Mostrar el registro sencillo del ítem

dc.contributor.authorEvangelou, Evangelos
dc.contributor.authorKerkhof, Hanneke J.M
dc.contributor.authorStyrkarsdottir, Unnur
dc.contributor.authorNtzani, Evangelia E
dc.contributor.authorBos, Steffan D
dc.contributor.authorEsko, Tonu
dc.contributor.authorEvans, Daniel S
dc.contributor.authorMetrustry, Sarah
dc.contributor.authorPanoutsopoulou, Kalliope
dc.contributor.authorRamos, Yolande F M
dc.contributor.authorThorleifsson, Gudmar
dc.contributor.authorTsilidis, Konstantinos K
dc.contributor.authorArden, Nigel
dc.contributor.authorAslam, Nadim
dc.contributor.authorBellamy, Nicholas
dc.contributor.authorBirrell, Fraser
dc.contributor.authorBLANCO GARCIA, FRANCISCO JAVIER 
dc.contributor.authorCarr, Andrew
dc.contributor.authorChapman, Kay
dc.contributor.authorDay-Williams, Aaron G
dc.contributor.authorDeloukas, Panos
dc.contributor.authorDoherty, Michael
dc.contributor.authorEngström, Gunnar
dc.contributor.authorHelgadottir, Hafdis T
dc.contributor.authorHofman, Albert
dc.contributor.authorIngvarsson, Thorvaldur
dc.contributor.authorJonsson, Helgi
dc.contributor.authorKeis, Aime
dc.contributor.authorKeurentjes, J Christiaan
dc.contributor.authorKloppenburg, Margreet
dc.contributor.authorLind, Penelope A
dc.contributor.authorMcCaskie, Andrew
dc.contributor.authorMartin, Nicholas G
dc.contributor.authorMilani, Lili
dc.contributor.authorMontgomery, Grant W
dc.contributor.authorNelissen, Rob G H H
dc.contributor.authorNevitt, Michael C
dc.contributor.authorNilsson, Peter M
dc.contributor.authorOllier, William Er
dc.contributor.authorParimi, Neeta
dc.contributor.authorRai, Ashok
dc.contributor.authorRalston, Stuart H
dc.contributor.authorReed, Mike R
dc.contributor.authorRiancho, Jose A
dc.contributor.authorRivadeneira, Fernando
dc.contributor.authorRodríguez Fontenla, Cristina
dc.contributor.authorSoutham, Lorraine
dc.contributor.authorThorsteinsdottir, Unnur
dc.contributor.authorTsezou, Aspasia
dc.contributor.authorWallis, Gillian A
dc.contributor.authorWilkinson, J Mark
dc.contributor.authorGonzález Martínez-Pedrayo, Antonio 
dc.contributor.authorLane, Nancy E
dc.contributor.authorLohmander, L Stefan
dc.contributor.authorLoughlin, John
dc.contributor.authorMetspalu, Andres
dc.contributor.authorUitterlinden, Andre G
dc.contributor.authorJonsdottir, Ingileif
dc.contributor.authorStefansson, Kari
dc.contributor.authorSlagboom, P Eline
dc.contributor.authorZeggini, Eleftheria
dc.contributor.authorMeulenbelt, Ingrid
dc.contributor.authorIoannidis, John Pa
dc.contributor.authorSpector, Tim D
dc.contributor.authorvan Meurs, Joyce B J
dc.contributor.authorValdes, Ana M
dc.date.accessioned2017-06-07T07:16:20Z
dc.date.available2017-06-07T07:16:20Z
dc.date.issued2014
dc.identifier.issn0003-4967
dc.identifier.urihttp://hdl.handle.net/20.500.11940/4576
dc.description.abstractObjectives: Osteoarthritis (OA) is the most common form of arthritis with a clear genetic component. To identify novel loci associated with hip OA we performed a meta-analysis of genome-wide association studies (GWAS) on European subjects. Methods: We performed a two-stage meta-analysis on more than 78,000 participants. In stage 1, we synthesised data from eight GWAS whereas data from 10 centres were used for 'in silico' or 'de novo' replication. Besides the main analysis, a stratified by sex analysis was performed to detect possible sex-specific signals. Meta-analysis was performed using inverse-variance fixed effects models. A random effects approach was also used. Results: We accumulated 11,277 cases of radiographic and symptomatic hip OA. We prioritised eight single nucleotide polymorphism (SNPs) for follow-up in the discovery stage (4349 OA cases); five from the combined analysis, two male specific and one female specific. One locus, at 20q13, represented by rs6094710 (minor allele frequency (MAF) 4%) near the NCOA3 (nuclear receptor coactivator 3) gene, reached genome-wide significance level with p=7.9×10(-9) and OR=1.28 (95% CI 1.18 to 1.39) in the combined analysis of discovery (p=5.6×10(-8)) and follow-up studies (p=7.3×10(-4)). We showed that this gene is expressed in articular cartilage and its expression was significantly reduced in OA-affected cartilage. Moreover, two loci remained suggestive associated; rs5009270 at 7q31 (MAF 30%, p=9.9×10(-7), OR=1.10) and rs3757837 at 7p13 (MAF 6%, p=2.2×10(-6), OR=1.27 in male specific analysis). Conclusions: Novel genetic loci for hip OA were found in this meta-analysis of GWAS.
