[The influence of polymorphism the Gly972Arg variant insulin receptor substrate-1 (IRS-1) gene, and G-308A TNF-alpha gene on obesity and insulin resistance in children with obesity].

Beata Pyrzak, Alicja Wiśniewska, Barbara Rymkiewicz-Kluczyńska
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引用次数: 0

Abstract

Unlabelled: Genetic factors play a role in the pathogenesis of insulin resistance in obese subjects. The insulin receptor substrate-1 (IRS-1) and IRS-2 are the most important elements of the insulin-signaling pathways, and mutations in this gene have been reported to play a role in determining insulin resistance, particulary in presence of obesity. The polymorpism of the TNF-a-308 gene is also involved in the development of obesity-related insulin resistance, therefore, we investigated whether the IRS-1 and TNF-a polymorphism can predict conversion to insulin resistance and obesity parameters in children with obesity.

Material and methods: The 70 children with obesity simplex were included in this study (9-18 y.o). The antropometric investigations: weight, height, BMI, SDS for BMI, WHR, sum of 3, 10 skinfolds, and percent of body fat by Slaughter's equation was calculated. In each children after 12 hour overnight fast glucose, insulin, leptin and lipids: triglycerides (Tg), cholesterol total (Chol-T), cholesterol HDL (Chol-HDL), cholesterol LDL (Chol-LDL) were measured. The oral glucose tolerance test was performed and HOMA-IR was calculated.

Results: Two variants of genotypic IRS-1 were obtained: C/C(85.7 %), A/C(14.3%), and 3 variants of TNF-a G/G 68 % A/G 29% A/A 3%. Statistical analysis of anthropometric and biochemical variables in groups C/C, vs A/C and variables between IRS and TNF (G/G, A/G + A/A) groups was performed. We did not find any significant differences between these groups in the t-Student test. The girls heterozygous for the A allele--A/C (IRS) had higher body weight than girls who were homozygous C/C (chi(2) =3.87, Pr>chi(2)=0,048). In smaller children studies, both polymorphism--IRS and TNF seems not to be associated with the degree of obesity and insulin resistance.

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[Gly972Arg变异胰岛素受体底物-1 (IRS-1)基因和G-308A tnf - α基因多态性对肥胖儿童肥胖和胰岛素抵抗的影响]。
未标记:遗传因素在肥胖患者胰岛素抵抗的发病机制中起作用。胰岛素受体底物-1 (IRS-1)和IRS-2是胰岛素信号通路中最重要的元件,据报道,该基因的突变在决定胰岛素抵抗中起作用,特别是在肥胖的情况下。TNF-a-308基因的多态性也参与了肥胖相关胰岛素抵抗的发展,因此,我们研究了IRS-1和TNF-a多态性是否可以预测肥胖儿童转化为胰岛素抵抗和肥胖参数。材料与方法:选取单纯性肥胖儿童70例(9 ~ 18岁)。通过Slaughter's方程计算体重、身高、BMI、BMI的SDS、臀重比、3、10个皮褶的总和和体脂百分比。各组患儿12小时后测空腹血糖、胰岛素、瘦素及血脂:甘油三酯(Tg)、总胆固醇(cholt)、胆固醇高密度脂蛋白(choll -HDL)、胆固醇低密度脂蛋白(choll -LDL)。进行口服糖耐量试验,计算HOMA-IR。结果:获得2个基因型IRS-1变异:C/C(85.7%)、A/C(14.3%)和3个基因型TNF-a G/G 68%、A/G 29%、A/A 3%。对C/C组、vs A/C组及IRS与TNF (G/G、A/G + A/A)组间的人体测量和生化变量进行统计分析。在t-Student检验中,我们没有发现这些组之间有任何显著差异。A等位基因-A/C (IRS)杂合子的女孩体重高于C/C纯合子的女孩(chi(2) =3.87, Pr>chi(2)= 0.048)。在规模较小的儿童研究中,IRS和TNF多态性似乎与肥胖程度和胰岛素抵抗无关。
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