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dc.contributor.authorTeruel, Maríaes_ES
dc.contributor.authorSimeón, Carmen P.es_ES
dc.contributor.authorBroen, Jasperes_ES
dc.contributor.authorVonk, Madelon C.es_ES
dc.contributor.authorCarreira, Patriciaes_ES
dc.contributor.authorCamps, María Teresaes_ES
dc.contributor.authorGarcía-Portales, Rosaes_ES
dc.contributor.authorDelgado-Frías, Esmeraldaes_ES
dc.contributor.authorGallego, Maríaes_ES
dc.contributor.authorEspinosa, Gerardes_ES
dc.contributor.authorBeretta, Lorenzoes_ES
dc.contributor.authorAiró, Paoloes_ES
dc.contributor.authorLunardi, Claudioes_ES
dc.contributor.authorRiemekasten, Gabrielaes_ES
dc.contributor.authorWitte, Torstenes_ES
dc.contributor.authorKrieg, Thomases_ES
dc.contributor.authorKreuter, Alexanderes_ES
dc.contributor.authorDistler, Jörg H. W.es_ES
dc.contributor.authorGonzález-Gay Mantecón, Miguel Ángel es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2024-01-30T14:26:00Z
dc.date.available2024-01-30T14:26:00Z
dc.date.issued2012es_ES
dc.identifier.issn1478-6354es_ES
dc.identifier.issn1478-6362es_ES
dc.identifier.otherSAF2009-11110es_ES
dc.identifier.urihttps://hdl.handle.net/10902/31324
dc.description.abstractIntroduction: The aim of the present study was to investigate the possible role of CD40 and CD40 ligand (CD40LG) genes in the susceptibility and phenotype expression of systemic sclerosis (SSc). Methods: In total, 2,670 SSc patients and 3,245 healthy individuals from four European populations (Spain, Germany, The Netherlands, and Italy) were included in the study. Five single-nucleotide polymorphisms (SNPs) of CD40 (rs1883832, rs4810485, rs1535045) and CD40LG (rs3092952, rs3092920) were genotyped by using a predesigned TaqMan allele-discrimination assay technology. Meta-analysis was assessed to determine whether an association exists between the genetic variants and SSc or its main clinical subtypes. Results: No evidence of association between CD40 and CD40LG genes variants and susceptibility to SSc was observed. Similarly, no significant statistical differences were observed when SSc patients were stratified by the clinical subtypes, the serologic features, and pulmonary fibrosis. Conclusions: Our results do not suggest an important role of CD40 and CD40LG gene polymorphisms in the susceptibility to or clinical expression of SSc.es_ES
dc.description.sponsorshipWe thank Sofia Vargas, Sonia Garcia, and Gema Robledo for their excellent technical assistance, and all the patients and healthy controls for kindly accepting their essential collaboration. We thank Banco Nacional de ADN (University of Salamanca, Spain) for supplying part of the control material. We also thank EUSTAR (The EULAR Scleroderma Trials and Research Group) and the German Network of Systemic Sclerosis for the facilitation of this project. This work was supported by the following grants. JM was funded by SAF2009-11110 from the Spanish Ministry of Science, by CTS-4977 and PI-0590-2010 from Junta de Andalucía, and by RETICS Program, RD08/0075 (RIER) from Instituto de Salud Carlos III (ISCIII), within the VI PN de I+D+i 2008-2011 (FEDER). T.R.D.J.R. was funded by the VIDI laureate from the Dutch Association of Research (NWO) and Dutch Arthritis Foundation (National Reumafonds). JM and TRDJR were sponsored by the Orphan Disease Program grant from the European League Against Rheumatism (EULAR). TW was awarded grants by DFG WI 1031/6.1 and DFG KFO 250 TP03. MT was supported by Spanish Ministry of Science through the program Juan de la Cierva (JCI-2010-08227). Spanish Scleroderma Group: Norberto Ortego-Centeno, José Luis Callejas, and Raquel Ríos, Systemic Autoimmune Diseases Unit, Department of Internal Medicine, Hospital Clínico Universitario San Cecilio, Granada; Nuria Navarrete and Antonio Garcia, Department of Internal Medicine, Hospital Virgen de las Nieves, Granada; Antonio Fernández-Nebro, Department of Rheumatology, Hospital Carlos Haya, Málaga; María F. González-Escribano, Department of Immunology, Hospital Virgen del Rocío, Sevilla; Julio Sánchez-Román and Mª Jesús Castillo, Department of Internal Medicine, Hospital Virgen del Rocío, Sevilla; Mª Ángeles Aguirre and Inmaculada Gómez-Gracia, Department of Rheumatology, Hospital Reina Sofía, Córdoba; Benjamín Fernández-Gutiérrez and Luis Rodríguez-Rodríguez, Department of Rheumatology, Hospital Clínico San Carlos, Madrid; Esther Vicente, Department of Rheumatology, Hospital La Princesa, Madrid; Mónica Fernández Castro and José Luis Andreu, Department of Rheumatology, Hospital Puerta del Hierro, Madrid; Paloma García de la Peña, Department of Rheumatology, Hospital Universitario Madrid Norte Sanchinarro, Madrid; Francisco Javier López-Longo and Lina Martínez-Estupiñán, Department of Rheumatology, Hospital General Universitario Gregorio Marañón, Madrid; Anna Pros, Department of Rheumatology, Hospital Del Mar, 08003 Barcelona; Vicente Fonollosa, Department of Internal Medicine, Hospital Valle de Hebrón, Barcelona; Carlos Tolosa, Department of Internal Medicine, Hospital Parc Tauli, Sabadell; Mónica Rodríguez Carballeira, Department of Internal Medicine, Hospital Universitari Mútua Terrasa, Barcelona; Ivan Castellví, Unidad de Reumatología, Department of Internal Medicine, Hospital de la Santa Creu i Sant Pau, Barcelona; Francisco Javier Narváez, Department of Rheumatology, Hospital Universitari de Bellvitge, Barcelona; Francisco Javier Blanco-García, Natividad Oreiro, and María Ángeles Robles, Department of Rheumatology, INIBIC-Hospital Universitario A Coruña, A Coruña; María Victoria Egurbide, Department of Internal Medicine, Hospital de Cruces, Vizcaya; Luis Sáez-Comet, Systemic Autoimmune Diseases Unit, Department of Internal Medicine, Hospital Universitario Miguel Servet, Zaragoza; Ricardo Blanco, Department of Rheumatology, Hospital Universitario Marqués de Valdecilla, Santander; Bernardino Díaz and Luis Trapiella, Department of Internal Medicine, Hospital Central de Asturias, Oviedo; Federico Díaz and Vanesa Hernández, Department of Rheumatology, Hospital Universitario de Canarias, Tenerife; Emma Beltrán, Department of Rheumatology, Hospital del Doctor Peset Aleixandre, Valencia; and José Andrés Román-Ivorra, Department of Rheumatology, Hospital Universitari i Politecnic La Fe, Valencia.
dc.format.extent6 p.es_ES
dc.language.isoenges_ES
dc.language.isofraes_ES
dc.publisherBioMed Centrales_ES
dc.rightsAttribution 4.0 International. © 2012 Teruel et al.; licensee BioMed Central Ltd.*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceArthritis Research & Therapy, 2012, 14(3), R154es_ES
dc.titleAnalysis of the association between CD40 and CD40 ligand polymorphisms and systemic sclerosises_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1186/ar3890es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1186/ar3890es_ES
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 International. © 2012 Teruel et al.; licensee BioMed Central Ltd.Excepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International. © 2012 Teruel et al.; licensee BioMed Central Ltd.