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dc.contributor.authorLópez Mejías, Raqueles_ES
dc.contributor.authorGenre, Fernandaes_ES
dc.contributor.authorGarcía-Bermúdez, Mercedeses_ES
dc.contributor.authorCorrales Martínez, Alfonsoes_ES
dc.contributor.authorGonzález-Juanatey, Carloses_ES
dc.contributor.authorLlorca Díaz, Francisco Javier es_ES
dc.contributor.authorMiranda-Filloy, José A.es_ES
dc.contributor.authorRueda Gotor, Javieres_ES
dc.contributor.authorBlanco Alonso, Ricardo es_ES
dc.contributor.authorCastañeda, Santoses_ES
dc.contributor.authorMartín, Javieres_ES
dc.contributor.authorGonzález-Gay Mantecón, Miguel Ángel es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2023-06-16T14:18:22Z
dc.date.available2023-06-16T14:18:22Z
dc.date.issued2013es_ES
dc.identifier.issn1478-6354es_ES
dc.identifier.issn1478-6362es_ES
dc.identifier.urihttps://hdl.handle.net/10902/29334
dc.description.abstractIntroduction: Rheumatoid arthritis (RA) is a complex polygenic disease associated with chronic inflammation, accelerated atherosclerosis and increased cardiovascular (CV) mortality. A recent meta-analysis has described the ZC3HC1 rs11556924 polymorphism as one of the most important signals associated with coronary artery disease (CAD) in non-rheumatic Caucasian individuals. In this study we evaluated the potential association of this gene polymorphism with subclinical atherosclerosis assessed by the evaluation of carotid intima-media thickness (cIMT) in RA patients. Methods: This study included 502 RA patients from Northern Spain. The ZC3HC1 rs11556924 polymorphism was genotyped with TaqMan single-nucleotide polymorphism (SNP) genotyping assays (C__31283062_10) in a 7900HT real-time polymerase chain reaction (PCR) system. cIMT was also assessed in these patients by carotid ultrasonography (US) technology. Results: RA patients carrying the TT genotype had significantly higher cIMT values than those homozygous for the CC genotype (mean ± standard deviation (SD): 0.76 ± 0.18 mm and mean ± SD: 0.71 ± 0.16 mm respectively; P = 0.03) even after adjusting the results for sex, age at the time of US study, follow-up time and traditional CV risk factors (P = 0.04) evidencing that the effect conferred by ZC3HC1 rs11556924 polymorphism is independent of the traditional CV risk factors. Conclusion: Our results indicate that ZC3HC1 rs11556924 polymorphism is associated with subclinical atherosclerosis in RA.es_ES
dc.format.extent5 p.es_ES
dc.language.isoenges_ES
dc.publisherBioMed Centrales_ES
dc.rightsAttribution 4.0 International. © 2013 López-Mejías et al.; licensee BioMed Central Ltd.*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceArthritis Research and Therapy, 2013, 15, 152es_ES
dc.titleThe ZC3HC1 rs11556924 polymorphism is associated with increased carotid intima-media thickness in patients with rheumatoid arthritises_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1186/ar4335es_ES
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 International. © 2013 López-Mejías et al.; licensee BioMed Central Ltd.Excepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International. © 2013 López-Mejías et al.; licensee BioMed Central Ltd.