Registro completo |
Provedor de dados: |
Genet. Mol. Biol.
|
País: |
Brazil
|
Título: |
Clinical evaluation of a substitute of HLA-B*58:01 in different Chinese ethnic groups
|
Autores: |
Zhang,Xinju
Jin,Lei
Wu,Zhiyuan
Ma,Weizhe
Chen,Yuming
Chen,Gang
Wang,Lixin
Guan,Ming
|
Data: |
2018-09-01
|
Ano: |
2018
|
Palavras-chave: |
Rs9263726
HLA-B*58:01
Allopurinol hypersensitivity reaction
Tag SNP
|
Resumo: |
Abstract The goal of this research was to investigate the linkage disequilibrium between rs9263726 and HLA-B*58:01 in different Chinese ethnic groups (Han, Tibet, and Hui) and to study the feasibility of rs9263726 replacing HLA-B*58:01 as an efficient indicator of potential allopurinol hypersensitivity syndrome. In this study, rs9263726 and HLA-B*58:01 were detected in all samples. For samples of individuals whose rs9263726 genotypes were not consistent with HLA-B*58:01, we did high-resolution typing of HLA-B gene to further confirm the correlation of rs9263726 genotype and special HLA-B alleles. We confirmed that the linkage disequilibrium between rs9263726 and HLA-B*58:01 was more significant in the Han ethnic group (r2=0.886, D’=1.0) than in the Tibet and Hui ethnic groups (for Tibetan, r2=0.606, D’=0.866; for Hui, r2=0.622, D’=0.924). For Han Chinese, samples with the GG genotype of rs9263726 did not carry HLA-B*58:01, while AA genotype samples were homozygous carriers of HLA-B*58:01. However, GA genotype samples of rs9263726 required a more sophisticated HLA-B genotyping assay before it was possible to identify whether they were HLA-B*58:01 carriers or not. For Tibetan and Hui, the linkage disequilibrium between rs9263726 and HLA-B*58:01 was not significant. Therefore, rs9263726 cannot replace HLA-B*58:01 in these two groups.
|
Tipo: |
Info:eu-repo/semantics/article
|
Idioma: |
Inglês
|
Identificador: |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572018000400578
|
Editor: |
Sociedade Brasileira de Genética
|
Relação: |
10.1590/1678-4685-gmb-2017-0258
|
Formato: |
text/html
|
Fonte: |
Genetics and Molecular Biology v.41 n.3 2018
|
Direitos: |
info:eu-repo/semantics/openAccess
|
|