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Confirmation of an association between rs6822844 at theIl2-Il21region and multiple autoimmune diseases: Evidence of a general susceptibility locus

Authors :
Amr H. Sawalha
Adriana Rojas-Villarraga
Juan-Manuel Anaya
Harshal Deshmukh
Amit K. Maiti
Laura Guillén
Gabriel J. Tobón
Haner Direskeneli
Xana Kim-Howard
Carlos A. Cañas
Swapan K. Nath
Alejandra C. Cherñavsky
Güher Saruhan-Direskeneli
Parvathi Viswanathan
Source :
CONICET Digital (CONICET), Consejo Nacional de Investigaciones Científicas y Técnicas, instacron:CONICET, Repositorio EdocUR-U. Rosario, Universidad del Rosario, instacron:Universidad del Rosario
Publication Year :
2010
Publisher :
Wiley, 2010.

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. Fil: Maiti, Amit K.. Oklahoma Medical Research Foundation; Estados Unidos Fil: Kim Howard, Xana. Oklahoma Medical Research Foundation; Estados Unidos Fil: Viswanathan, Parvathi. Oklahoma Medical Research Foundation; Estados Unidos 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 Fil: Rojas Villarraga, Adriana. Universidad del Rosario; Colombia Fil: Deshmukh, Harshal. Oklahoma Medical Research Foundation; Estados Unidos Fil: Direskeneli, Haner. Marmara University; Turquía Fil: Saruhan Direskeneli, Güher. Istanbul University; Turquía Fil: Cañas, Carlos. Fundación Valle del Lili; Colombia Fil: Tobón, Gabriel J.. Fundación Valle del Lili; Colombia Fil: Sawalha, Amr H.. University of Oklahoma; Estados Unidos 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 Fil: Anaya, Juan Manuel. Oklahoma Medical Research Foundation; Estados Unidos Fil: Nath, Swapan K.. Oklahoma Medical Research Foundation; Estados Unidos

Details

ISSN :
15290131 and 00043591
Volume :
62
Database :
OpenAIRE
Journal :
Arthritis & Rheumatism
Accession number :
edsair.doi.dedup.....3b2570665e24981c591b91b59c0580dd
Full Text :
https://doi.org/10.1002/art.27222