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首页> 外文期刊>International Journal of Medical Sciences >Associations of MMP1, 3, 9 and TIMP3 Genes Polymorphism with Isolated Systolic Hypertension in Chinese Han Population
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Associations of MMP1, 3, 9 and TIMP3 Genes Polymorphism with Isolated Systolic Hypertension in Chinese Han Population

机译:中国汉族人群MMP1、3、9和TIMP3基因多态性与单纯收缩期高血压的相关性

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Background and aims: Large artery stiffness and endothelial dysfunction are the predominant characteristic of isolated systolic hypertension. Recently studies have revealed MMP1, 3, 9 and TIMP3 Genes polymorphism were associated with arterial stiffness, but the relationship with isolated systolic hypertension were not further studied. This study was to investigate the associations of MMP1,3,9 and TIMP3 Genes polymorphism with isolated systolic hypertension. Methods: We identified the genotype of the genes in 503 patients with isolated systolic hypertension, 481 essential hypertension patients with elevated diastolic blood pressure and 244 age-matched normotensive controls for 5 SNPs and detected the brachial-ankle pulse wave velocity, flow-mediated dilatation, endothelin-1 and nitric oxide among the participants. Results: Multinomial logistic analyses showed that the 5A allele of rs3025058(5A/6A) in MMP3 and the T allele of rs3918242(C-1562T) in MMP9 were significantly associated with isolated systolic hypertension after adjusted by age, triglyceride, low-density lipoprotein (PPcorrP=0.009, Pcorr=0.027). The 5A/G/C and 6A/A/T haplotypes were significantly associated with isolated systolic hypertension (Permutation p=0.0258; Permutation p=0.000002). In addition, the brachial-ankle pulse wave velocity of different genotypes for the 5A/6A and C-1562T polymorphisms was significantly highest in 5A or T homozygotes (PPConclusion: MMP3 and MMP9 genes variant seem to contribute to the development of isolated systolic hypertension by affecting arterial stiffness and endothelial function.
机译:背景与目的:大动脉僵硬和内皮功能障碍是孤立性收缩期高血压的主要特征。最近的研究表明,MMP1、3、9和TIMP3基因多态性与动脉僵硬度有关,但与孤立的收缩期高血压的关系尚未进一步研究。本研究旨在探讨MMP1、3、9和TIMP3基因多态性与单纯收缩期高血压的关系。方法:我们鉴定了503例单纯收缩期高血压患者,481例舒张压升高的原发性高血压患者和244例年龄匹配的正常血压控制人群的5个SNP的基因型,并检测了臂踝脉搏波速度,血流介导的扩张,参与者中的内皮素1和一氧化氮。结果:多项逻辑分析表明,经年龄,甘油三酸酯,低密度脂蛋白调节后,MMP3中rs3025058(5A / 6A)的5A等位基因和MMP9中rs3918242(C-1562T)的T等位基因与单纯收缩期高血压显着相关(PPcorrP = 0.009,Pcorr = 0.027)。 5A / G / C和6A / A / T单倍型与孤立的收缩期高血压显着相关(排列p = 0.0258;排列p = 0.000002)。此外,5A / 6A和C-1562T多态性的不同基因型的臂踝脉搏波速度在5A或T纯合子中显着最高(PP结论:MMP3和MMP9基因变异似乎通过分离而导致单纯性收缩期高血压影响动脉僵硬度和内皮功能。

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