| Literature DB >> 29017771 |
Rong Wang1, Yu-Lan Lu1, Hua-Tuo Huang1, Hai-Mei Qin1, Yan Lan2, Jun-Li Wang3, Chun-Fang Wang3, Ye-Sheng Wei4.
Abstract
Interleukin (IL) 13 plays a critical role in inflammatory diseases, including systemic lupus erythematosus (SLE). This study aims to explore the potential association of IL-13 polymorphisms with the risk of SLE. We genotyped IL-13 rs20541, rs848 and rs1295686 using Snapshot SNP genotyping assays. Plasma IL-13 level was determined by enzyme-linked immunosorbent assay (ELISA). We found that rs20541 was associated with increased risk of SLE (CT vs. CC: adjusted OR=1.43, 95%CI, 1.04-1.99, P=.030; TT vs. CC: adjusted OR=1.73, 95%CI, 1.10-2.73, P=.018; CT/TT vs. CC: adjusted OR=1.50, 95%CI, 1.10-2.04, P=.010; T vs. C adjusted OR=1.34, 95%CI, 1.08-1.93, P=.031). CT and TT genotypes in rs20541 were associated with increased risk of renal disorder in SLE (CT vs. CC: adjusted OR=1.97, 95%CI, 1.18-3.28, P=.009; TT vs. CC: adjusted OR=2.42, 95%CI, 1.22-4.77, P=.011). Moreover, The concentration of IL-13 was significantly elevated in rs20541 CT/TT genotypes compared with CC genotype (P<.001). These results suggest that rs20541 CT/TT genotypes may be a risk factor for SLE, probably by increasing the level of IL-13.Entities:
Keywords: Gene; IL-13; Inflammation; Polymorphism; Systemic lupus erythematosus
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Year: 2017 PMID: 29017771 DOI: 10.1016/j.cyto.2017.09.034
Source DB: PubMed Journal: Cytokine ISSN: 1043-4666 Impact factor: 3.861