Background: Diabetic dyslipidemia is a primary contributor to mortality from coronary artery disease (CAD). It is prevalent in diabetic patients and manifests as an elevation of triglyceride (TG) alongside reduced high-density lipoprotein (HDL) concentrations. Both genetic and environmental factors influence the onset of dyslipidemia in type 2 diabetes mellitus (T2DM). The current study aimed to evaluate the involvement of the IRS-1 Gly 972 Arg gene polymorphism in the development of dyslipidemia in type 2 Iraqi diabetics Methods: Two hundred type 2 Iraqi diabetics were recruited, 105 patients with dyslipidemia and 95 without. The IRS-1 gene was analyzed for Gly 972 Arg single nucleotide polymorphism (SNP) by PCR-RFLP. Results: The codominant models explored a significant (OR = 4.4, CI 95% = 1.4 – 13.9, P = 0.01) increase of carriers of the GA genotype in the group of diabetics with dyslipidemia compared to those without. The dominant models highlighted a significant (OR = 4.7, P = 0.008, CI 95% = 1.5 – 14.8) rise of carriers of the variant allele in the group of diabetics with dyslipidemia when compared with those of diabetic patients without. The distribution of the investigated phenotypes was analyzed in relevance to the genotypes of the dominant model (GA + AA vs GG). There were significant (P = 0.01 – 0.006) elevations of fasting serum glucose (FSG), glycosylated haemoglobin (HbA1c), TC, TG, very-low-density lipoprotein (VLDL), and low-density lipoprotein (LDL), concentrations in carriers of the GA+ AA genotypes when compared with those of the GG genotypes. However, IRS-1 concentration was significantly (P = 0.04) decreased in the group of GA+AA carriers compared to those of the GG carriers. Conclusions: Type 2 Iraqi diabetics who carry the variant allele of the rs1801278 SNP of the IRS1 gene are fourfold more susceptible to dyslipidemia compared to those who have the wild allele. Moreover, metabolic changes are relevant to the analyzed SNP.
Read full abstract