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Gene-gene and gene-sex epistatic interactions of DNMT1, DNMT3A and DNMT3B in autoimmune thyroid disease

机译:DNMT1,DNMT3A和DNMT3B在自身免疫性甲状腺疾病中的基因-基因和基因-性别上位相互作用

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References(42) The aim of this study was to investigate the associations of DNA methyltransferases (DNMTs) polymorphisms with susceptibility to autoimmune thyroid diseases (AITDs) and to test gene-gene/gene-sex epistasis interactions. Eight single-nucleotide polymorphisms (SNPs) in DNMT1, DNMT3A and DNMT3B were selected and genotyped by multiplex polymerase chain reaction combined with ligase detection reaction method (PCR-LDR). A total of 685 Graves’ disease (GD) patients, 353 Hashimoto’s thyroiditis (HT) patients and 909 healthy controls were included in the final analysis. Epistasis was tested by additive model, multiplicative model and general multifactor dimensionality reduction (general MDR). Rs2424913 (DNMT3B) and rs2228611 (DNMT1) were associated with susceptibility to AITD and GD in the dominant and overdominant model, respectively (rs2424913: P=0.009 for AITD, P=0.0041 for GD; rs2228611: P=0.035 for AITD, P=0.043 for GD). Multiplicative and multiple high dimensional gene-gene or gene-sex interactions were also observed in this study. We have found evidence for a potential role of rs2424913 (DNMT3B) and rs2228611 (DNMT1) in AITD susceptibility and identified novel gene-gene/gene-sex interactions in AITD. Our study may highlight sex and genes of DNMTs family as contributors to the pathogenesis of AITD.
机译:参考文献(42)这项研究的目的是研究DNA甲基转移酶(DNMT)多态性与自身免疫性甲状腺疾病(AITD)的易感性之间的关系,并测试基因-基因/基因-性别上位性相互作用。通过多重聚合酶链反应结合连接酶检测反应方法(PCR-LDR),选择了DNMT1,DNMT3A和DNMT3B中的八个单核苷酸多态性(SNP),并进行了基因分型。最终分析共包括685名Graves病(GD)患者,353名Hashimoto甲状腺炎(HT)患者和909名健康对照。通过加性模型,乘法模型和一般多因素降维(通用MDR)测试上位性。 Rs2424913(DNMT3B)和rs2228611(DNMT1)在显性和显性模型中分别与对AITD和GD的敏感性相关(rs2424913:AITD的P = 0.009,GD的P = 0.0041; rs2228611:AITD的P = 0.035,P = GD为0.043)。在这项研究中还观察到了多维和多维的基因-基因或基因-性别相互作用。我们已经发现rs2424913(DNMT3B)和rs2228611(DNMT1)在AITD易感性中的潜在作用的证据,并确定了AITD中新型的基因-基因/基因-性相互作用。我们的研究可能会强调DNMTs家族的性别和基因,这是AITD发病机理的原因。

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