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dc.contributor.authorNuñez Fernandez, Lucia
dc.contributor.authorMarron Liñares, Grecia
dc.contributor.authorCrespo Leiro, Marisa 
dc.contributor.authorBarge Caballero, Eduardo 
dc.contributor.authorAlvarez López, Eloy
dc.contributor.authorSuárez Fuentetaja, Natalia 
dc.contributor.authorPaniagua Martín, María Jesús 
dc.contributor.authorPombo Otero, Jorge 
dc.contributor.authorMuñiz García, Javier 
dc.contributor.authorTan, Carmela D
dc.contributor.authorRodriguez, E Rene
dc.contributor.authorVázquez Rodríguez, José Manuel 
dc.contributor.authorHermida Prieto, Manuel
dc.date.accessioned2022-01-25T12:17:27Z
dc.date.available2022-01-25T12:17:27Z
dc.date.issued2019
dc.identifier.issn1932-6203
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6650139/pdf/pone.0219345.pdfes
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/31335901es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/15922
dc.description.abstractINTRODUCTION: One of the main problems involved in heart transplantation (HT) is antibody-mediated rejection (AMR). Many aspects of AMR are still unresolved, including its etiology, diagnosis and treatment. In this project, we hypothesize that variants in genes involved in B-cell biology in HT patients can yield diagnostic and prognostic information about AMR. METHODS: Genetic variants in 61 genes related to B-cell biology were analyzed by next generation sequencing in 46 HT patients, 23 with and 23 without AMR. RESULTS: We identified 3 single nucleotide polymorphisms in ITGA4 gene (c.1845G>A, c.2633A>G, and c.2883C>T) that conformed the haplotype AGT-ITGA4. This haplotype is associated with the development of AMR. Moreover, AMR patients with the haplotype AGT-ITGA4 present lower levels of integrin alpha-4 in serum samples compared to the reference GAC haplotype in control patients. CONCLUSION: We can conclude that polymorphisms in genes related to the biology of B-cells could have an important role in the development of AMR. In fact, the AGT haplotype in ITGA4 gene could potentially increase the risk of AMR.en
dc.language.isoenges
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshIntegrins*
dc.subject.meshMiddle Aged*
dc.subject.meshHumans*
dc.subject.meshAntibodies*
dc.subject.meshHaplotypes*
dc.subject.meshHeart Transplantation*
dc.subject.meshComputer Simulation*
dc.subject.meshHigh-Throughput Nucleotide Sequencing*
dc.subject.meshGenetic Predisposition to Disease*
dc.subject.meshGraft Rejection*
dc.titleAGT haplotype in ITGA4 gene is related to antibody-mediated rejection in heart transplant patientsen
dc.typeArtigoes
dc.identifier.doi10.1371/journal.pone.0219345
dc.identifier.pmid31335901
dc.identifier.sophos32382
dc.issue.number7es
dc.journal.titlePLoS Onees
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de A Coruña - Complexo Hospitalario Universitario de A Coruña:: Anatomía Patolóxicaes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de A Coruña - Complexo Hospitalario Universitario de A Coruña:: Cardioloxíaes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::Instituto de Investigación Biomédica da Coruña (INIBIC)es
dc.rights.accessRightsopenAccesses
dc.subject.decsintegrinas*
dc.subject.decssecuenciación de nucleótidos de alto rendimiento*
dc.subject.decstrasplante de corazón*
dc.subject.decsmediana edad*
dc.subject.decshumanos*
dc.subject.decshaplotipos*
dc.subject.decsanticuerpos*
dc.subject.decsrechazo del injerto*
dc.subject.decssimulación por ordenador*
dc.subject.decspredisposición genética a la enfermedad*
dc.subject.keywordCHUACes
dc.subject.keywordINIBICes
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number14es


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Atribución 4.0 Internacional
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