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dc.contributor.authorNath, Swapan K.
dc.contributor.authorSawalha, Amr H.
dc.contributor.authorChernavsky, Alejandra C.
dc.contributor.authorAnaya, Juan-Manuel
dc.contributor.authorSaruhan-Direskeneli, Güher
dc.contributor.authorMaiti, Amit K.
dc.contributor.authorKim-Howard, Xana
dc.contributor.authorViswanathan, Parvathi
dc.contributor.authorGuillen, Laura
dc.contributor.authorRojas-Villarraga, Adriana
dc.contributor.authorDeshmukh, Harshal
dc.contributor.authorDireskeneli, Haner
dc.contributor.authorCanas, Carlos
dc.contributor.authorTobon, Gabriel J.
dc.date.accessioned2021-03-05T10:59:12Z
dc.date.available2021-03-05T10:59:12Z
dc.date.issued2010
dc.identifier.citationMaiti A. K. , Kim-Howard X., Viswanathan P., Guillen L., Rojas-Villarraga A., Deshmukh H., Direskeneli H., Saruhan-Direskeneli G., Canas C., Tobon G. J. , et al., "Confirmation of an association between rs6822844 at the IL2-IL21 region and multiple autoimmune diseases: Evidence of a general susceptibility locus", Arthritis and Rheumatism, cilt.62, ss.323-329, 2010
dc.identifier.issn0004-3591
dc.identifier.othervv_1032021
dc.identifier.otherav_a5e61396-140b-4e17-8003-d2d9204f609c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/110952
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=75749113734&origin=inward
dc.identifier.urihttps://doi.org/10.1002/art.27222
dc.description.abstractObjective. 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. © 2010, American College of Rheumatology.
dc.language.isoeng
dc.subjectROMATOLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectİmmünoloji ve Romatoloji
dc.titleConfirmation of an association between rs6822844 at the IL2-IL21 region and multiple autoimmune diseases: Evidence of a general susceptibility locus
dc.typeMakale
dc.relation.journalArthritis and Rheumatism
dc.contributor.department, ,
dc.identifier.volume62
dc.identifier.issue2
dc.identifier.startpage323
dc.identifier.endpage329
dc.contributor.firstauthorID195164


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