Insulin receptor substrate 1 gene variations and lipid profile characteristics in the type 2 diabetic patients with comorbid obesity and chronic pancreatitis.

Q3 Medicine Endocrine regulations Pub Date : 2022-02-18 DOI:10.2478/enr-2022-0001
Mariya Marushchak, Uliana Hevko, Inna Krynytska
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引用次数: 1

Abstract

Objective. Type 2 diabetes mellitus (T2DM) is one of diseases that develops in a setting of polymorbid processes or more often promotes their development, forming in this spectrum the phenomenon of comorbidity. The aim of this study was to evaluate changes in the lipid panel data in T2DM patients with comorbid obesity and chronic pancreatitis (CP) taking into account the C/A polymorphism of the insulin receptor substrate 1 (IRS1) gene (rs2943640). Methods. The study involved 34 T2DM patients and 10 healthy individuals. The rs2943640 IRS1 gene polymorphism was genotyped using the TaqMan real-time polymerase chain reaction (PCR) method. Blood serum lipid panel data were determined with commercially available kits on a Cobas 6000 analyzer. Results. In patients with only T2DM and T2DM + comorbid obesity, an association between IRS1 gene polymorphism (rs2943640) and lipid profile abnormalities with maximum changes of the lipid characteristics recorded in C/C genotype carriers was found. Within the C/C genotype of the IRS1 gene (rs2943640) in type 2 diabetic patients with comorbid obesity and CP, significantly lower high-density lipoprotein cholesterol (HDL-C) levels and significantly higher levels of triglycerides (TG), non-HDL-C and remnant cholesterol (RC) in relation to type 2 diabetic patients with comorbid obesity were found. At the same time, within the C/A genotype of the IRS1 gene (rs2943640), significant changes of lipid panel data were found in type 2 diabetic patients with comorbid obesity relative to the control group (p<0.001). Conclusions. Our data indicate that the presence of the C allele of IRS1 gene (rs2943640) in both homozygous and heterozygous states may indicate increased risk of dyslipidemia in type 2 diabetic patients with comorbidities.

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2型糖尿病合并肥胖和慢性胰腺炎患者胰岛素受体底物1基因变异和脂质谱特征
目标。2型糖尿病(T2DM)是一种在多病过程中发展的疾病,或者更经常地促进它们的发展,在这一谱系中形成合并症现象。本研究的目的是在考虑胰岛素受体底物1 (IRS1)基因(rs2943640)的C/A多态性的情况下,评估合并肥胖和慢性胰腺炎(CP)的T2DM患者脂质面板数据的变化。方法。该研究涉及34名2型糖尿病患者和10名健康人。采用TaqMan实时聚合酶链反应(PCR)方法对rs2943640 IRS1基因多态性进行基因分型。采用市售试剂盒,在Cobas 6000分析仪上测定血清脂质板数据。结果。在仅有T2DM和T2DM +合并肥胖的患者中,发现IRS1基因多态性(rs2943640)与脂质异常之间存在关联,C/C基因型携带者记录的脂质特征变化最大。2型糖尿病合并肥胖和CP患者IRS1基因(rs2943640)的C/C基因型中,高密度脂蛋白胆固醇(HDL-C)水平显著低于2型糖尿病合并肥胖患者,甘油三酯(TG)、非HDL-C和残余胆固醇(RC)水平显著高于2型糖尿病合并肥胖患者。同时,在IRS1基因(rs2943640)的C/A基因型中,2型糖尿病合并肥胖患者的脂质面板数据相对于对照组发生了显著变化(p结论。我们的数据表明,IRS1基因C等位基因(rs2943640)在纯合子和杂合子状态下的存在可能表明伴有合并症的2型糖尿病患者血脂异常的风险增加。
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来源期刊
Endocrine regulations
Endocrine regulations Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.70
自引率
0.00%
发文量
33
审稿时长
8 weeks
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