| Literature DB >> 30971808 |
Jae-Jung Kim1, Sin Weon Yun2, Jeong Jin Yu3, Kyung Lim Yoon4, Kyung-Yil Lee5, Hong-Ryang Kil6, Gi Beom Kim7, Myung-Ki Han8, Min Seob Song9, Hyoung Doo Lee10, Kee Soo Ha11, Sejung Sohn12, Ryota Ebata13, Hiromichi Hamada14, Hiroyuki Suzuki15, Kaoru Ito16, Yoshihiro Onouchi16,17, Young Mi Hong12, Gi Young Jang11, Jong-Keuk Lee18.
Abstract
Kawasaki disease (KD) is a systemic vasculitis affecting infants and children; it manifests as fever and signs of mucocutaneous inflammation. Intravenous immunoglobulin (IVIG) treatment effectively attenuates the fever and systemic inflammation. However, 10-20% patients are unresponsive to IVIG. To identify genetic variants influencing IVIG non-response in KD, a genome-wide association study (GWAS) and a replication study were performed using a total of 148 IVIG non-responders and 845 IVIG-responders in a Korean population. rs28662 in the sterile alpha motif domain-containing protein 9-like (SAMD9L) locus showed the most significant result in the joint analysis of GWAS and replication samples (odds ratio (OR) = 3.47, P = 1.39 × 10-5). The same SNP in the SAMD9L locus was tested in the Japanese population, and it revealed a more significant association in a meta-analysis with Japanese data (OR = 4.30, P = 5.30 × 10-6). These results provide new insights into the mechanism of IVIG response in KD.Entities:
Mesh:
Substances:
Year: 2019 PMID: 30971808 DOI: 10.1038/s41397-019-0085-1
Source DB: PubMed Journal: Pharmacogenomics J ISSN: 1470-269X Impact factor: 3.550