• 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

相似文献

1
Association between -T786C NOS3 polymorphism and resistant hypertension: a prospective cohort study.一氧化氮合酶3基因(NOS3)-T786C多态性与难治性高血压的关联:一项前瞻性队列研究。
BMC Cardiovasc Disord. 2009 Aug 4;9:35. doi: 10.1186/1471-2261-9-35.
2
[Genetic variants of endothelial nitric synthase in gestational hypertension and preeclampsia].[妊娠期高血压疾病和子痫前期中内皮型一氧化氮合酶的基因变异]
Ginekol Pol. 2012 Sep;83(9):652-9.
3
Statistically verified methods for determining predictors of development of arterial hypertension depending on endothelial nitric oxide synthase T786C gene promoter polymorphism using lipid profile indicators.基于血脂指标,采用统计学方法验证内皮型一氧化氮合酶 T786C 基因启动子多态性与动脉高血压发展相关的预测因子。
Endocr Regul. 2024 Jun 11;58(1):138-143. doi: 10.2478/enr-2024-0015. Print 2024 Jan 1.
4
The -786 T/C polymorphism of NOS3 gene is a susceptibility marker of COPD among Tunisians that correlates with nitric oxide levels and airflow obstruction.一氧化氮合酶3(NOS3)基因-786位点的T/C多态性是突尼斯人慢性阻塞性肺疾病(COPD)的一个易感标志物,与一氧化氮水平及气流阻塞相关。
Cytokine. 2017 May;93:66-73. doi: 10.1016/j.cyto.2017.05.010. Epub 2017 May 16.
5
Impact of obesity and nitric oxide synthase gene G894T polymorphism on essential hypertension.肥胖及一氧化氮合酶基因G894T多态性对原发性高血压的影响
J Physiol Pharmacol. 2015 Oct;66(5):681-9.
6
Association of NOS3 gene polymorphisms with essential hypertension in Sudanese patients: a case control study.苏丹患者中一氧化氮合酶3基因多态性与原发性高血压的关联:一项病例对照研究。
BMC Med Genet. 2017 Nov 13;18(1):128. doi: 10.1186/s12881-017-0491-7.
7
Gene variation in resistant hypertension: multilocus analysis of the angiotensin 1-converting enzyme, angiotensinogen, and endothelial nitric oxide synthase genes.抗高血压基因变异:血管紧张素 1 转换酶、血管紧张素原和内皮型一氧化氮合酶基因的多位点分析。
DNA Cell Biol. 2011 Aug;30(8):555-64. doi: 10.1089/dna.2010.1156. Epub 2011 Mar 27.
8
[Single nucleotide polymorphisms in NOS3 A-922G, T-786C and G894T: a correlation study of the distribution of their allelic combinations with hypertension in chinese Han population].[一氧化氮合酶3基因(NOS3)A-922G、T-786C和G894T单核苷酸多态性:中国汉族人群中其等位基因组合分布与高血压的相关性研究]
Yi Chuan. 2006 Jan;28(1):3-10.
9
Correlation of interactions between NOS3 polymorphisms and oxygen therapy with retinopathy of prematurity susceptibility.一氧化氮合酶3(NOS3)基因多态性与氧疗之间的相互作用与早产儿视网膜病变易感性的相关性。
Int J Clin Exp Pathol. 2015 Nov 1;8(11):15250-4. eCollection 2015.
10
Genetic and pharmacogenetic associations between NOS3 polymorphisms, blood pressure, and cardiovascular events in hypertension.高血压患者中一氧化氮合酶3(NOS3)基因多态性、血压与心血管事件之间的遗传及药物遗传学关联
Am J Hypertens. 2009 Jul;22(7):748-53. doi: 10.1038/ajh.2009.81. Epub 2009 Apr 30.

