已发表论文

miRNA-137  基因中的 rs1625579 T>G 多态性使中国南方人群面临早发性川崎病的风险

 

Authors Che D, Li J, Fu L, Pi L, Rong X, Wang Y, Xu Y, Huang P, Chu M, Gu X

Received 14 May 2018

Accepted for publication 13 June 2018

Published 3 August 2018 Volume 2018:11 Pages 1055—1060

DOI https://doi.org/10.2147/IDR.S174140

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Andrew Yee

Peer reviewer comments 2

Editor who approved publication: Professor Suresh Antony

Background: Kawasaki disease (KD) mainly manifests as excessive inflammation and vascular endothelial cell injury. This disease generally occurs in children younger than 5 years of age and is more severe in children younger than 12 months. KD affects males and females at a ratio of 1.5:1. Polymorphisms of the rs1625579 locus in the miR-137  gene are associated with schizophrenia susceptibility, and high glucose-induced upregulation of miR-137  in vascular endothelial cells promotes monocyte chemotaxis and inflammatory cytokine secretion in gestational diabetes mellitus. However, researchers have not reported whether rs1625579 is associated with KD susceptibility or onset. Therefore, we investigated the relationship between the miRNA-137  rs1625579 T>G polymorphism and KD susceptibility. 
Methods: TaqMan real-time polymerase chain reaction was applied to determine the genotypes of 532 patients with KD (365 males and 167 females) and 623 control subjects (402 males and 221 females). 
Results: Comparison of all cases with all controls revealed that the rs1625579 T>G polymorphism was not associated with KD susceptibility. However, a subgroup analysis revealed that subjects with the rs1625579 TG/GG genotypes exhibited a significantly higher onset risk for KD before 12 months of age than carriers of the TT genotype (adjusted age and gender odds ratio=1.99, 95% CI=1.04–3.83; =0.039). 
Conclusion: Our results indicate that the rs1625579 T>G polymorphism confers a risk of early-onset KD in southern Chinese children.
Keywords: Kawasaki disease, miRNA-137, rs1625579, susceptibility, early onset



Table 3 Subgroup analyses of the relationship between the rs1625579 T>G polymorphism and KD susceptibility