Shakeri H, Khoshi A, Kaffash Bajestani M, Farahi A, Javadzadeh M S, Hosseini Z, Mohammadi R
North Khorasan University of Medical Sciences, School of Medicine - Dept. of Endocrinology - Bojnurd, Iran.
North Khorasan University of Medical Sciences, School of Medicine - Dept. of Clinical Biochemistry - Bojnurd, Iran.
Acta Endocrinol (Buchar). 2019 Jul-Sep;15(3):317-322. doi: 10.4183/aeb.2019.317.
Insulin receptor substrate-1 (IRS-1) has an important role in insulin signaling and the common Gly971Arg polymorphism is related to type 2 diabetes (T2D). IRS-1 Gly971Arg polymorphism can modify tyrosine phosphorylation at a specific site of IRS-1 and may have a critical role in the development of insulin resistance (IR).
The purpose of this study was to investigate the association between this polymorphism and IR in Iranian patients with newly-diagnosed type 2 diabetes.
The study was conducted on 114 individuals with newly-diagnosed T2D and 118 healthy matched controls, aged 20-80 years. Fasting blood glucose and insulin were measured by the enzymatic method and enzyme-linked immunosorbent assay, respectively. Insulin-resistance was calculated by homeostasis model assessment estimated-insulin resistance (HOMA-IR). The gene polymorphism was examined by polymerase chain reaction-restriction fragment length polymorphism.
There are significant differences between IRS1 Gly971Arg polymorphism and studied individuals (P<0.0001). The findings showed that the risk of developing T2D in individuals who had R-alleles was 3.74 folds higher than those without R-alleles. However, IRS1 Gly971Arg polymorphism was not associated with high HOMA-IR, high BMI and familial history of diabetes.
Even though there was not a significant relationship between IRS-1 G971R polymorphism with insulin resistance and high BMI, this polymorphism was correlated to newly-diagnosed diabetic patients. Thus, the evaluation of IRS-1 G971R polymorphism may be helpful for predicting T2D new cases.
胰岛素受体底物-1(IRS-1)在胰岛素信号传导中起重要作用,常见的Gly971Arg多态性与2型糖尿病(T2D)有关。IRS-1 Gly971Arg多态性可改变IRS-1特定位点的酪氨酸磷酸化,可能在胰岛素抵抗(IR)的发生发展中起关键作用。
本研究旨在探讨这种多态性与伊朗新诊断2型糖尿病患者IR之间的关联。
该研究对114例新诊断的T2D患者和118例年龄在20-80岁的健康匹配对照进行。分别采用酶法和酶联免疫吸附测定法测量空腹血糖和胰岛素。通过稳态模型评估估计胰岛素抵抗(HOMA-IR)计算胰岛素抵抗。采用聚合酶链反应-限制性片段长度多态性检测基因多态性。
IRS1 Gly971Arg多态性与研究对象之间存在显著差异(P<0.0001)。研究结果表明,携带R等位基因的个体患T2D的风险比未携带R等位基因的个体高3.74倍。然而,IRS1 Gly971Arg多态性与高HOMA-IR、高BMI和糖尿病家族史无关。
尽管IRS-1 G971R多态性与胰岛素抵抗和高BMI之间没有显著关系,但这种多态性与新诊断的糖尿病患者相关。因此,评估IRS-1 G971R多态性可能有助于预测T2D新病例。