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首页> 外文期刊>International journal of immunogenetics >Single-nucleotide polymorphisms of IRF8 gene are associated with systemic lupus erythematosus in Chinese Han population.
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Single-nucleotide polymorphisms of IRF8 gene are associated with systemic lupus erythematosus in Chinese Han population.

机译:IRF8基因的单核苷酸多态性与中国汉族人群系统性红斑狼疮有关。

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Interferon regulatory factor 8 (IRF8) has been shown to have diverse roles in the regulation of the immune system. Two recent studies had revealed the association between the single-nucleotide polymorphisms (SNPs; rs11644034 and rs2280381) of IRF8 and systemic lupus erythematosus (SLE) in a multiethnic population. The purpose of this study was to evaluate whether the association could be replicated in a Chinese Han population. Genotypes were determined by a multiplex polymerase chain reaction-ligase detection reaction (PCR-LDR) in 358 patients and 357 geographically matched healthy controls. Significant differences in genotype frequency were found between SLE and control individuals (rs11644034: AA vs. GG, P = 0.014, odds ratio (OR) = 0.980, 95% confidence internal (CI): 0.964-0.996; rs2280381: CC vs. TT, P = 0.005, OR = 0.150, 95% CI: 0.033-0.676). Conditional logistic regression analysis showed that the association of rs2280381 remained significant (P adjusted = 0.028) after adjustment for rs11644034, but not vice versa (P adjusted = 0.361).When stratifying patients with SLE according to clinical subtypes, SNP rs2280381 was found to be associated with low complement in patients with SLE. However, SNP rs11644034 was not found to be associated with SLE clinical subgroups. Analysis of the haplotypes revealed that haplotype G-T and G-C were also significantly associated with SLE (P = 0.002 and P = 0.012, respectively). Our study indicated that the IRF8 gene polymorphisms might be associated with susceptibility to SLE and with disease-related clinical manifestations in Chinese Han population.
机译:干扰素调节因子8(IRF8)已被证明在免疫系统的调节中具有多种作用。最近的两项研究揭示了IRF8的单核苷酸多态性(SNPs; rs11644034和rs2280381)与多种族人群的系统性红斑狼疮(SLE)之间的关联。这项研究的目的是评估该关联是否可以在中国汉族人群中复制。通过多重聚合酶链反应-连接酶检测反应(PCR-LDR)在358位患者和357位地理匹配的健康对照中确定基因型。在SLE和对照个体之间发现基因型频率的显着差异(rs11644034:AA vs. GG,P = 0.014,比值比(OR)= 0.980,95%置信度内部(CI):0.964-0.996; rs2280381:CC vs.TT ,P = 0.005,OR = 0.150,95%CI:0.033-0.676)。条件Logistic回归分析显示,对rs11644034进行调整后,rs2280381的关联仍显着(P调整= 0.028),反之则不(P调整= 0.361)。根据临床亚型对SLE患者进行分层时,发现SNP rs2280381是与SLE患者补体低相关。但是,未发现SNP rs11644034与SLE临床亚组相关。单倍型分析表明,单倍型G-T和G-C也与SLE显着相关(分别为P = 0.002和P = 0.012)。我们的研究表明,IRF8基因多态性可能与中国汉族人群对SLE的易感性以及疾病相关的临床表现有关。

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