dc.language.isoeng
dc.rightsAtribución 4.0
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshOsteoarthritis, Hip
dc.subject.meshGene Frequency
dc.subject.meshCalcium-Calmodulin-Dependent Protein Kinase Type 2
dc.subject.meshEuropean Continental Ancestry Group
dc.subject.meshGenetic Predisposition to Disease
dc.subject.meshGenome-Wide Association Study
dc.titleA meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip
dc.typeArtigoes
dc.contributor.authorcorparcOGEN Consortium
dc.authorsophosEvangelou, E.
dc.authorsophosKerkhof, H. J.
dc.authorsophosStyrkarsdottir, U.
dc.authorsophosNtzani, E. E.
dc.authorsophosBos, S. D.
dc.authorsophosEsko, T.
dc.authorsophosEvans, D. S.
dc.authorsophosMetrustry, S.
dc.authorsophosPanoutsopoulou, K.
dc.authorsophosRamos, Y. F.
dc.authorsophosThorleifsson, G.
dc.authorsophosTsilidis, K. K.
dc.authorsophosArden, N.
dc.authorsophosAslam, N.
dc.authorsophosBellamy, N.
dc.authorsophosBirrell, F.
dc.authorsophosBlanco, F. J.
dc.authorsophosCarr, A.
dc.authorsophosChapman, K.
dc.authorsophosDay-Williams, A. G.
dc.authorsophosDeloukas, P.
dc.authorsophosDoherty, M.
dc.authorsophosEngström, G.
dc.authorsophosHelgadottir, H. T.
dc.authorsophosHofman, A.
dc.authorsophosIngvarsson, T.
dc.authorsophosJonsson, H.
dc.authorsophosKeis, A.
dc.authorsophosKeurentjes, J. C.
dc.authorsophosKloppenburg, M.
dc.authorsophosLind, P. A.
dc.authorsophosMcCaskie, A.
dc.authorsophosMartin, N. G.
dc.authorsophosMilani, L.
dc.authorsophosMontgomery, G. W.
dc.authorsophosNelissen, R. G.
dc.authorsophosNevitt, M. C.
dc.authorsophosNilsson, P. M.
dc.authorsophosOllier, W. E.
dc.authorsophosParimi, N.
dc.authorsophosRai, A.
dc.authorsophosRalston, S. H.
dc.authorsophosReed, M. R.
dc.authorsophosRiancho, J. A.
dc.authorsophosRivadeneira, F.
dc.authorsophosRodriguez-Fontenla, C.
dc.authorsophosSoutham, L.
dc.authorsophosThorsteinsdottir, U.
dc.authorsophosTsezou, A.
dc.authorsophosWallis, G. A.
dc.authorsophosWilkinson, J. M.
dc.authorsophosGonzalez, A.
dc.authorsophosLane, N. E.
dc.authorsophosLohmander, L. S.
dc.authorsophosLoughlin, J.
dc.authorsophosMetspalu, A.
dc.authorsophosUitterlinden, A. G.
dc.authorsophosJonsdottir, I.
dc.authorsophosStefansson, K.
dc.authorsophosSlagboom, P. E.
dc.authorsophosZeggini, E.
dc.authorsophosMeulenbelt, I.
dc.authorsophosIoannidis, J. P.
dc.authorsophosSpector, T. D.
dc.authorsophosvan Meurs, J. B.
dc.authorsophosValdes, A. M.
dc.authorsophosConsortium, arcOGEN
dc.identifier.doi10.1136/annrheumdis-2012-203114
dc.identifier.isi344783900016
dc.identifier.pmid23989986
dc.identifier.sophos14646
dc.issue.number12
dc.journal.titleAnnals of the rheumatic diseases
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de A Coruña - Complexo Hospitalario Universitario A Coruña::Reumatoloxía
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago - Complexo Hospitalario Universitario de Santiago::Reumatoloxía
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago::IDIS.- Instituto de investigaciones sanitarias de Santiago
dc.page.initial2130
dc.page.final6
dc.rights.accessRightsopenAccess
dc.subject.decsOsteoartritis de la Cadera
dc.subject.decsFrecuencia de los Genes
dc.subject.decsProteína Quinasa Tipo 2 Dependiente de Calcio Calmodulina
dc.subject.decsGrupo de Ascendencia Continental Europea
dc.subject.decsPredisposición Genética a la Enfermedad
dc.subject.decsEstudio de Asociación del Genoma Completo
dc.typesophosArtículo Original
dc.volume.number73


Ficheros en el ítem

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem

Atribución 4.0
Excepto si se señala otra cosa, la licencia del ítem se describe como Atribución 4.0