Why the study?
Coronary artery lesions are the most disastrous complication of Kawasaki disease, but the relationship between the lncRNA rs1814343 polymorphism and Kawasaki disease risk remains elusive.
Is the lncRNA rs1814343 C > T polymorphism associated with the risk of coronary artery lesions in Kawasaki disease patients?
Is the lncRNA rs1814343 C > T polymorphism associated with the risk of coronary artery lesions in Kawasaki disease patients?
The TT variant of the lncRNA rs1814343 polymorphism is associated with an increased risk of coronary artery lesions in southern Chinese children with Kawasaki disease.
rs1814343 TT genotype was associated with higher CAL risk in KD; leaves open utility for risk stratification pending validation.
BACKGROUND: Kawasaki disease (KD) is a multisystemic angiitis, and its most disastrous complication is coronary artery lesions (CALs). Recently, the role of long non-coding RNAs (lncRNAs) in KD has been reported. rs1814343 is a lncRNA, but the relationship between the lncRNA rs1814343 polymorphism and KD risk remains elusive. METHODS: We enrolled 1625 Kawasaki disease patients (583 patients with CAL and 1042 without CAL) and 1000 healthy controls from a southern Chinese population. We genotyped the rs1814343 C > T polymorphism in KD and control patients using the TaqMan method. The odds ratio (OR) and 95% confidence interval (CI) were used to estimate the strength of the association. RESULTS: There was no significant association between the lncRNA rs1814343 C > T polymorphism and KD susceptibility. However, we stratified patients in this study by CAL and sex. First, compared with the control groups, we found that the rs1814343 genotype increased risk for KD patients with CAL (TT vs. CC + CT: OR = 1.36, 95% CI = 1.08-1.71, p = 0.009). Moreover, when KD patients were stratified by CAL, the TT genotypes of this lncRNA polymorphism contributed to a relatively higher occurrence of KD with CAL than that was found in the CC/CT genotype patients (TT vs. CC + CT: OR = 1.35, 95% CI = 1.07-1.69, p = 0.011). In addition, our research suggested that the TT variant genotype in the lncRNA rs1814343 had an obvious risk of KD with CAL susceptibility in male children. CONCLUSION: The lncRNA rs1814343 C > T polymorphism was related to higher susceptibility of KD with CAL.
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Chen et al. (2023) studied this question.
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