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ABCG1/TCF7L2与2型糖尿病之间的关联:一项基于病例对照研究的干预试验。

Association Between ABCG1/TCF7L2 and Type 2 Diabetes Mellitus: An Intervention Trial Based on a Case-Control Study.

作者信息

Su Yinxia, Shang Bo, Hu Xiaoyuan, Zhang Zhihao, Wang Li, Luo Kun, Yao Hua, Liu Xiangtao, Lu Yaoqin, Jiang Sheng

机构信息

State Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, Urumqi, Xinjiang, China.

School of Medical Engineering and Technology, Xinjiang Medical University, Urumqi, Xinjiang, China.

出版信息

J Diabetes Res. 2025 Feb 26;2025:9356676. doi: 10.1155/jdr/9356676. eCollection 2025.

Abstract

Type 2 diabetes mellitus (T2DM) is the result of both genetic and environmental factors. Environmental factors may contribute to the occurrence and development of T2DM by influencing epigenetic modification. The objective of this study was to explore the potential functions of two SNP-CG sites (rs7901695 of TCF7L2 and cg06500161 of ABCG1) that are most strongly associated with T2DM. Given that Uyghur population has been less studied, we conducted an intervention trial in Uyghur people to provide evidence for personalized health management of T2DM in them. From May to July 2022, 320 patients with T2DM and 332 patients without T2DM were treated with dietary pagoda-based health education intervention. The demographic data were collected before intervention and basic physical biochemical indexes before and after intervention by questionnaire and physical biochemical examination. SNP typing was performed by the TaqMan-MGB probe method, and gene methylation was detected by the pyrosequencing method. The rs7901695 genotype difference of TCF7L2 was statistically significant between the case group and the control group ( < 0.05). After adjusting for covariates (smoking, alcohol consumption, exercise, fasting blood glucose (FPG), obesity, and hypertension), the genotype of rs7901695 in the TCF7L2 gene was associated with genetic susceptibility to T2DM in additive (TC vs. TT, = 0.047; CC vs. TT, = 0.010), dominant ( = 0.015), and recessive ( = 0.039) models. Before intervention, there were significant differences in the intake of water between the case group and the control group ( < 0.05). After intervention, there was statistical significance in the intake of coarse grains, fruits, aquatic products, eggs, dairy products, soy products, nuts, edible oils, and water between the case group and the control group (s < 0.05). Logistic regression analysis showed that methylation of the ABCG1 gene was correlated with T2DM susceptibility after adjustment of covariable before intervention ( = 0.015, odds ratio (OR): 1.023; 95% confidence interval (CI): 1.004~1.041) but not after intervention. Generalized multifactor dimensionality reduction (GMDR) showed that the rs7901695 locus of the TCF7L2 gene and the cg06500161 locus of the ABCG1 gene had interaction with hypertension, dyslipidemia, abdominal obesity, and obesity and also had interaction with drinking, smoking, and exercise. The interaction of the rs7901695 site of the TCF7L2 gene and the cg06500161 site of the ABCG1 gene with environmental factors may increase the risk of T2DM in Uyghurs. The interaction between the cg06500161 site of the ABCG1 gene and environmental factors on T2DM varied with the intervention. The cg06500161 site of ABCG1 may serve as a biomarker to evaluate the effect of T2DM interventions.

摘要

2型糖尿病(T2DM)是遗传和环境因素共同作用的结果。环境因素可能通过影响表观遗传修饰促进T2DM的发生发展。本研究旨在探索与T2DM关联最为紧密的两个单核苷酸多态性-胞嘧啶-鸟嘌呤(SNP-CG)位点[转录因子7样蛋白2(TCF7L2)的rs7901695和三磷酸腺苷结合盒转运体G1(ABCG1)的cg06500161]的潜在功能。鉴于维吾尔族人群相关研究较少,我们对维吾尔族人开展了一项干预试验,为其T2DM的个性化健康管理提供依据。2022年5月至7月,对320例T2DM患者和332例非T2DM患者进行了基于膳食宝塔的健康教育干预。通过问卷调查和体格生化检查收集干预前的人口统计学数据以及干预前后的基本身体生化指标。采用TaqMan-MGB探针法进行SNP分型,焦磷酸测序法检测基因甲基化。TCF7L2的rs7901695基因型在病例组和对照组之间差异有统计学意义(<0.05)。在调整协变量(吸烟、饮酒、运动、空腹血糖(FPG)、肥胖和高血压)后,TCF7L2基因中rs7901695的基因型在加性模型(TC与TT,=0.047;CC与TT,=0.010)、显性模型(=0.015)和隐性模型(=0.039)中与T2DM的遗传易感性相关。干预前,病例组和对照组在水的摄入量上存在显著差异(<0.05)。干预后,病例组和对照组在粗粮、水果、水产品、蛋类、乳制品、豆制品、坚果、食用油和水的摄入量上有统计学意义(s<0.05)。逻辑回归分析显示,干预前调整协变量后,ABCG1基因的甲基化与T2DM易感性相关(=0.015,比值比(OR):1.023;95%置信区间(CI):1.004~1.041),但干预后无相关性。广义多因素降维法(GMDR)显示,TCF7L2基因的rs7901695位点和ABCG1基因的cg06500161位点与高血压、血脂异常、腹型肥胖和肥胖存在交互作用,也与饮酒、吸烟和运动存在交互作用。TCF7L2基因的rs7901695位点和ABCG1基因的cg06500161位点与环境因素的交互作用可能增加维吾尔族人患T2DM的风险。ABCG1基因的cg06500161位点与环境因素在T2DM上的交互作用随干预而变化。ABCG1的cg06500161位点可能作为评估T2DM干预效果的生物标志物。

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