Mostrar el registro sencillo del ítem

dc.contributor.author
Maiti, Amit K.  
dc.contributor.author
Kim Howard, Xana  
dc.contributor.author
Viswanathan, Parvathi  
dc.contributor.author
Guillen, Laura Cristina  
dc.contributor.author
Rojas Villarraga, Adriana  
dc.contributor.author
Deshmukh, Harshal  
dc.contributor.author
Direskeneli, Haner  
dc.contributor.author
Saruhan Direskeneli, Güher  
dc.contributor.author
Cañas, Carlos  
dc.contributor.author
Tobón, Gabriel J.  
dc.contributor.author
Sawalha, Amr H.  
dc.contributor.author
Cherñavsky, Alejandra Claudia  
dc.contributor.author
Anaya, Juan Manuel  
dc.contributor.author
Nath, Swapan K.  
dc.date.available
2019-01-08T19:07:04Z  
dc.date.issued
2010-02  
dc.identifier.citation
Maiti, Amit K.; Kim Howard, Xana; Viswanathan, Parvathi; Guillen, Laura Cristina; Rojas Villarraga, Adriana; et al.; Confirmation of an association between rs6822844 at the IL2-IL21 region and multiple autoimmune diseases: Evidence of a general susceptibility locus; Wiley-liss, Div John Wiley & Sons Inc; Arthritis And Rheumatism; 62; 2; 2-2010; 323-329  
dc.identifier.issn
0004-3591  
dc.identifier.uri
http://hdl.handle.net/11336/67678  
dc.description.abstract
Objective. Autoimmune diseases often have susceptibility genes in common, indicating similar molecular mechanisms. Increasing evidence suggests that rs6822844 at the IL2-IL21 region is strongly associated with multiple autoimmune diseases in individuals of European descent. This study was undertaken to attempt to replicate the association between rs6822844 and 6 different immune-mediated diseases in non-European populations, and to perform disease-specific and overall meta-analyses using data from previously published studies. Methods. We evaluated case-control associations between rs6822844 and celiac disease (CD) in subjects from Argentina; rheumatoid arthritis (RA), type 1 diabetes mellitus (DM), primary Sjögren's syndrome (SS), and systemic lupus erythematosus (SLE) in subjects from Colombia; and Behçet's disease (BD) in subjects from Turkey. Allele and gene distributions were compared between cases and controls. Meta-analyses were performed using data from the present study and previous studies. Results. We detected significant associations of rs6822844 with SLE (P = 0.008), type 1 DM(P = 0.014), RA (P = 0.019), and primary SS (P = 0.033) but not with BD (P = 0.34) or CD (P = 0.98). We identified little evidence of population differentiation (FST = 0.01) within cases and controls from Argentina and Colombia, suggesting that association was not influenced by population substructure. Disease-specific meta-analysis indicated significant association for RA (Pmeta = 3.61 × 10-6), inflammatory bowel disease (IBD; Crohn's disease and ulcerative colitis) (Pmeta = 3.48 × 10-12), type 1 DM (Pmeta = 5.33 × 10-5), and CD (Pmeta = 5.30 × 10-3). Overall meta-analysis across all autoimmune diseases reinforced association with rs6822844 (23 data sets; Pmeta = 2.61 × 10-25, odds ratio 0.73 [95% confidence interval 0.69-0.78]). Conclusion. Our results indicate that there is an association between rs6822844 and multiple autoimmune diseases in non-European populations. Metaanalysis results strongly reinforce this robust association across multiple autoimmune diseases in both European-derived and non-European populations.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Wiley-liss, Div John Wiley & Sons Inc  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Rs6822844  
dc.subject
Il2-Il21 Region  
dc.subject
Autoimmune Diseases  
dc.subject.classification
Otras Medicina Básica  
dc.subject.classification
Medicina Básica  
dc.subject.classification
CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Confirmation of an association between rs6822844 at the IL2-IL21 region and multiple autoimmune diseases: Evidence of a general susceptibility locus  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2019-01-07T13:33:55Z  
dc.journal.volume
62  
dc.journal.number
2  
dc.journal.pagination
323-329  
dc.journal.pais
Estados Unidos  
dc.description.fil
Fil: Maiti, Amit K.. Oklahoma Medical Research Foundation; Estados Unidos  
dc.description.fil
Fil: Kim Howard, Xana. Oklahoma Medical Research Foundation; Estados Unidos  
dc.description.fil
Fil: Viswanathan, Parvathi. Oklahoma Medical Research Foundation; Estados Unidos  
dc.description.fil
Fil: Guillen, Laura Cristina. Universidad de Buenos Aires. Facultad de Medicina. Hospital de Clínicas General San Martín; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Rojas Villarraga, Adriana. Universidad del Rosario; Colombia  
dc.description.fil
Fil: Deshmukh, Harshal. Oklahoma Medical Research Foundation; Estados Unidos  
dc.description.fil
Fil: Direskeneli, Haner. Marmara University; Turquía  
dc.description.fil
Fil: Saruhan Direskeneli, Güher. Istanbul University; Turquía  
dc.description.fil
Fil: Cañas, Carlos. Fundación Valle del Lili; Colombia  
dc.description.fil
Fil: Tobón, Gabriel J.. Fundación Valle del Lili; Colombia  
dc.description.fil
Fil: Sawalha, Amr H.. University of Oklahoma; Estados Unidos  
dc.description.fil
Fil: Cherñavsky, Alejandra Claudia. Universidad de Buenos Aires. Facultad de Medicina. Hospital de Clínicas General San Martín; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Anaya, Juan Manuel. Oklahoma Medical Research Foundation; Estados Unidos  
dc.description.fil
Fil: Nath, Swapan K.. Oklahoma Medical Research Foundation; Estados Unidos  
dc.journal.title
Arthritis And Rheumatism  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/art.27222  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/full/10.1002/art.27222  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3028384/