引用本文的文献

1
A genome-wide association study identifies a novel candidate locus at the DLGAP1 gene with susceptibility to resistant hypertension in the Japanese population.一项全基因组关联研究在日本人群中发现了一个新的候选基因 DLGAP1,该基因与耐药性高血压的易感性有关。
Sci Rep. 2021 Sep 30;11(1):19497. doi: 10.1038/s41598-021-98144-z.
2
Genomic Association of Single Nucleotide Polymorphisms with Blood Pressure Response to Hydrochlorothiazide among South African Adults with Hypertension.南非高血压成人中,单核苷酸多态性与氢氯噻嗪血压反应的基因组关联研究
J Pers Med. 2020 Dec 9;10(4):267. doi: 10.3390/jpm10040267.
3
Endothelial nitric oxide synthase gene (T786C and G894T) polymorphisms in Egyptian patients with type 2 diabetes.埃及2型糖尿病患者内皮型一氧化氮合酶基因(T786C和G894T)多态性
J Genet Eng Biotechnol. 2017 Dec;15(2):431-436. doi: 10.1016/j.jgeb.2017.05.001. Epub 2017 Jun 1.
4
Cardiovascular Effects and Benefits of Exercise.运动对心血管系统的影响及益处
Front Cardiovasc Med. 2018 Sep 28;5:135. doi: 10.3389/fcvm.2018.00135. eCollection 2018.
5
Genome-wide study of resistant hypertension identified from electronic health records.基于电子健康记录的顽固性高血压全基因组研究。
PLoS One. 2017 Feb 21;12(2):e0171745. doi: 10.1371/journal.pone.0171745. eCollection 2017.
6
Endothelial nitric oxide synthase gene polymorphisms and prostate cancer risk in Serbian population.塞尔维亚人群内皮型一氧化氮合酶基因多态性与前列腺癌风险的关系。
Int J Exp Pathol. 2013 Dec;94(6):355-61. doi: 10.1111/iep.12045. Epub 2013 Sep 2.
7
Association of the genetic polymorphisms of the ACE gene and the eNOS gene with lupus nephropathy in northern Chinese population.中国北方人群 ACE 基因和 eNOS 基因的遗传多态性与狼疮性肾炎的关系。
BMC Med Genet. 2010 Jun 14;11:94. doi: 10.1186/1471-2350-11-94.

本文引用的文献

1
An association between resistant hypertension and the null GSTM1 genotype.抗性高血压与GSTM1基因无效型之间的关联。
J Hum Hypertens. 2009 Aug;23(8):556-8. doi: 10.1038/jhh.2009.19. Epub 2009 Mar 12.
2
A common variant of the eNOS gene (E298D) is an independent risk factor for left ventricular hypertrophy in human essential hypertension.内皮型一氧化氮合酶基因(E298D)的一种常见变体是人类原发性高血压中左心室肥厚的独立危险因素。
Clin Sci (Lond). 2009 Jun 15;117(2):67-73. doi: 10.1042/CS20080476.
3
Endothelial nitric oxide synthase Glu298Asp, 4b/a, and T-786C polymorphisms in type 2 diabetic retinopathy.2型糖尿病视网膜病变中内皮型一氧化氮合酶Glu298Asp、4b/a及T-786C基因多态性
Clin Endocrinol (Oxf). 2008 Apr;68(4):542-6. doi: 10.1111/j.1365-2265.2007.03089.x. Epub 2007 Oct 31.
4
Three endothelial nitric oxide (NOS3) gene polymorphisms in hypertensive and normotensive individuals: meta-analysis of 53 studies reveals evidence of publication bias.高血压和血压正常个体中三种内皮型一氧化氮合酶(NOS3)基因多态性:53项研究的荟萃分析揭示了发表偏倚的证据。
J Hypertens. 2007 Sep;25(9):1763-74. doi: 10.1097/HJH.0b013e3281de740d.
5
Biochemical consequences of the NOS3 Glu298Asp variation in human endothelium: altered caveolar localization and impaired response to shear.人内皮细胞中一氧化氮合酶3(NOS3)Glu298Asp变异的生化后果:小窝定位改变及对剪切力的反应受损。
FASEB J. 2007 Sep;21(11):2655-63. doi: 10.1096/fj.06-7088com. Epub 2007 Apr 20.
6
Endothelial nitric oxide synthase haplotypes are related to blood pressure elevation, but not to resistance to antihypertensive drug therapy.内皮型一氧化氮合酶单倍型与血压升高有关,但与抗高血压药物治疗的耐药性无关。
J Hypertens. 2006 Dec;24(12):2393-7. doi: 10.1097/01.hjh.0000251899.47626.4f.
7
Association of VEGF and eNOS gene polymorphisms in type 2 diabetic retinopathy.2型糖尿病视网膜病变中血管内皮生长因子(VEGF)与内皮型一氧化氮合酶(eNOS)基因多态性的关联
Mol Vis. 2006 Apr 11;12:336-41.
8
Endothelial nitric oxide synthase genotype and haplotype are not associated with diabetic retinopathy in diabetes type 2 patients.内皮型一氧化氮合酶基因型和单倍型与2型糖尿病患者的糖尿病视网膜病变无关。
Nitric Oxide. 2006 Dec;15(4):417-22. doi: 10.1016/j.niox.2006.02.002. Epub 2006 Apr 3.
9
Association between the CYP3A5 genotype and blood pressure.细胞色素P450 3A5(CYP3A5)基因与血压之间的关联。
Hypertension. 2005 Feb;45(2):294-8. doi: 10.1161/01.HYP.0000151361.31736.96. Epub 2004 Dec 13.
10
Pathogenesis and treatment of resistant hypertension.顽固性高血压的发病机制与治疗
Minerva Med. 2003 Aug;94(4):201-14.

