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dc.contributor.authorAlonso Sarasquete, María Eugenia
dc.contributor.authorGarcía Sanz, Ramón 
dc.contributor.authorMarín Rubio, Luis Alberto
dc.contributor.authorAlcoceba Sánchez, Miguel 
dc.contributor.authorChillón Santos, María del Carmen
dc.contributor.authorBalanzategui, A
dc.contributor.authorSantamaria, Carlos
dc.contributor.authorRosiñol, Laura
dc.contributor.authorDe la Rubia, Javier
dc.contributor.authorHernandez, Miguel T.
dc.contributor.authorGarcia-Navarro, Inmaculada
dc.contributor.authorLahuerta, Juan José
dc.contributor.authorGonzález Díaz, Marcos 
dc.contributor.authorSan Miguel Izquierdo, Jesús Fernando
dc.date.accessioned2024-02-02T15:59:47Z
dc.date.available2024-02-02T15:59:47Z
dc.date.issued2008-10-01
dc.identifier.citationSarasquete, M. E., García-Sanz, R., Marin, L., Alcoceba, M., Chillón, M. C., Balanzategui, A., ... & San Miguel, J. F. (2008). Bisphosphonate-related osteonecrosis of the jaw is associated with polymorphisms of the cytochrome P450 CYP2C8 in multiple myeloma: a genome-wide single nucleotide polymorphism analysis. Blood, The Journal of the American Society of Hematology, 112(7), 2709-2712. https://doi.org/10.1182/blood-2008-04-147884es_ES
dc.identifier.issn0006-4971
dc.identifier.urihttp://hdl.handle.net/10366/155234
dc.descriptionSe trata de un descubrimiento de gran originalidad que liga la estructura del gen CYP2C8 y la fisiopatología dentaria como causa de osteonecrosis de mandíbula en pacientes bajo trata-miento con bisfosfonatos. Es uno de los verdaderos avances de la tecnología d SNPs en los denominados GWAS (Genomic Wide Association Studies, o estudios de asociación genética ampliada)es_ES
dc.description.abstract[EN]We have explored the potential role of genetics in the development of osteonecrosis of the jaw (ONJ) in multiple myeloma (MM) patients under bisphosphonate therapy. A genome-wide association study was performed using 500 568 single nucleotide polymorphisms (SNPs) in 2 series of homogeneously treated MM patients, one with ONJ (22 MM cases) and another without ONJ (65 matched MM controls). Four SNPs (rs1934951, rs1934980, rs1341162, and rs17110453) mapped within the cytochrome P450-2C gene (CYP2C8) showed a different distribution between cases and controls with statistically significant differences (P = 1.07 x 10(-6), P = 4.231 x 10(-6), P = 6.22 x 10(-6), and P = 2.15 x 10(-6), respectively). SNP rs1934951 was significantly associated with a higher risk of ONJ development even after Bonferroni correction (P corrected value = .02). Genotyping results displayed an overrepresentation of the T allele in cases compared with controls (48% vs 12%). Thus, individuals homozygous for the T allele had an increased likelihood of developing ONJ (odds ratio 12.75, 95% confidence interval 3.7-43.5).es_ES
dc.description.sponsorshipHospital Universitario de Salamanca Universidad de Salamancaes_ES
dc.language.isoenges_ES
dc.publisherAmerican Society of Hematologyes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectBisphosphonatees_ES
dc.subjectOsteonecrosis of the Jawes_ES
dc.subjectMyelomaes_ES
dc.subjectGenetic Polymorphismses_ES
dc.subject.meshGenetic Predisposition to Disease *
dc.subject.meshDiphosphonates *
dc.subject.meshJaw Diseases *
dc.subject.meshMultiple Myeloma *
dc.subject.meshAlleles *
dc.subject.meshHaplotypes *
dc.subject.meshHumans *
dc.subject.meshGenome *
dc.subject.meshOsteonecrosis *
dc.subject.meshAryl Hydrocarbon Hydroxylases *
dc.titleBisphosphonate-related osteonecrosis of the jaw is associated with polymorphisms of the cytochrome P450 CYP2C8 in multiple myeloma: a genome-wide single nucleotide polymorphism analysises_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1182/blood-2008-04-147884es_ES
dc.subject.unesco3205.04 Hematologíaes_ES
dc.identifier.doi10.1182/blood-2008-04-147884
dc.relation.projectIDPI06-1354es_ES
dc.relation.projectIDRed Española de Cancer RD06/0020/0006es_ES
dc.relation.projectIDIDIBAPSes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.pmid18594024
dc.identifier.essn1528-0020
dc.journal.titleBloodes_ES
dc.volume.number112es_ES
dc.issue.number7es_ES
dc.page.initial2709es_ES
dc.page.final2712es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decsalelos *
dc.subject.decsdifosfonatos *
dc.subject.decsaril hidrocarburo hidroxilasas *
dc.subject.decshumanos *
dc.subject.decsenfermedades maxilomandibulares *
dc.subject.decsmieloma múltiple *
dc.subject.decsosteonecrosis *
dc.subject.decsgenoma *
dc.subject.decshaplotipos *
dc.subject.decspredisposición genética a la enfermedad *
dc.description.projectHospital Universitario de Salamancaes_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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