HLA-B*58:01 and rs9263726 have a linkage, but not absolute linkage disequilibrium in Han Chinese population

Drug Metab Pharmacokinet. 2018 Oct;33(5):228-231. doi: 10.1016/j.dmpk.2018.08.001. Epub 2018 Aug 14.

Abstract

HLA-B*58:01 has been demonstrated to be associated with allopurinol-induced severe cutaneous adverse reactions. Since HLA-B*58:01 is too complicated to be identified, it is necessary to select an appropriate surrogate biomarker. In Japan, the rs9263726 allele was considered as a surrogate biomarker for HLA-B*58:01, but this was not the case with the Australian cohort. Due to the conflict results, in this study, we aim to demonstrate whether the rs9263726 allele is a surrogate biomarker for HLA-B*58:01 in Han Chinese population. A total of 353 samples (200 cases from the south and 153 cases from the north) were selected to detect HLA-B*58:01 and rs9263726 allele. The HLA-B*58:01 was identified by sequencing-based method, and the rs9263726 allele was identified by Taqman SNP Genotyping Assays. The results showed that the two alleles had a linkage, but not absolute linkage disequilibrium in Han Chinese population.

Keywords: Allopurinol-induced SCARs; HLA-B*58:01; Han Chinese; Linkage disequilibrium; rs9263726.

MeSH terms

  • Alleles*
  • China
  • Ethnicity / genetics*
  • Genotype
  • HLA-B Antigens / genetics*
  • Humans
  • Linkage Disequilibrium*

Substances

  • HLA-B Antigens