[No authors listed]
OBJECTIVE:The aim of this study was to determine whether phox homology domain containing serine/threonine kinase (PXK) and tyrosine kinase 2 (TYK2) confer susceptibility to systemic lupus erythematosus (SLE). MATERIALS AND METHODS:The authors conducted meta-analyses on associations between SLE susceptibility and the rs6445975 polymorphism of PXK and the rs2304256, rs12720270, rs280519, and rs1272036 polymorphisms of TYK2. RESULTS:A total of 13 separate comparisons studies were included in this meta-analysis. Meta-analysis identified an association between SLE and the 2 allele of the rs6445975 polymorphism in the overall population [odds ratio (OR)Â =Â 1.151, 95Â % confidence interval (CI)Â =Â 1.086-1.291, PÂ =Â 1.8E-06]. Stratification by ethnicity identified a significant association between this polymorphism and SLE in Europeans (ORÂ =Â 1.198, 95Â % CIÂ =Â 1.118-1.285, PÂ =Â 3.4E-07), but not in Asians. Meta-analysis identified a significant negative association between SLE and the 2 allele of the rs2304256 polymorphism in the overall population (ORÂ =Â 0.808, 95Â % CIÂ =Â 0.659-0.990, PÂ =Â 0.040), and a significant negative association was found in Europeans, but not in Asians. CONCLUSIONS:This meta-analysis shows that the rs6445975 polymorphism of PXK and the rs2304256 polymorphism of TYK2 are associated with the development of SLE in Europeans.
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