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dc.contributor.authorRodríguez-Fontenla, Cristina
dc.contributor.authorCalaza, Manuel
dc.contributor.authorEvangelou, Evangelos
dc.contributor.authorValdés, Ana M.
dc.contributor.authorArden, Nigel
dc.contributor.authorBlanco García, Francisco J
dc.contributor.authorCarr, Andrew
dc.contributor.authorChapman, Kay
dc.contributor.authorDeloukas, Panos
dc.contributor.authorDoherty, Michael
dc.contributor.authorEsko, Tonu
dc.contributor.authorGarcés Aletá, Carlos M.
dc.contributor.authorGómez-Reino Carnota, Juan J.
dc.contributor.authorHelgadottir, Hafids
dc.contributor.authorHofman, Albert
dc.contributor.authorJonsdottir, Ingilef
dc.contributor.authorKerkhof, Henneke J.M.
dc.contributor.authorKloppenburg, Margreet
dc.contributor.authorMcCaskie, Andrew
dc.contributor.authorNtzani, Evangelia E.
dc.contributor.authorOllier, William E.R.
dc.contributor.authorOreiro, Natividad
dc.contributor.authorPanoutsopoulo, Kalliope
dc.contributor.authorRalston, Stuart H.
dc.contributor.authorRamos, Yolande F. M.
dc.contributor.authorRiancho, José A.
dc.contributor.authorRivadeneira, Fernando
dc.contributor.authorSlagboom, Eline
dc.contributor.authorStyrkarsdottir, Unnur
dc.contributor.authorThorsteindottir, Unnur
dc.contributor.authorThorleifsson, Gudmar
dc.contributor.authorTsezou, Aspasia
dc.contributor.authorUitterlinden, André G.
dc.contributor.authorWallis, Gillian A.
dc.contributor.authorWilkinson, J. Mark
dc.contributor.authorZhai, Yanyan
dc.contributor.authorFelson, David T.
dc.contributor.authorIoannidis, John P.A.
dc.contributor.authorLoughlin, John
dc.contributor.authorMetspalu, Andres
dc.contributor.authorMeulenbelt, Ingrid
dc.contributor.authorStefansson, Kari
dc.contributor.authorvan Meurs, Joyce B.
dc.contributor.authorZeggini, Eleftheria
dc.contributor.authorSpector, Timothy D.
dc.contributor.authorGonzález, Antonio
dc.date.accessioned2020-07-02T09:44:06Z
dc.date.available2020-07-02T09:44:06Z
dc.date.issued2013-12-10
dc.identifier.citationRodríguez-Fontenla C, Calaza M, Evangelou E, Valdés AM, Arden N, Blanco FJ, et al. Assessment of osteoarthritis candidate genes in a meta-analysis of nine genome-wide association studies. Arthritis Rheumatol. 2014;66(4):940-949es_ES
dc.identifier.issn2326-5191
dc.identifier.urihttp://hdl.handle.net/2183/25864
dc.description.abstract[Abstract] Objective: 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.description.sponsorshipInstituto de Salud Carlos III; PS09/01431es_ES
dc.description.sponsorshipInstituto de Salud Carlos III; PI11/01048es_ES
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.relation.urihttps://doi.org/10.1002/art.38300es_ES
dc.rightsAtribución 4.0 Españaes_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/es/*
dc.subjectCollagen type XIes_ES
dc.subjectGene fraquencyes_ES
dc.subjectGenetic predisposition to diseasees_ES
dc.subjectGenome wide association studyes_ES
dc.subjectGenotypees_ES
dc.subjectOsteoarthritis-Hipes_ES
dc.subjectOsteoarthritis-Kneees_ES
dc.subjectPolymorphism-Single nucleotidees_ES
dc.subjectVascular endothelial growth factor Aes_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.accessinfo:eu-repo/semantics/openAccesses_ES
UDC.journalTitleArthritis and Rheumatologyes_ES
UDC.volume66es_ES
UDC.issue4es_ES
UDC.startPage940es_ES
UDC.endPage949es_ES


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