一氧化氮合酶3基因(NOS3)-T786C多态性与难治性高血压的关联:一项前瞻性队列研究。

Association between -T786C NOS3 polymorphism and resistant hypertension: a prospective cohort study.

作者信息

Cruz-González Ignacio, Corral Esther, Sánchez-Ledesma María, Sánchez-Rodríguez Angel, Martín-Luengo Cándido, González-Sarmiento Rogelio

机构信息

Cardiology Department, University Hospital of Salamanca, Salamanca, Spain.

出版信息

BMC Cardiovasc Disord. 2009 Aug 4;9:35. doi: 10.1186/1471-2261-9-35.

DOI:10.1186/1471-2261-9-35
PMID:19650939
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2734743/
Abstract

BACKGROUND

It is estimated that 5% of the hypertensive patients are resistant to conventional antihypertensive therapy. Polymorphisms in the endothelial nitric oxide synthase (NOS3) gene have been associated with high blood pressure levels, but not with resistant hypertension. The aim of the present study was to investigate if the -786T>C and G894T (Glu298Asp) polymorphisms of the NOS3 gene were associated with resistant hypertension.

METHODS

A prospective case-control observational study was performed. From a series of 950 consecutive patients followed up during 42 months, 48 patients with resistant hypertension were detected. 232 patients with controlled high blood pressure were also included.

RESULTS

No differences were observed in the distribution of G894T (Glu298Asp) NOS3 genotypes between the resistant hypertension group and the controlled hypertension patients. However, genotype -786CC was more frequent in the group of patients with resistant hypertension (33.3%) than in the group of patients with controlled high blood pressure (17.7%) (p 0.03). Furthermore carriers of allele T (-786TC and -786TT) were more frequent in patients with controlled hypertension (82.3%) than those with resistant hypertension (66.7%) (Multivariate analysis; RR 2.09; 95% CI 1.03-4.24; p 0.004).

CONCLUSION

Our results indicate that genotype -786CC of the NOS3 gene increase the susceptibility to suffer resistant hypertension, which suggest that resistance to conventional therapy could be determined at the endothelial level.

摘要

背景

据估计,5%的高血压患者对传统抗高血压治疗有抵抗性。内皮型一氧化氮合酶(NOS3)基因多态性与高血压水平相关,但与顽固性高血压无关。本研究的目的是调查NOS3基因的-786T>C和G894T(Glu298Asp)多态性是否与顽固性高血压相关。

方法

进行了一项前瞻性病例对照观察研究。在连续随访42个月的950例患者中,检测到48例顽固性高血压患者。还纳入了232例血压得到控制的高血压患者。

结果

在顽固性高血压组和血压得到控制的高血压患者之间,未观察到G894T(Glu298Asp)NOS3基因型分布的差异。然而,-786CC基因型在顽固性高血压患者组中(33.3%)比在血压得到控制的高血压患者组中(17.7%)更常见(p = 0.03)。此外,等位基因T(-786TC和-786TT)携带者在血压得到控制的高血压患者中(82.3%)比在顽固性高血压患者中(66.7%)更常见(多变量分析;RR = 2.09;95% CI 1.03 - 4.24;p = 0.004)。

结论

我们的结果表明,NOS3基因的-786CC基因型增加了患顽固性高血压的易感性,这表明对传统治疗的抵抗性可能在内皮水平上就已确定。