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Associations of MTHFR and MTRR polymorphisms with serum lipid levels in chinese hypertensive patients

机译:中国高血压患者MTHFR和MTRR基因多态性与血脂水平的关系

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Objective: To examine the effects of the methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) gene polymorphisms and their interactions with environmental factors on serum lipid levels. Methods: We investigated totally 340 patients with essential hypertension, from Dongzhi community, Anhui, China. High-throughput TaqMan allelic discrimination assay was used for the genotyping of MTHFR C677T (Ala222Val), MTHFR A1298C (Glu429Ala), MTRR A66G (Ile22Met), and MTRR His595Tyr. Results: Compared with the MTRR 66AA genotype carriers, the GG genotype carriers had lower serum total cholesterol (TC) levels (adjusted β ± standard error [SE]: -0.5 ± 0.2 mmol/L; P =.003) and low-density lipoprotein cholesterol (LDL-C) levels (adjusted β ± SE: -0.4 ± 0.2 mmol/L; P =.005). Their false discovery rate (FDR)-adjusted P values were 0.056 and 0.056, respectively. We further found that there was a statistically significant interaction between 677TT genotype and sex in their associations with LDL levels (P interaction =.020), and significant interaction between 677TT genotype and smoking on LDL levels (P interaction =.036). A similar pattern of interaction was found between 66GG and drinking on levels of TC (P interaction =.034) and LDL (P interaction =.020). However, there were no significant interactions observed after FDR adjustment. Conclusion: Both MTHFR and MTRR gene polymorphisms could be important genetic determinants of serum lipid levels in Chinese patients with hypertension. These findings need to be replicated in a larger sample.
机译:目的:研究亚甲基四氢叶酸还原酶(MTHFR)和蛋氨酸合酶还原酶(MTRR)基因多态性及其与环境因素的相互作用对血脂水平的影响。方法:我们对来自安徽省东直社区的340例原发性高血压患者进行了调查。使用高通量TaqMan等位基因鉴别测定法对MTHFR C677T(Ala222Val),MTHFR A1298C(Glu429Ala),MTRR A66G(Ile22Met)和MTRR His595Tyr进行基因分型。结果:与MTRR 66AA基因型携带者相比,GG基因型携带者具有较低的血清总胆固醇(TC)水平(校正后的β±标准误差[SE]:-0.5±0.2 mmol / L; P = .003)和低密度脂蛋白胆固醇(LDL-C)水平(调整后的±±SE:-0.4±0.2 mmol / L; P = .005)。他们的错误发现率(FDR)调整后的P值分别为0.056和0.056。我们进一步发现,在677TT基因型和性别与LDL水平的关联中,存在统计学上的显着相互作用(P相互作用= .020),在677TT基因型与吸烟之间在LDL水平上具有显着的相互作用(P相互作用= .036)。在66GG和饮酒的TC(P相互作用= .034)和LDL(P相互作用= .020)水平之间发现了相似的相互作用模式。但是,FDR调整后没有观察到明显的相互作用。结论:MTHFR和MTRR基因多态性可能是中国高血压患者血脂水平的重要遗传决定因素。这些发现需要在更大的样本中复制。

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