Key result
KCNJ11 E23K polymorphism shows no association with type 2 diabetes in obese ethnic Papuans.
Why the study?
The pathophysiology of T2DM involves complex gene interactions regulating energy metabolism, with several gene polymorphisms implicated in T2DM onset, but their role in obesity-related T2DM in Papuans was unclear.
Is the E23K KCNJ11 gene polymorphism associated with Type 2 Diabetes Mellitus in obese ethnic Papuans?
Case-Control (n=116)
Yes
Is the E23K KCNJ11 gene polymorphism associated with Type 2 Diabetes Mellitus in obese ethnic Papuans?
The E23K KCNJ11 gene polymorphism does not differ in frequency between obese T2DM and non-DM Papuans, though specific genotypes correlate with metabolic parameters.
May not support KCNJ11 E23K as T2DM risk factor in obese Papuans; leaves open population-specific genetic associations.
Background: Pathophysiology of type 2 diabetes mellitus (T2DM) is influenced by the complex interaction of several genes that regulate energy metabolism in the body. Several polymorphisms that occur in many gene encode components of glucose metabolism regulation are significantly implicated in the onset of T2DM.Methods: This case-control study. Case group with 58 subjects of T2DM patients with obesity and a control group with 58 subjects of non-DM obese patients from ethnic Papuans in Jayapura city, Indonesia.Results: The results of the genotype frequency distribution (AA, GA, GG) and allele (A and G) showed statistically no significant differences. The relationship of anthropometry and blood chemical parameters with genotype (AA-GA-GG) gene potassium inwardly rectifying channel sub family J member 11 (KCNJ11) showed no statistically significant difference (p>0.05). The relationship of anthropometry and blood chemical parameters of genotype (AA-GA) gene KCNJ11 indicated that diastolic blood pressure variables, glucose, triglyceride, high density lipoprotein (HDL), insulin levels, homeostatic model assessment (HOMA) β, and insulin resistance (IR) had statistically significant differences.Conclusions: There is no difference in frequency between genotypes and alleles of the gene KCNJ11 in the T2DM and non-DM group with obesity. There is a link between genotypes of the gene KCNJ11 and T2DM occurrence. As for the combined analysis between blood chemical parameters and genotypes of gene KCNJ11, there is a relationship between genotypes of the gene KCNJ11 and the incidence of T2DM in LDL variables, where the coefficient interval value increases in patients with T2DM.
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Maay et al. (2021) conducted a case-control in Type 2 Diabetes Mellitus with obesity (n=116). E23K gene KCNJ11 polymorphism vs. Non-diabetic obese controls was evaluated on Frequency of KCNJ11 genotypes (AA-GA vs GG) (OR 1.00, 95% CI 0.061-16.379, p=1). The E23K polymorphism of the KCNJ11 gene showed no significant association with type 2 diabetes mellitus in obese ethnic Papuans, with identical genotype frequencies between cases and controls (OR 1.00).
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