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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
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