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Interleukin 18 (IL18) gene promoter polymorphisms are associated with type 1 diabetes mellitus in Brazilian patients

机译:白细胞介素18(IL18)基因启动子多态性与巴西患者的1型糖尿病相关

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摘要

Interleukin 18 (IL-18) is a cytokine that plays an important role in the Th1 response, by its ability to induce IFN-γ production in T cells and natural killer cells. Functional variants of IL18 gene has been reported as associated with type 1 diabetes (T1D). In the present study were analyzed three promoter single nucleotide polymorphisms (SNPs), at -656 (rs1946519), -607 (rs1946518) and -137 (rs187238) position, in 181 children and adolescents with T1D and 122 healthy individuals, both from metropolitan area of Recife, Northeast of Brazil. T1D patients were stratified according to the presence autoimmune thyroiditis and celiac disease. Allele and genotype frequencies of IL18 SNPs were Hardy-Weinberg equilibrium in patients and controls. The allele -137G and the haplotype -656G/-607C/-137G were more frequent in T1D patients (OR=1.82 and 1.97, respectively) then in healthy controls. However, those SNPs were not associated with the age of T1D onset as well as with the insurgence of AITD and/or CD in concomitant with T1D patients. Our findings suggest an association between IL18 promoter SNPs and susceptibility to T1D in Brazilian patients.
机译:白介素18(IL-18)是一种细胞因子,由于其在T细胞和自然杀伤细胞中诱导IFN-γ产生的能力而在Th1反应中起重要作用。已经报道IL18基因的功能变体与1型糖尿病(T1D)有关。在本研究中,分析了181名患有T1D的儿童和青少年以及122名健康个体的三个启动子单核苷酸多态性(SNP),分别位于-656(rs1946519),-607(rs1946518)和-137(rs187238)位置。巴西东北部累西腓地区。根据自身免疫性甲状腺炎和乳糜泻的存在,对T1D患者进行分层。 IL18 SNP的等位基因和基因型频率在患者和对照组中为Hardy-Weinberg平衡。与健康对照组相比,T1D患者中等位基因-137G和单倍型-656G / -607C / -137G更为常见(分别为OR = 1.82和1.97)。然而,这些SNPs与T1D发作的年龄以及伴随T1D患者的AITD和/或CD的暴发无关。我们的发现表明,巴西患者中IL18启动子SNP与T1D易感性之间存在关联。

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