Lemire Mathieu
Ontario Institute for Cancer Research, 101 College Street, Suite 800, MaRS Centre, South Tower, Toronto, ON M5G0A3 Canada.
BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S33. doi: 10.1186/1753-6561-3-s7-s33.
Using single-nucleotide polymorphisms (SNPs), we sought to predict classical class I and class II human leukocyte antigen (HLA) alleles, and test for their associations with rheumatoid arthritis (RA) in the North American Rheumatoid Arthritis Consortium sample of cases and controls, genotyped on the Illumina HumanHap550 BeadChip. We use publicly available databases of SNP data and HLA data to find SNPs or SNP-haplotypes to be used as surrogates for each HLA allele. To reduce the confounding effects of linkage disequilibrium with the HLA-DRB1 locus, we tested for the association conditional on the presence or absence of a shared epitope allele on the same haplotype as the target HLA allele. Using SNP surrogates, we find that components of the DQ8 serotype (DQA10301:DQB10302) are associated with RA, irrespective of the presence or absence of a shared epitope allele on their respective haplotypes. Knowledge of the haplotype structure in the HLA region is still necessary for better interpretation of the results.
利用单核苷酸多态性(SNP),我们试图预测经典的I类和II类人类白细胞抗原(HLA)等位基因,并在北美类风湿关节炎联盟的病例和对照样本中检测它们与类风湿关节炎(RA)的关联,这些样本在Illumina HumanHap550 BeadChip上进行了基因分型。我们使用公开可用的SNP数据和HLA数据数据库来寻找用作每个HLA等位基因替代物的SNP或单倍型。为了减少与HLA-DRB1基因座连锁不平衡的混杂效应,我们在与目标HLA等位基因相同单倍型上存在或不存在共享表位等位基因的条件下测试了关联性。使用SNP替代物,我们发现DQ8血清型(DQA10301:DQB10302)的组成部分与RA相关,无论其各自单倍型上是否存在共享表位等位基因。为了更好地解释结果,了解HLA区域的单倍型结构仍然是必要的。