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Confirmation of an association between rs6822844 at the Il2–Il21 region and multiple autoimmune diseases: Evidence of a general susceptibility locus
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...
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Published in: | Arthritis and rheumatism 2010-02, Vol.62 (2), p.323-329 |
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Main Authors: | , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 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. Meta‐analysis results strongly reinforce this robust association across multiple autoimmune diseases in both European‐derived and non‐European populations. |
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ISSN: | 0004-3591 1529-0131 |
DOI: | 10.1002/art.27222 |