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汉族南方人群 NEDD4L 基因变异与原发性高血压的相关性存在性别差异——一项基于人群的病例对照研究。

Gender difference in association of NEDD4L gene variants among southern Han Chinese with essential hypertension - a population-based case-control study.

机构信息

School of Biotechnology, Southern Medical University, Guangzhou , Guangdong Province , People's Republic of China .

出版信息

Clin Exp Hypertens. 2014;36(5):309-14. doi: 10.3109/10641963.2013.827693. Epub 2013 Sep 18.

Abstract

Genetic variation of NEDD4L has been associated with hypertension and related phenotypes with conflicting results, probably attributable to gender-, age- and ethnicity-related variations in its phenotypic expression. We evaluated the association of three representative polymorphisms in NEDD4L (rs2288774, rs3865418 and rs4149601) with essential hypertension (EH) in a community-based sample of men (n = 1029) and women (n = 869) belonging to Han Chinese, Southern China, to probe whether gender interacts with NEDD4L in contributing to the risk of EH. In this population sample, rs4149601 was excluded from further analysis due to deviation from Hardy-Weinberg equilibrium. For two other variants tested, the allele frequencies and genotype distributions did not differ between cases and controls (p > 0.05) when both genders were combined. However, sex-stratified analysis revealed that the distribution of the dominant model of rs2288774 (TC + CC versus TT) and the additive and dominant (CT + TT versus CC) models of rs3865418 differed significantly between cases and controls in men (p = 0.044, 0.041 and 0.016, respectively) but not in women. After adjusting for confounding factors, logistic regression analysis showed that rs2288774 and rs3865418 (in the dominant model) were still significantly associated with EH (rs2288774: OR = 0.73, 95% CI = 0.57-0.95, p = 0.017 and rs3865418: OR = 0.71, 95% CI = 0.55-0.92, p = 0.009) in men. There was a significant interaction between the NEDD4L genotype and gender (p for interaction: 0.046 for rs2288774 and 0.033 for rs3865418). Genetic variation in NEDD4L may have sex-dependent effects in the development of EH in Han Chinese. Previous studies that ignore gender-specific effects in their design and interpretation could have failed to identify a uniform conclusion.

摘要

NEDD4L 的遗传变异与高血压及其相关表型有关,但结果相互矛盾,这可能归因于其表型表达在性别、年龄和种族方面的差异。我们在一个基于社区的汉族男性(n=1029)和女性(n=869)样本中评估了 NEDD4L 中三个代表性多态性(rs2288774、rs3865418 和 rs4149601)与原发性高血压(EH)的相关性,以探讨 NEDD4L 是否与性别相互作用,从而导致 EH 的风险。在这个人群样本中,由于偏离 Hardy-Weinberg 平衡,rs4149601 被排除在进一步分析之外。对于另外两个测试的变体,当合并男女两性时,病例和对照组之间的等位基因频率和基因型分布没有差异(p>0.05)。然而,性别分层分析显示,rs2288774 的显性模型(TC+CC 与 TT)和 rs3865418 的加性和显性(CT+TT 与 CC)模型在男性病例和对照组之间的分布有显著差异(p=0.044、0.041 和 0.016),而在女性中则没有。在调整混杂因素后,逻辑回归分析显示,rs2288774 和 rs3865418(在显性模型中)与 EH 仍然显著相关(rs2288774:OR=0.73,95%CI=0.57-0.95,p=0.017 和 rs3865418:OR=0.71,95%CI=0.55-0.92,p=0.009)。NEDD4L 基因型和性别之间存在显著的交互作用(p 交互作用:rs2288774 为 0.046,rs3865418 为 0.033)。NEDD4L 的遗传变异可能在汉族人群中对 EH 的发生具有性别依赖性影响。以前的研究在设计和解释中忽略了性别特异性效应,因此可能未能得出一致的结论。

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