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Identification of LEF1 as a Susceptibility Locus for Kawasaki Disease in Patients Younger than 6 Months of Age

Authors
김혜지윤신원유정진윤경림이경일길홍량김기범한명기송민섭이형두하기수손세정Ryota EbataHiromichi HamadaHiroyuki SuzukiYoichiro KamataniMichiaki KuboKaoru ItoYoshihiro Onouchi홍영미장기영이종극
Issue Date
Jun-2018
Publisher
한국유전체학회
Keywords
genome-wide association study; Kawasaki disease; lymphoid enhancer binding factor1 (LEF1); single nucleotide polymorphism
Citation
Genomics & Informatics, v.16, no.2, pp 36 - 41
Pages
6
Journal Title
Genomics & Informatics
Volume
16
Number
2
Start Page
36
End Page
41
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/18924
DOI
10.5808/GI.2018.16.2.36
ISSN
1598-866X
2234-0742
Abstract
Kawasaki disease (KD) is an acute febrile vasculitis predominately affecting infants and children. The dominant incidence age of KD is from 6 months to 5 years of age, and the incidence is unusual in those younger than 6 months and older than 5 years of age. We tried to identify genetic variants specifically associated with KD in patients younger than 6 months or older than 5 years of age. We performed an age-stratified genome-wide association study using the Illumina HumanOmni1-Quad BeadChip data (296 cases vs. 1,000 controls) and a replication study (1,360 cases vs. 3,553 controls) in the Korean population. Among 26 candidate single nucleotide polymorphisms (SNPs) tested in replication study, only a rare nonsynonymous SNP (rs4365796: c.1106C>T, p.Thr369Met) in the lymphoid enhancer binding factor 1 (LEF1) gene was very significantly associated with KD in patients younger than 6 months of age (odds ratio [OR], 3.07; pcombined = 1.10 × 10-5), whereas no association of the same SNP was observed in any other age group of KD patients. The same SNP (rs4365796) in the LEF1 gene showed the same direction of risk effect in Japanese KD patients younger than 6 months of age, although the effect was not statistically significant (OR, 1.42; p = 0.397). This result indicates that the LEF1 gene may play an important role as a susceptibility gene specifically affecting KD patients younger than 6 months of age.
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