首页> 美国卫生研究院文献>Frontiers in Pharmacology >Intensive Glucose Control Reduces the Risk Effect of TRIB3, SMARCD3, and ATF6 Genetic Variation on Diabetic Vascular Complications
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Intensive Glucose Control Reduces the Risk Effect of TRIB3, SMARCD3, and ATF6 Genetic Variation on Diabetic Vascular Complications

机译:强化血糖控制可降低TRIB3,SMARCD3和ATF6遗传变异对糖尿病性血管并发症的风险作用

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摘要

Type 2 diabetes mellitus is a complex disease. Our previous study revealed that TRIB3 genetic variations were strongly associated with diabetic vascular complications, although TRIB3 regulation pathways remain poorly understood. We used two extreme treatment groups from a 2 × 2 factorial randomized controlled trial to identify a positive association, which was further validated in patients receiving cross treatment to test the effect of genetic polymorphisms among the different treatment groups. A gene-centric score (GS)-weighted model including the three associated genetic variations TRIB3 rs2295490, ATF6 rs12086247, and SMARCD3 rs58125572 was used. The results of the GS model indicated a 46% reduction in the risk of primary vascular complications in patients bearing more than two risk alleles [hazard ratio (HR) 0.54, 95% confidence interval (CI) 0.38–0.76, p < 0.001], following intensive glucose control treatment when compared with patients who received standard glucose control treatment. Furthermore, these patients benefited from active blood pressure-lowering treatment (HR 0.39, 95% CI 0.24–0.64, p < 0.001). However, no significant difference was observed between the two interventions in patients with fewer than two risk alleles (HR 1.09, 95% CI 0.86–1.39, p = 0.47). These results indicate that genetic variants in these three genes may be useful biomarkers for individualized drug therapy in diabetic patients.
机译:2型糖尿病是一种复杂的疾病。我们先前的研究表明,TRIB3的遗传变异与糖尿病性血管并发症密切相关,尽管对TRIB3的调控途径知之甚少。我们使用来自2×2析因随机对照试验的两个极端治疗组来鉴定阳性关联,这在接受交叉治疗的患者中得到了进一步验证,以测试不同治疗组之间遗传多态性的影响。使用了以基因为中心的分数(GS)加权模型,该模型包含三个相关的遗传变异TRIB3 rs2295490,ATF6 rs12086247和SMARCD3 rs58125572。 GS模型的结果表明,携带两个以上风险等位基因的患者原发性血管并发症的风险降低了46%[风险比(HR)0.54,95%置信区间(CI)0.38-0.76,p <0.001],与接受标准血糖控制治疗的患者相比,强化血糖控制治疗后的患者。此外,这些患者受益于主动降压治疗(HR 0.39,95%CI 0.24-0.64,p <0.001)。然而,对于少于两个风险等位基因的患者,两种干预措施之间没有观察到显着差异(HR 1.09,95%CI 0.86-1.39,p = 0.47)。这些结果表明,这三个基因的遗传变异可能是糖尿病患者个体化药物治疗的有用生物标记。

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