genes have been associated with the response to anti-TNF treatment in inflammatory bowel disease (IBD). The aim was to analyze the association between these variants and the long-term response to anti-TNF drugs in pediatric IBD. We performed an observational, multicenter, ambispective study in which we selected 340 IBD patients under 18 years of age diagnosed with IBD and treated with anti-TNF drugs from a network of Spanish hospitals. Genotypes and failure of anti-TNF drugs were analyzed using Kaplan-Meier curves and Cox logistic regression. The homozygous G allele of rs2395185 and the C allele of rs2097432 were associated with impaired long-term response to anti-TNF drugs in children with IBD after 3 and 9 years of follow-up. Being a carrier of both polymorphisms increased the risk of anti-TNF failure. The SNP rs2395185 but not rs2097432 was associated with response to infliximab in adults with CD treated with infliximab but not in children after 3 or 9 years of follow-up. Conclusions: SNPs rs2395185 and rs2097432 were associated with a long-term response to anti-TNFs in IBD in Spanish children. Differences between adults and children were observed in patients diagnosed with CD and treated with infliximab.
dc.description.sponsorshipThis research was funded by Instituto de Salud Carlos III, grant number PI19/00792 (L.A.L.-F.) and Juan Rodes program JR19/00005 (E.L.-M.), by Instituto de Investigacion Sanitaria Gregorio Maranon, grant number 2021-II-postdoc-01 (S.S.-M.), and by Consejeria de Educacion, Universidades, Ciencia y Portavocia Comunidad de Madrid, grant number PEJ-2021-AI/BMD-21866 (P.Z.-C.). The study was co-funded by the European Union.
dc.languageeng
dc.rightsAttribution 4.0 International (CC BY 4.0)*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshAdult *
dc.subject.meshHumans *
dc.subject.meshChild *
dc.subject.meshAdolescent *
dc.subject.meshInfliximab *
dc.subject.meshAdalimumab *
dc.subject.meshTumor Necrosis Factor Inhibitors *
dc.subject.meshTumor Necrosis Factor-alpha *
dc.subject.meshInflammatory Bowel Diseases *
dc.subject.meshPolymorphism, Single Nucleotide*
dc.subject.meshDNA *
dc.subject.meshRetrospective Studies *
dc.titleAssociation between HLA DNA Variants and Long-Term Response to Anti-TNF Drugs in a Spanish Pediatric Inflammatory Bowel Disease Cohort
dc.typeArtigo
dc.authorsophosSalvador-Martín, S.; Zapata-Cobo, P.; Velasco, M.; Palomino, L.M.; Clemente, S.; Segarra, O.; Sánchez, C.; Tolín, M.; Moreno-Álvarez, A.; Fernández-Lorenzo, A.; Pérez-Moneo, B.; Loverdos, I.; Navas López, V.M.; Millán, A.; Magallares, L.; Torres-Peral, R.; García-Romero, R.; Pujol-Muncunill, G.; Merino-Bohorquez, V.; Rodríguez, A.; Salcedo, E.; López-Cauce, B.; Marín-Jiménez, I.; Menchén, L.; Laserna-Mendieta, E.; Lucendo, A.J.; Sanjurjo-Sáez, M.; López-Fernández, L.A.
dc.identifier.doi10.3390/ijms24021797
dc.identifier.sophos63df0a7c6fdec82c4e7dec36
dc.issue.number2
dc.journal.titleInternational Journal of Molecular Sciences*
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario A Coruña::Pediatría
dc.organizationComplexo Hospitalario Universitario A Coruña
dc.relation.projectIDInstituto de Salud Carlos III [PI19/00792, JR19/00005]
dc.relation.projectIDInstituto de Investigacion Sanitaria Gregorio Maranon [2021-II-postdoc-01]
dc.relation.projectIDConsejeria de Educacion, Universidades, Ciencia y Portavocia Comunidad de Madrid [PEJ-2021-AI/BMD-21866]
dc.relation.projectIDEuropean Union
dc.relation.publisherversionhttps://doi.org/10.3390/ijms24021797
dc.rights.accessRightsopenAccess*
dc.subject.keywordAS A Coruña
dc.subject.keywordCHUAC
dc.subject.keywordCHUAC
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)
dc.typesophosArtículo Original
dc.volume.number24


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Attribution 4.0 International (CC BY 4.0)
Excepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International (CC BY 4.0)