• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1080/10641960801949909
PMID:18293164
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。

相似文献

1
Two polymorphisms in NEDD4L gene and essential hypertension in Chinese Hans - a population-based case-control study.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
Clin Exp Hypertens. 2008 Feb;30(2):87-94. doi: 10.1080/10641960801949909.
2
Gender difference in association of NEDD4L gene variants among southern Han Chinese with essential hypertension - a population-based case-control study.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。
Clin Exp Hypertens. 2014;36(5):309-14. doi: 10.3109/10641963.2013.827693. Epub 2013 Sep 18.
3
[Association between rs4149601 polymorphism and essential hypertension in Kazakh].[哈萨克族rs4149601基因多态性与原发性高血压的关联]
Zhonghua Xin Xue Guan Bing Za Zhi. 2010 Oct;38(10):918-22.
4
A Variant in the NEDD4L Gene Associates With Hypertension in Chronic Kidney Disease in the Southeastern Han Chinese Population.NEDD4L 基因变异与汉族慢性肾脏病患者高血压相关。
Am J Hypertens. 2020 Apr 1;33(4):341-349. doi: 10.1093/ajh/hpaa015.
5
Association of variants in NEDD4L with blood pressure response and adverse cardiovascular outcomes in hypertensive patients treated with thiazide diuretics.噻嗪类利尿剂治疗的高血压患者中 NEDD4L 变异与血压反应和不良心血管结局的关联。
J Hypertens. 2013 Apr;31(4):698-704. doi: 10.1097/HJH.0b013e32835e2a71.
6
[Association of the rs4149601 polymorphism of NEDD4L gene with obesity in Xinjiang Kazakh population].[NEDD4L基因rs4149601多态性与新疆哈萨克族人群肥胖的相关性]
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Dec;27(6):668-71. doi: 10.3760/cma.j.issn.1003-9406.2010.06.014.
7
A functional variant of NEDD4L is associated with obesity and related phenotypes in a Han population of Southern China.NEDD4L的一个功能性变体与中国南方汉族人群的肥胖及相关表型有关。
Int J Mol Sci. 2013 Apr 2;14(4):7433-44. doi: 10.3390/ijms14047433.
8
Genetic variation of NEDD4L is associated with essential hypertension in female Kazakh general population: a case-control study.NEDD4L 的遗传变异与哈萨克族女性原发性高血压的相关性:一项病例对照研究。
BMC Med Genet. 2009 Dec 9;10:130. doi: 10.1186/1471-2350-10-130.
9
[Relationship between rs3865418 polymorphism of neural precursor cell expressed developmentally downregulated 4-like gene and obesity in Kazakh general population].神经前体细胞表达发育性下调基因4样基因rs3865418多态性与哈萨克族普通人群肥胖的关系
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2011 Oct;33(5):533-7.
10
24-h ambulatory blood pressure is linked to chromosome 18q21-22 and genetic variation of NEDD4L associates with cross-sectional and longitudinal blood pressure in Swedes.24小时动态血压与18号染色体q21 - 22区域相关,并且在瑞典人中,NEDD4L基因变异与横断面和纵向血压有关。
Kidney Int. 2006 Aug;70(3):562-9. doi: 10.1038/sj.ki.5001590. Epub 2006 Jun 21.

引用本文的文献

1
NEDD4L is a promoter for angiogenesis and cell proliferation in human umbilical vein endothelial cells.NEDD4L 促进人脐静脉内皮细胞的血管生成和细胞增殖。
J Cell Mol Med. 2024 Apr;28(8):1-11. doi: 10.1111/jcmm.18233.
2
Research progress of Nedd4L in cardiovascular diseases.Nedd4L在心血管疾病中的研究进展
Cell Death Discov. 2022 Apr 16;8(1):206. doi: 10.1038/s41420-022-01017-1.
3
The Renal Physiology of Pendrin-Positive Intercalated Cells.醛固酮诱导的顶端钠依赖性氯/碳酸氢根交换调控盐皮质激素受体阳性肾集合管闰细胞的功能
Physiol Rev. 2020 Jul 1;100(3):1119-1147. doi: 10.1152/physrev.00011.2019.
4
The Role of Intercalated Cell in BP Regulation, Ion Transport, and Transporter Expression.闰细胞在血压调节、离子转运和转运体表达中的作用。
J Am Soc Nephrol. 2018 Jun;29(6):1706-1719. doi: 10.1681/ASN.2017080826. Epub 2018 May 17.
5
Nedd4-2 haploinsufficiency causes hyperactivity and increased sensitivity to inflammatory stimuli.Nedd4-2 杂合不足导致多动和对炎症刺激的敏感性增加。
Sci Rep. 2016 Sep 8;6:32957. doi: 10.1038/srep32957.
6
Genomic Study of Cardiovascular Continuum Comorbidity.心血管连续共病的基因组研究
Acta Naturae. 2015 Jul-Sep;7(3):89-99.
7
NEDD4-2 (NEDD4L): the ubiquitin ligase for multiple membrane proteins.NEDD4-2(NEDD4样蛋白):多种膜蛋白的泛素连接酶。
Gene. 2015 Feb 15;557(1):1-10. doi: 10.1016/j.gene.2014.11.051. Epub 2014 Nov 26.
8
A functional variant of NEDD4L is associated with obesity and related phenotypes in a Han population of Southern China.NEDD4L的一个功能性变体与中国南方汉族人群的肥胖及相关表型有关。
Int J Mol Sci. 2013 Apr 2;14(4):7433-44. doi: 10.3390/ijms14047433.
9
Genetic variation and association analyses of NEDD4 gene in Kazak Chinese patients with hypertension.哈萨克族高血压患者中NEDD4基因的遗传变异与关联分析
Int J Mol Epidemiol Genet. 2010 Jun 20;1(3):226-35.
10
Intracellular ubiquitylation of the epithelial Na+ channel controls extracellular proteolytic channel activation via conformational change.细胞内泛素化上皮钠离子通道通过构象变化控制细胞外蛋白水解通道的激活。
J Biol Chem. 2011 Jan 28;286(4):2416-24. doi: 10.1074/jbc.M110.176156. Epub 2010 Nov 17.