DISTRIBUTION OF KCNJ11 E23K POLYMORPHISM IN VIETNAMESE POPULATION AND ITS ASSOCIATION WITH HYPERGLYCEMIA

Thi Thu Nguyen, Quang Binh Tran
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Abstract

Background: KCNJ11 gene, encoding ATP-sensitive channel subunits, involves in insulin secretion. The study aimed at investigating the distribution of the KCNJ11 E23K (rs5219) polymorphism and its association with prediabetes and type 2 diabetes (T2D) in Vietnamese population. Methods: A cross-sectional study randomly recruited 2.676 participants aged 40-64 years from a general population in Ha Nam province, Vietnam. Glycemic status of the subjects was classified based on fasting plasma glucose and oral glucose tolerance test. PCR-restriction fragment length polymorphism method was applied to detect the KCNJ11-rs5219 polymorphism. Genotype frequencies were compared to find the distribution difference among normoglycemic, prediabetes, and T2D groups. Generalized linear models and multinomial logistic regression analysis were used to determine the associations of the KCNJ11-rs5219 polymorphism with prediabetes and T2D. Results: The frequencies of minor K allele in normoglycemic, prediabetes and T2D groups were 33.2, 32.6 and 35.4%, respectively. Genotypic distribution of the E23K polymorphism was in Hardy-Weinberg equilibrium and not significantly different among the three glucose groups (p > 0.05). Fasting plasma glucose and 2-h glucose levels were not significantly different among three genotypes EE, EK, and KK (p > 0.05). After adjusted for age, sex, anthropometric and environmental factors, no significant association was found between the KCNJ11-rs5219 polymorphism and prediabetes or T2D with ORs from 0.80 to 1.29. Conclusion: The minor K allele was predominant and genotype frequency in the population was remained constant among generations. The study suggests no significant association beween the KCNJ11-rs5219 polymorphism and hyperglycemia in the Vietnamese population.
越南人群kcnj11 e23k多态性分布及其与高血糖的关系
背景:KCNJ11基因编码atp敏感通道亚基,参与胰岛素分泌。本研究旨在调查越南人群中KCNJ11 E23K (rs5219)多态性的分布及其与糖尿病前期和2型糖尿病(T2D)的关系。方法:采用横断面研究方法,从越南河南省的普通人群中随机招募2676名年龄在40-64岁之间的参与者。根据空腹血糖和口服糖耐量试验对受试者的血糖状态进行分类。采用pcr -限制性片段长度多态性方法检测KCNJ11-rs5219多态性。比较基因型频率在血糖正常组、糖尿病前期组和T2D组之间的分布差异。采用广义线性模型和多项逻辑回归分析来确定KCNJ11-rs5219多态性与糖尿病前期和T2D的关系。结果:轻度K等位基因在血糖正常组、糖尿病前期组和T2D组的频率分别为33.2%、32.6%和35.4%。E23K多态性的基因型分布符合Hardy-Weinberg平衡,3个葡萄糖组间差异不显著(p > 0.05)。EE、EK、KK三种基因型患者的空腹血糖和2小时血糖水平无显著差异(p > 0.05)。在调整了年龄、性别、人体测量和环境因素后,KCNJ11-rs5219多态性与前驱糖尿病或T2D之间无显著相关性,or为0.80 ~ 1.29。结论:小K等位基因在人群中占主导地位,基因型频率在世代间保持不变。该研究提示越南人群中KCNJ11-rs5219多态性与高血糖无显著关联。
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