Association of KCNJ11 gene (rs5219) polymorphism with HOMA-IR and HOMA B values in type 2 diabetes mellitus in India: A case-control study

Objectives Type 2 diabetes mellitus (T2DM) is a complex illness that results from either insulin resistance or insufficient insulin, which raises blood sugar levels. Numerous genes interact to influence the secretion of insulin. A gene of great interest is KCNJ11 of subfamily-J, member 11, which functions as an inwardly rectifying ATP-sensitive potassium (KATP) channel in pancreatic beta cells and is involved in glucose-stimulated insulin release. Material and Methods The present case-control study attempts to delineate the genetic impact of KCNJ11 (rs5219) gene polymorphism on the risk of T2DM in the Indian population. It involves 55 patients with type 2 diabetes (fasting plasma glucose of >126 mg/dl, 2-h glucose of >200 mg/dl, or HbA1c level of >6.4%) and 55 healthy controls (fasting plasma glucose of <100 mg/dl, 2-h glucose of <140 mg/dl, or HbA1c level of <6.4%). polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP) was used to study KCNJ11 polymorphism through a standard protocol. Enzyme Linked Immunosorbent Assay (ELISA) was used to estimate serum Insulin levels. HOMA-IR & HOMA-β values were calculated. Statistical analysis was done using t -test, Chi-Square test, and One-way analysis of variance (ANOVA) test. Results Serum insulin levels and HOMA-IR values were significantly decreased in cases than in the control group. Logistic regression analysis showed that the frequency of KK genotype in T2DM individuals (21.8%) was higher than the control group (9%) ( p = 0.01). Frequency of K allele (38%) in patients was higher than the control group (18%) ( p = 0.001). The K allele risk in diabetic patients was 9.9 times higher as compared to controls ( p = 0.001, OR 9.9, 95%Cl 0.036–0.36). Homeostatic model assessment β (HOMA-β) values of KK genotype (59.9±27.8315) were lower than that of EK (76.8±33.23) and EE (127.9±44.59) genotypes ( p < 0.001). Conclusion The presence of KCNJ11 (rs 5219) gene polymorphism shows a noteworthy correlation with the likelihood of developing T2DM among the North Indian population. K allele is more likely to be present in individuals with T2DM than the control group. Moreover, HOMA-β values of those with the KK genotype were found to be lower than the individuals having EK and EE genotypes.

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Journal
Annals of the National Academy of Medical Sciences (India)
Published
2024-08-26
DOI
https://doi.org/10.25259/anams-2023-4-15-(912)
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1
Primary Topic
Pancreatic function and diabetes
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article
Field-Weighted Citation Impact
0.57
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article

Association of KCNJ11 gene (rs5219) polymorphism with HOMA-IR and HOMA B values in type 2 diabetes mellitus in India: A case-control study

Alka Ramteke, Charanjeet Kaur, Sukanya Gangopadhyay, Md Muntakhab et al.
1 citations
Annals of the National Academy of Medical Sciences (India)
Pancreatic function and diabetes
0.57
article

Association of KCNJ11 gene (rs5219) polymorphism with HOMA-IR and HOMA B values in type 2 diabetes mellitus in India: A case-control study

Alka Ramteke, Charanjeet Kaur, Sukanya Gangopadhyay, Md Muntakhab, Shilpa Suneja
article en
1 citations

Abstract

Objectives Type 2 diabetes mellitus (T2DM) is a complex illness that results from either insulin resistance or insufficient insulin, which raises blood sugar levels. Numerous genes interact to influence the secretion of insulin. A gene of great interest is KCNJ11 of subfamily-J, member 11, which functions as an inwardly rectifying ATP-sensitive potassium (KATP) channel in pancreatic beta cells and is involved in glucose-stimulated insulin release. Material and Methods The present case-control study attempts to delineate the genetic impact of KCNJ11 (rs5219) gene polymorphism on the risk of T2DM in the Indian population. It involves 55 patients with type 2 diabetes (fasting plasma glucose of >126 mg/dl, 2-h glucose of >200 mg/dl, or HbA1c level of >6.4%) and 55 healthy controls (fasting plasma glucose of <100 mg/dl, 2-h glucose of <140 mg/dl, or HbA1c level of <6.4%). polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP) was used to study KCNJ11 polymorphism through a standard protocol. Enzyme Linked Immunosorbent Assay (ELISA) was used to estimate serum Insulin levels. HOMA-IR & HOMA-β values were calculated. Statistical analysis was done using t -test, Chi-Square test, and One-way analysis of variance (ANOVA) test. Results Serum insulin levels and HOMA-IR values were significantly decreased in cases than in the control group. Logistic regression analysis showed that the frequency of KK genotype in T2DM individuals (21.8%) was higher than the control group (9%) ( p = 0.01). Frequency of K allele (38%) in patients was higher than the control group (18%) ( p = 0.001). The K allele risk in diabetic patients was 9.9 times higher as compared to controls ( p = 0.001, OR 9.9, 95%Cl 0.036–0.36). Homeostatic model assessment β (HOMA-β) values of KK genotype (59.9±27.8315) were lower than that of EK (76.8±33.23) and EE (127.9±44.59) genotypes ( p < 0.001). Conclusion The presence of KCNJ11 (rs 5219) gene polymorphism shows a noteworthy correlation with the likelihood of developing T2DM among the North Indian population. K allele is more likely to be present in individuals with T2DM than the control group. Moreover, HOMA-β values of those with the KK genotype were found to be lower than the individuals having EK and EE genotypes.

Annals of the National Academy of Medical Sciences (India)Vol. 60
Vardhman Mahavir Medical College & Safdarjung Hospital (IN)
Good health and well-being
Openalex Percentile: Top 31%
Pancreatic function and diabetes
0.57
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