TBXA2R rs4523 G allele is associated with decreased susceptibility to Kawasaki disease. (November 2018)

• Record Type: Journal Article
• Authors: Che, Di; Pi, Lei; Xu, Yufen; Fu, LanYan; Zhou, Huazhong; Wang, Zhouping; Huang, Ping; Zhang, Li; Gu, Xiaoqiong
• Is Part Of: Cytokine. Volume 111(2018)
• Page Start: 216
• Page End: 221
• Publication Date: 2018-11
• Subjects: Kawasaki disease -- TBXA2R -- Genetic susceptibility -- Polymorphism; Cytokines -- Periodicals; 571.844
• DOI: 10.1016/j.cyto.2018.08.029
• Languages: English
• ISSNs: 1043-4666

Abstract

Highlights: TBXA2R rs4523 G variant genotypes was significantly decrease risk of Kawasaki disease. rs4523 AG/GG variant genotypes protective effect was more predominant for children 12–60 months of age and females then the AA genotype. rs4523 G allele may influence plasma levels of 11-DH-TXB2 in Kawasaki disease patient. Abstract: Kawasaki disease is a multi-system vasculitis and a primary cause of acquired heart disease among children. Genetic factors may increase susceptibility to Kawasaki disease. TBXA2R is a G-protein-coupled receptor that participates in tissue inflammation and is associated with susceptibility to several diseases, but its relevance in Kawasaki disease is unclear. We genotyped TBXA2R (rs1131882 and rs4523) in 694 Kawasaki disease cases and 657 healthy controls. Odds ratios (ORs) and 95% confidence intervals (CIs) were used to evaluate the intensity of the associations. We found a significantly decreased risk of Kawasaki disease associated with TBXA2R rs4523 G variant genotypes (AG vs AA: adjusted OR = 0.788, 95%CI = 0.626–0.993; GG vs AA: adjusted OR = 0.459, 95%CI = 0.258–0.815; AG/GG vs AA: adjusted OR = 0.744, 95%CI = 0.595–0.929; GG vs AG/AA: adjusted OR = 0.497, 95% CI = 0.281–0.879). In the combined analysis of the two single-nucleotide polymorphisms (SNPs), we found that individuals with two unfavorable genotypes exhibited decreased risk for Kawasaki disease (adjusted OR = 0.754, 95%CI = 0.577–0.985) compared with those who did not have or one unfavorable genotypes. This cumulative effect on protection is effect-genotype dose-dependent (ptrend = 0.022). Moreover, the combined analysis indicated that the two unfavorable genotypes were associated with a decreased risk of Kawasaki disease in children 12–60 months of age, females and the subgroup with non-coronary artery lesion (NCAL) formation compared with those who did not have or one unfavorable genotypes. In conclusion, the TBXA2R rs4523 G allele may contribute to protection against Kawasaki disease and decreased risk of coronary artery aneurysm complications in a southern Chinese population.