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Abstract
Background: Recent studies have suggested that interleukin (IL)-18 gene (−137G/C) polymorphism is associated with rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE). However, other studies did not confirm this correlation. Objective: The objective of this study was to evaluate the relationships of IL-18 −137G/C and RA and SLE using a meta-analysis. Methods: Pubmed, Embase and Cochrane library databases were systemically searched. Data were extracted by two independent reviewers and pooled odds ratio (OR) with 95% confidence interval (CI) was calculated. Results: In RA, the overall ORs and 95% CIs of −137C were 1.03, 0.88–1.22 (p = 0.391); 1.22, 0.89–1.68 (p = 0.020) and 1.06, 0.93–1.21 (p = 0.110) in dominant, recessive, and additive models, respectively. Furthermore, in SLE, the overall ORs and 95% CIs of −137C were 1.10, 0.94–1.29 (p = 0.980); 1.21, 0.91–1.60 (p = 0.010) and 1.10, 0.97–1.24 (p = 0.454) in dominant, recessive, and additive models, respectively. IL-18 −137G/C could increase the risk of RA and SLE. No publication bias was found in this meta-analysis. After population stratification analysis, under recessive model, the pooled ORs and 95% CIs of −137C were 1.14, 0.82–1.60 (p = 0.008) and 1.01, 0.66–1.55 (p = 0.004) in European RA patients and Asian SLE patients, respectively. Conclusions: This meta-analysis showed that IL-18 −137G/C was a risk factor for RA and SLE, especially for RA in Europeans and SLE in Asians.
Notice of Cor
Changes have beenmade to this article since its original online publication date of 5 August, 2013.