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NEDD4L基因的两个多态性与中国汉族人群原发性高血压——一项基于人群的病例对照研究

Two polymorphisms in NEDD4L gene and essential hypertension in Chinese Hans - a population-based case-control study.

作者信息

Wen Hao, Lin Renyong, Jiao Yi, Wang Fen, Wang Shizhen, Lu Daru, Qian Ji, Jin Li, Wang Xiaofeng

机构信息

First Affiliated Hospital, Xinjiang Medical University, Urumqi, China.

出版信息

Clin Exp Hypertens. 2008 Feb;30(2):87-94. doi: 10.1080/10641960801949909.

Abstract

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.

摘要

神经前体细胞表达的发育下调基因4样蛋白(NEDD4L)基因可能通过调节阿米洛利敏感的上皮钠通道进行钠重吸收,在高血压的发生发展中发挥重要作用。最近,人们发现位于NEDD4L基因外显子1最后一个核苷酸处的功能性多态性(rs4149601)在非裔美国人和白人中均与高血压相关,并且在两个白人样本中发现位于内含子13处的一个多态性(rs3865418)与高血压存在“翻转”关联。在本研究中,我们旨在探讨这两个变异在中国汉族原发性高血压中的作用。在一项基于人群的关联研究中,我们观察到高血压患者中T等位基因频率的患病率显著高于血压正常者(p = 0.023)。在逻辑回归分析中,在加性模型下发现T等位基因的关联更强,比值比为1.31(1.04 - 1.67)(p = 0.025)。在调整年龄和性别后,该关联仍然显著(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一个协方差分析因子模型。在T等位基因的显性模型中,rs3865418处观察到舒张压显著升高(p = 0.009)。在控制年龄和性别后,正相关仍然存在(p = 0.013)。然而,对于rs4149601多态性,我们通过逻辑回归模型或协方差分析模型均未观察到与高血压的正相关。因此,我们的结果支持NEDD4L基因的rs3865418而非rs4149601多态性与中国汉族高血压患病率有关。

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