Abstract

Genome-wide association studies (GWASs) have identified multiple single nucleotide polymorphisms (SNPs) associated with Kawasaki disease (KD). In this study, we replicated the associations of 10 GWAS-identified SNPs with KD in a Han Chinese population. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated by logistic regression, and cumulative effect of non-risk genotypes were also performed. Although none of the SNPs reached the corrected significance level, 4 SNPs showed nominal associations with KD risk. Compared with their respective wild type counterparts, rs1801274 AG+GG genotypes and rs3818298 TC+CC genotypes were nominally associated with the reduced risk of KD (OR = 0.77, 95% CI = 0.59–0.99, P = 0.045; OR = 0.74, 95% CI = 0.56–0.98, P = 0.038). Meanwhile, rs1801274 GG genotype, rs2736340 CC genotype or rs4813003 TT genotype showed a reduced risk trend (OR = 0.57, 95% CI = 0.35–0.93, P = 0.024; OR = 0.46, 95% CI = 0.26–0.83, P = 0.010; OR = 0.64, 95% CI = 0.43–0.94, P = 0.022), compared with rs1801274 AG+AA genotypes, rs2736340 CT+TT genotypes or rs4813003 TC+CC genotypes, respectively. Furthermore, a cumulative effect was observed with the ORs being gradually decreased with the increasing accumulative number of non-risk genotypes (Ptrend<0.001). In conclusion, our study suggests that 4 GWAS-identified SNPs, rs2736340, rs4813003, rs3818298 and rs1801274, were nominally associated with KD risk in a Han Chinese population individually and jointly.

Highlights

  • Genome-wide association studies (GWASs) have identified multiple single nucleotide polymorphisms (SNPs) associated with Kawasaki disease (KD)

  • None of the SNPs reached the corrected significance level, 4 SNPs showed nominal associations with KD risk. Compared with their respective wild type counterparts, rs1801274 AG1GG genotypes and rs3818298 TC1CC genotypes were nominally associated with the reduced risk of KD (OR50.77, 95% CI50.59–0.99, P50.045; OR50.74, 95% CI50.56–0.98, P50.038)

  • A total of 10 SNPs located in 3 novel loci (COPB2, ERAP1, IGHV) were found to be associated with KD in a Han Chinese population residing in Taiwan, which was the first KD GWAS conducted in this population[14]

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Summary

Introduction

Genome-wide association studies (GWASs) have identified multiple single nucleotide polymorphisms (SNPs) associated with Kawasaki disease (KD). A total of 10 SNPs located in 3 novel loci (COPB2, ERAP1, IGHV) were found to be associated with KD in a Han Chinese population residing in Taiwan, which was the first KD GWAS conducted in this population[14]. Another GWAS performed in Europeans and Asians identified that 2 loci (FCGR2A, MIA-RAB4B) contributed to KD risk[15]. We carried out a replication study on the association between GWAS-identified SNPs, alone and in accumulation with KD risk in another Han Chinese population in Southeast of China

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