| Literature DB >> 19440814 |
Chieko Kyogoku1, Akio Morinobu, Kunihiro Nishimura, Daisuke Sugiyama, Hiroshi Hashimoto, Yoshiaki Tokano, Tsuneyo Mimori, Chikashi Terao, Fumihiko Matsuda, Takayoshi Kuno, Shunichi Kumagai.
Abstract
Tyrosine kinase 2 (TYK2) is a type I interferon (IFN) signaling pathway gene and was previously reported to be a risk factor for systemic lupus erythematosus (SLE) in Caucasian populations. In order to test for its genetic association with SLE in a Japanese population, TYK2 single nucleotide polymorphisms (SNPs), rs2304256, rs12720270 and rs280519, were genotyped. A case-control association study was performed in a total of 411 Japanese SLE patients and 467 healthy controls. Linkage disequilibrium (LD) among TYK2 SNPs was examined. According to the data from 94 healthy controls, non-synonymous rs2304256 resulting in Val --> Phe substitution was revealed to be in a LD with rs12720270 and rs280519. Therefore, we further genotyped rs2304256 as a tag SNP in the full sample sets. As a result, no differences in genotype distribution and allelic frequencies of rs2304256 were found between SLE patients and healthy controls. In conclusion, TYK2 is not a genetic risk factor for SLE in a Japanese population. Our result suggests that there is an ethnic difference in the susceptibility genes for SLE.Entities:
Mesh:
Substances:
Year: 2009 PMID: 19440814 DOI: 10.1007/s10165-009-0173-1
Source DB: PubMed Journal: Mod Rheumatol ISSN: 1439-7595 Impact factor: 3.023