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首页> 外文期刊>The Egyptian Rheumatologist >Association of interferon-γ and its (+874 T/A) gene polymorphism with type 2 diabetes mellitus in rheumatoid arthritis patients
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Association of interferon-γ and its (+874 T/A) gene polymorphism with type 2 diabetes mellitus in rheumatoid arthritis patients

机译:类风湿关节炎患者中干扰素-γ及其(+874 T / A)基因多态性与2型糖尿病的关系

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Background Rheumatoid arthritis (RA) patients are at an increased risk of developing type-2 diabetes mellitus (T2DM) compared to the general population. Interferon-γ (IFN-γ) was found to have a role in both RA and T2DM. Aim of the work To investigate the role of IFN-γ and its +874T/A gene polymorphism in the development of T2DM in RA patients. Patients and methods IFN-γ level and its +874T/A gene polymorphism were investigated in 70 RA patients with T2DM and in 80 without, in addition to 150 healthy controls. Results The level of IFN-γ was significantly higher in RA patients with (465 ± 64.4 pg/ml) and without (219 ± 50.3 pg/ml) T2DM compared to controls (110 ± 18 pg/ml) ( p 0.0001). IFN-γ +874T/A genotyping showed a significant increase in the frequency of AA genotype (42.9%) and a significant decrease in TT genotype (14.2%) in RA patients with T2DM compared to those without; similarly, the frequency of the T-allele was significantly lower ( p 0.05) and the A-allele increased ( p 0.05); however no significant differences in the genotypes distribution were found between non-diabetic RA patients and healthy controls. The TT-genotyped RA patients with (539.6 ± 4 pg/ml) and without (260 ± 59.6 pg/ml) diabetes had higher serum IFN-γ levels compared to other genotypes ( p 0.001), while in controls, no significant difference in IFN-γ levels according to genotype was observed. Conclusions Serum IFN-γ and its gene polymorphism may play a role in the susceptibility of RA patients to T2DM. The homozygous genotypes AA and TT seem to be more commonly associated with diabetes in RA patients with special contribution of the A-allele.
机译:背景与一般人群相比,类风湿关节炎(RA)患者患2型糖尿病(T2DM)的风险增加。发现干扰素-γ(IFN-γ)在RA和T2DM中均起作用。工作目的探讨IFN-γ及其+ 874T / A基因多态性在RA患者T2DM发展中的作用。在70位RA患有T2DM的RA患者和80位无T2DM的RA患者以及150位健康对照中,研究了患者和方法的IFN-γ水平及其+ 874T / A基因多态性。结果与对照组(110±18 pg / ml)相比,有(465±64.4 pg / ml)和没有(219±50.3 pg / ml)T2DM的RA患者的IFN-γ水平显着更高(p <0.0001)。与没有T2DM的RA患者相比,IFN-γ+ 874T / A基因分型显示AA基因型频率显着增加(42.9%),TT基因型显着降低(14.2%)。同样,T等位基因的频率显着降低(p <0.05),而A等位基因的频率升高(p <0.05);然而,非糖尿病性RA患者与健康对照者之间在基因型分布上没有显着差异。与其他基因型相比,患有(539.6±4 pg / ml)且没有(260±59.6 pg / ml)糖尿病的TT基因分型RA患者的血清IFN-γ水平更高(p <0.001),而在对照组中,无显着差异观察到根据基因型的IFN-γ水平。结论血清IFN-γ及其基因多态性可能与RA患者对T2DM的易感性有关。在具有A等位基因特殊贡献的RA患者中,纯合基因型AA和TT似乎更常见于糖尿病。

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