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Gene polymorphisms of interleukin-4, interleukin-10 and transforming growth factor-beta in Graves' disease.

机译:Graves病中白细胞介素4,白细胞介素10和转化生长因子β的基因多态性。

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Among genetic factors that may contribute to the development and progression of Graves' disease (GD) and its complications are polymorphisms in the genes encoding cytokines. The association between GD and the following polymorphisms in anti-inflammatory cytokines was studied in 107 patients with GD and 140 healthy controls: IL-4 (-1098T/G, -590T/C, -33C/T), IL-10 (-1082A/G, -819C/T, -592C/A) and TGF-beta (+869T/C, +915G/C). The following alleles and genotypes were significantly (P < 0.01 after correction for multiple testing) more frequent among patients: the IL-4 -1098G allele and GG genotype (OR = 3.12 and 105.00, respectively), IL-4 -33T allele and TT genotype (OR = 2.52 and 118.83, respectively), IL-10 -1082G allele and GG genotype (OR = 2.16 and 6.40, respectively), IL-10 -819T allele, TC and TT genotype (OR = 2.60, 3.68 and 6.76, respectively), IL-10 -592A allele, AC and AA genotype (OR = 2.41, 2.89 and 5.68, respectively), TGF-beta +869C allele and CC genotype (OR = 2.24 and 6.21, respectively), and TGF-beta +915C allele, CG and CC genotype (OR = 7.81, 11.80 and 20.40, respectively). The only allele and genotype with a lower frequency in patients were IL-4 -590T allele and TC genotype (OR = 0.47 and 0.08, respectively; P < 0.01). In conclusion, this study highlighted the importance of anti-inflammatory cytokine gene polymorphisms in susceptibility to GD.
机译:在可能导致Graves病(GD)及其并发症发生和发展的遗传因素中,编码细胞因子的基因具有多态性。在107例GD患者和140例健康对照中研究了GD与以下抗炎细胞因子多态性之间的关联:IL-4(-1098T / G,-590T / C,-33C / T),IL-10(- 1082A / G,-819C / T,-592C / A和TGF-beta(+ 869T / C,+ 915G / C)。下列等位基因和基因型在患者中显着更频繁(校正后为P <0.01)在患者中更为频繁:IL-4 -1098G等位基因和GG基因型(分别为OR = 3.12和105.00),IL-4 -33T等位基因和TT基因型(分别为OR = 2.52和118.83),IL-10 -1082G等位基因和GG基因型(分别为OR = 2.16和6.40),IL-10 -819T等位基因,TC和TT基因型(OR = 2.60、3.68和6.76, ),IL-10 -592A等位基因,AC和AA基因型(分别为OR = 2.41、2.89和5.68),TGF-beta + 869C等位基因和CC基因型(分别为OR = 2.24和6.21)和TGF-beta + 915C等位基因,CG和CC基因型(分别为OR = 7.81、11.80和20.40)。患者中仅有的频率较低的等位基因和基因型是IL-4 -590T等位基因和TC基因型(OR分别为0.47和0.08; P <0.01)。总之,本研究强调了抗炎细胞因子基因多态性在GD易感性中的重要性。

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