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dc.contributor.authorRodriguez-Fontenla, Cristinaes_ES
dc.contributor.authorCalaza, Manueles_ES
dc.contributor.authorEvangelou, Evangeloses_ES
dc.contributor.authorValdés, Ana Mes_ES
dc.contributor.authorArden, Nigeles_ES
dc.contributor.authorBlanco, Francisco Jes_ES
dc.contributor.authorCarr, Andrewes_ES
dc.contributor.authorChapman, Kayes_ES
dc.contributor.authorDeloukas, Panoses_ES
dc.contributor.authorDoherty, Michaeles_ES
dc.contributor.authorEsko, Tonues_ES
dc.contributor.authorGarcés Aleta, Carlos Mariano es_ES
dc.contributor.authorGómez-Reino Carnota, JJes_ES
dc.contributor.authorHelgadottir, Hafdises_ES
dc.contributor.authorHofman, Albertes_ES
dc.contributor.authorJonsdottir, Ingileifes_ES
dc.contributor.authorKerkhof, Hanneke JMes_ES
dc.contributor.authorKloppenburg, Margreetes_ES
dc.contributor.authorMcCaskie, Andrewes_ES
dc.contributor.authorNtzani, Evangelia E.es_ES
dc.contributor.authorRiancho Moral, José Antonio es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2017-01-03T11:35:36Z
dc.date.available2017-01-03T11:35:36Z
dc.date.issued2014es_ES
dc.identifier.issn2326-5205es_ES
dc.identifier.issn2326-5191es_ES
dc.identifier.otherISCIII grants PS09/01431 and PI11/01048,es_ES
dc.identifier.urihttp://hdl.handle.net/10902/9904
dc.description.abstractOBJECTIVE: To assess candidate genes for association with osteoarthritis (OA) and identify promising genetic factors and, secondarily, to assess the candidate gene approach in OA. METHODS: A total of 199 candidate genes for association with OA were identified using Human Genome Epidemiology (HuGE) Navigator. All of their single-nucleotide polymorphisms (SNPs) with an allele frequency of >5% were assessed by fixed-effects meta-analysis of 9 genome-wide association studies (GWAS) that included 5,636 patients with knee OA and 16,972 control subjects and 4,349 patients with hip OA and 17,836 control subjects of European ancestry. An additional 5,921 individuals were genotyped for significantly associated SNPs in the meta-analysis. After correction for the number of independent tests, P values less than 1.58 × 10(-5) were considered significant. RESULTS: SNPs at only 2 of the 199 candidate genes (COL11A1 and VEGF) were associated with OA in the meta-analysis. Two SNPs in COL11A1 showed association with hip OA in the combined analysis: rs4907986 (P = 1.29 × 10(-5) , odds ratio [OR] 1.12, 95% confidence interval [95% CI] 1.06-1.17) and rs1241164 (P = 1.47 × 10(-5) , OR 0.82, 95% CI 0.74-0.89). The sex-stratified analysis also showed association of COL11A1 SNP rs4908291 in women (P = 1.29 × 10(-5) , OR 0.87, 95% CI 0.82-0.92); this SNP showed linkage disequilibrium with rs4907986. A single SNP of VEGF, rs833058, showed association with hip OA in men (P = 1.35 × 10(-5) , OR 0.85, 95% CI 0.79-0.91). After additional samples were genotyped, association at one of the COL11A1 signals was reinforced, whereas association at VEGF was slightly weakened. CONCLUSION: Two candidate genes, COL11A1 and VEGF, were significantly associated with OA in this focused meta-analysis. The remaining candidate genes were not associated.es_ES
dc.format.extent10 p.es_ES
dc.language.isoenges_ES
dc.publisherJohn Wiley and Sons Ltdes_ES
dc.rightsAtribución-NoComercial 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es/*
dc.sourceArthritis Rheumatol. 2014 Apr;66(4):940-9es_ES
dc.titleAssessment of osteoarthritis candidate genes in a meta-analysis of nine genome-wide association studieses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsopenAccesses_ES
dc.type.versionpublishedVersiones_ES


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Atribución-NoComercial 3.0 EspañaExcepto si se señala otra cosa, la licencia del ítem se describe como Atribución-NoComercial 3.0 España