Association of SLC30A8 rs13266634 gene polymorphism with type 2 diabetes mellitus (T2DM) in a population of Noakhali, Bangladesh: a case–control study

IF 1.2 Q4 GENETICS & HEREDITY
Farhana Siddiqi Mitu, Md. Murad Hossain, Shuvo Chandra Das, Md. Mafizul Islam, Dhirendra Nath Barman, Shipan Das Gupta
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Abstract

Type 2 diabetes mellitus (T2DM) is considered to be a polygenic disorder that emerges as a result of complicated gene-environment interactions. Several investigations revealed that SLC30A8 rs13266634 polymorphism elevates T2DM risk. T2DM and hypertension (HTN) are often found to be coexist. Compared to normotensive non-diabetic controls, T2DM patients with HTN have a fourfold increased risk of cardiovascular disease (CVD). The average age of T2DM diagnosis is decreasing, and ‘early onset of T2DM’ in adolescents and young adults is an emerging worldwide health concern. The objective of this study was to examine the potential correlations of SLC30A8 rs13266634 polymorphism with T2DM and T2DM-related CVD and HTN as well as ‘early onset of T2DM’ in the Noakhali region. This case–control study involved 163 T2DM patients and 75 healthy controls for analysis of SLC30A8-rs13266634 polymorphism. Genotyping of this polymorphism was performed using polymerase chain reaction-restriction fragment length polymorphism (PCR–RFLP) method. MedCalc and Gene Calc programs were used for statistical analysis. A statistically significant association of SLC30A8 rs13266634 (P < 0.05) with T2DM was found in dominant, over dominant and allele models. But this study found no evidence of a connection between SLC30A8-rs13266634 with CVD, HTN, or ‘early onset of T2DM’ in any models. Furthermore, T2DM patients had higher total cholesterol (TC) and triglyceride (TG) levels than non-diabetics individuals. This study revealed a substantial association between the variation in SLC30A8-rs13266634 and the increased risk of developing T2DM within a sample of the Noakhali population in Bangladesh. However, no significant associations were observed between SLC30A8-rs13266634 and T2DM-related cardiovascular disease (CVD), hypertension (HTN), or the early onset of T2DM within this specific population.
孟加拉国 Noakhali 人口中 SLC30A8 rs13266634 基因多态性与 2 型糖尿病 (T2DM) 的关系:一项病例对照研究
2 型糖尿病(T2DM)被认为是一种多基因疾病,是复杂的基因-环境相互作用的结果。多项研究发现,SLC30A8 rs13266634 多态性会增加 T2DM 风险。T2DM 和高血压(HTN)常常同时存在。与血压正常的非糖尿病对照组相比,患有高血压的 T2DM 患者罹患心血管疾病(CVD)的风险增加了四倍。T2DM 诊断的平均年龄正在下降,青少年和年轻成年人 "T2DM 早发 "已成为全球新出现的健康问题。本研究旨在探讨 SLC30A8 rs13266634 多态性与 T2DM、T2DM 相关心血管疾病和高血压以及努阿卡利地区 "T2DM 早发 "的潜在相关性。这项病例对照研究涉及 163 名 T2DM 患者和 75 名健康对照者,以分析 SLC30A8-rs13266634 多态性。该多态性的基因分型采用聚合酶链式反应-限制性片段长度多态性(PCR-RFLP)方法进行。统计分析使用了 MedCalc 和 Gene Calc 程序。在显性、过显性和等位基因模型中,SLC30A8 rs13266634(P < 0.05)与 T2DM 的关系均有统计学意义。但在任何模型中,本研究都没有发现 SLC30A8-rs13266634 与心血管疾病、高血压或 "T2DM 早发 "有关。此外,与非糖尿病患者相比,T2DM 患者的总胆固醇(TC)和甘油三酯(TG)水平更高。这项研究显示,在孟加拉国努哈里人口样本中,SLC30A8-rs13266634 的变异与 T2DM 患病风险的增加有很大关系。但是,在这一特定人群中,没有观察到 SLC30A8-rs13266634 与 T2DM 相关的心血管疾病(CVD)、高血压(HTN)或 T2DM 早期发病之间有明显的关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Egyptian Journal of Medical Human Genetics
Egyptian Journal of Medical Human Genetics Medicine-Genetics (clinical)
CiteScore
2.20
自引率
7.70%
发文量
150
审稿时长
18 weeks
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