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首页> 外文期刊>Clinical and experimental hypertension: CEH >Two polymorphisms in NEDD4L gene and essential hypertension in Chinese Hans - a population-based case-control study.
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Two polymorphisms in NEDD4L gene and essential hypertension in Chinese Hans - a population-based case-control study.

机译:NEDD4L基因的两个多态性与中国汉族人的原发性高血压-基于人群的病例对照研究。

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Neural precursor cell expressed developmentally down-regulated 4-like (NEDD4L) gene may play an important role in the development of hypertension by regulating the amiloride-sensitive epithelial sodium channel for sodium reabsorption. Recently, a functional polymorphism located at the last nucleotide of exon 1 (rs4149601) of the NEDD4L gene were found to be associated with hypertension both in African Americans and whites, and a "flip-flop" association with hypertension was found in two white samples for a polymorphism located at intron 13 (rs3865418). In this study, we aimed at examining the role of these two variants on essential hypertension in Chinese Hans. In a population-based association study, we observed significantly higher prevalence of T allelic frequencies (p = 0.023) in hypertensives than normotensives. In logistic regression analysis, the stronger association was found under the additive model with an odds ratio of 1.31 (1.04-1.67) for T allele (p = 0.025). The association remained significant (p = 0.039) with an odds ratio of 1.29 (1.01-3.66) when adjusting for age and sex. We also constructed an ANCOVA factorial model by using clinical parameters as the dependent variable for rs3865418 polymorphisms. A significantly higher diastolic blood pressure was observed at rs3865418 in the dominant model for the T allele (p = 0.009). The positive association still exist after controlling age and sex (p = 0.013). For rs4149601 polymorphism, however, we did not observe a positive association with hypertension by implicating either logistic regression models or ANCOVA models. Thus, our results support rs3865418 but not rs4149601 polymorphism of NEDD4L gene implicated in the prevalence of hypertension in Chinese Hans.
机译:通过调节阿米洛利敏感的上皮钠通道进行钠的重吸收,神经前体细胞表达的发育性下调的4-like(NEDD4L)基因可能在高血压的发展中起重要作用。最近,发现在黑人和白人中,位于NEDD4L基因第1外显子的最后一个核苷酸(rs4149601)的功能多态性与高血压有关,并且在两个白人样本中发现与高血压有关的“人字拖”现象位于内含子13(rs3865418)的多态性。在这项研究中,我们旨在研究这两种变异对中国汉族人原发性高血压的作用。在一项基于人群的关联研究中,我们观察到高血压中T等位基因频率的患病率(p = 0.023)明显高于正常血压。在逻辑回归分析中,在加性模型下发现T等位基因的比值比为1.31(1.04-1.67),关联性更强(p = 0.025)。调整年龄和性别后,关联性仍然很显着(p = 0.039),比值比为1.29(1.01-3.66)。我们还通过使用临床参数作为rs3865418多态性的因变量构建了ANCOVA阶乘模型。在T等位基因的显性模型中,在rs3865418处观察到舒张压明显升高(p = 0.009)。在控制了年龄和性别之后,仍存在正向关联(p = 0.013)。但是,对于rs4149601多态性,我们没有通过暗示逻辑回归模型或ANCOVA模型与高血压呈正相关。因此,我们的结果支持NEDD4L基因的rs3865418,但不支持rs4149601多态性,与中国汉族高血压的患病率有关。

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