• 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

因子V莱顿突变、亚甲基四氢叶酸还原酶及血管紧张素转换酶(插入/缺失)基因突变在成年高血压患者中的联合作用:一项来自土耳其锡瓦斯和恰纳卡莱的基于人群的研究

Combined effect of Factor V Leiden, MTHFR, and angiotensin-converting enzyme (insertion/deletion) gene mutations in hypertensive adult individuals: a population-based study from Sivas and Canakkale, Turkey.

作者信息

Demirel Yeltekin, Dogan Sezai, Uludag Ahmet, Silan Coskun, Atik Sinem, Silan Fatma, Ozdemir Ozturk

机构信息

Department of Family Medicine, Cumhuriyet University, Sivas, Turkey.

出版信息

Genet Test Mol Biomarkers. 2011 Nov;15(11):785-91. doi: 10.1089/gtmb.2011.0044. Epub 2011 Jun 23.

DOI:10.1089/gtmb.2011.0044
PMID:21699409
Abstract

BACKGROUND

Hypertension is one of the leading causes of mortality and morbidity in the world, which is influenced by environmental and genetic factors. The methylenetetrahydrofolate reductase (MTHFR) and angiotensin-converting enzymes (ACE) are possible candidate genes that may influence both body fatness and blood pressure (BP). The purpose of this study was to examine the carriage of gene combinations of the ACE (insertion/deletion [I/D]), MTHFR 677T and 1298C, and lipid profiles in patients with essential hypertension (EH) in Turkey.

METHODS

A total of 150 adult individuals (50 hypertensive, 50 first-degree relatives, and 50 healthy controls) from Sivas/Turkey with the same age and gender were assessed for body composition, lipid profiles, resting BP, and gene profiles. Additionally, 149 individuals (99 hypertensive, 50 controls) from Canakkale/Turkey had been investigated for ACE I/D polymorphism. Peripheral blood samples were genotyped using strip assay reverse-hybridization multiplex polymerase chain reaction tests for target genes.

RESULTS

Heterozygous mutation in FV Leiden was found to be higher in the hypertensive and first-degree relatives when compared with the control group (p<0.05). Homozygous DD alleles of the ACE gene were also higher than the ACE I/D and control groups (p<0.05). The high rates of cholesterol and low-density lipoprotein and low rates of high-density lipoprotein were found in patients with EH when compared with the control.

CONCLUSION

Results show that ACE with DD alleles and mutated alleles of FV Leiden and MTHFR genes were significantly different between genotypes and have a combined effect on EH in Turkish population. Further studies are needed to investigate the genetics of obesity, EH, and BP phenotypes in the current adult population.

摘要

背景

高血压是全球死亡和发病的主要原因之一,受环境和遗传因素影响。亚甲基四氢叶酸还原酶(MTHFR)和血管紧张素转换酶(ACE)是可能影响身体脂肪和血压(BP)的候选基因。本研究的目的是检测土耳其原发性高血压(EH)患者中ACE(插入/缺失[I/D])、MTHFR 677T和1298C基因组合的携带情况以及血脂谱。

方法

对来自土耳其锡瓦斯的150名年龄和性别相同的成年个体(50名高血压患者、50名一级亲属和50名健康对照)进行身体成分、血脂谱、静息血压和基因谱评估。此外,对来自土耳其恰纳卡莱的149名个体(99名高血压患者、50名对照)进行了ACE I/D多态性研究。使用针对目标基因的条带分析反向杂交多重聚合酶链反应试验对外周血样本进行基因分型。

结果

与对照组相比,高血压患者和一级亲属中FV Leiden杂合突变率更高(p<0.05)。ACE基因的纯合DD等位基因也高于ACE I/D组和对照组(p<0.05)。与对照组相比,EH患者中胆固醇和低密度脂蛋白水平高,高密度脂蛋白水平低。

结论

结果表明,在土耳其人群中,携带DD等位基因的ACE以及FV Leiden和MTHFR基因的突变等位基因在基因型之间存在显著差异,并且对EH有联合作用。需要进一步研究调查当前成年人群中肥胖、EH和BP表型的遗传学。

相似文献

1
Combined effect of Factor V Leiden, MTHFR, and angiotensin-converting enzyme (insertion/deletion) gene mutations in hypertensive adult individuals: a population-based study from Sivas and Canakkale, Turkey.因子V莱顿突变、亚甲基四氢叶酸还原酶及血管紧张素转换酶(插入/缺失)基因突变在成年高血压患者中的联合作用:一项来自土耳其锡瓦斯和恰纳卡莱的基于人群的研究
Genet Test Mol Biomarkers. 2011 Nov;15(11):785-91. doi: 10.1089/gtmb.2011.0044. Epub 2011 Jun 23.
2
Renin angiotensin system blockage associates with insertion/deletion polymorphism of angiotensin-converting enzyme in patients with hypertensive emergency.肾素血管紧张素系统阻断与高血压急症患者血管紧张素转换酶插入/缺失多态性相关。
DNA Cell Biol. 2013 Sep;32(9):541-8. doi: 10.1089/dna.2012.1951. Epub 2013 Jul 19.
3
Deletion polymorphism in the angiotensin-converting enzyme gene as a thrombophilic risk factor after hip arthroplasty.血管紧张素转换酶基因缺失多态性作为髋关节置换术后的血栓形成风险因素。
Thromb Haemost. 1998 Dec;80(6):869-73.
4
Methylenetetrahydrofolate reductase and angiotensin-converting enzyme gene polymorphisms among Saudi population from Qassim region.卡西姆地区沙特人群中亚甲基四氢叶酸还原酶和血管紧张素转换酶基因多态性
Genet Test Mol Biomarkers. 2009 Dec;13(6):817-20. doi: 10.1089/gtmb.2009.0019.
5
Thrombophilic gene polymorphisms and recurrent pregnancy loss in Greek women.希腊女性的血栓形成倾向基因多态性与复发性流产
Int J Lab Hematol. 2017 Dec;39(6):590-595. doi: 10.1111/ijlh.12703. Epub 2017 Jun 12.
6
The frequency of factor V Leiden and concomitance of factor V Leiden with prothrombin G20210A mutation and methylene tetrahydrofolate reductase C677T gene mutation in healthy population of Denizli, Aegean region of Turkey.土耳其爱琴海地区代尼兹利健康人群中因子V莱顿突变的频率,以及因子V莱顿与凝血酶原G20210A突变和亚甲基四氢叶酸还原酶C677T基因突变的共存情况。
Clin Appl Thromb Hemost. 2007 Apr;13(2):166-71. doi: 10.1177/1076029606298990.
7
Prevalence of thrombophilic mutations and ACE I/D polymorphism in Turkish ischemic stroke patients.土耳其缺血性中风患者中血栓形成倾向突变和ACE I/D多态性的患病率。
Clin Appl Thromb Hemost. 2009 Jul-Aug;15(4):415-20. doi: 10.1177/1076029608315163. Epub 2008 Apr 2.
8
Angiotensin-converting enzyme insertion/deletion polymorphism has no effect on the risk of atherosclerotic stroke or hypertension.血管紧张素转化酶插入/缺失多态性对动脉粥样硬化性卒中或高血压的发病风险无影响。
J Neurol Sci. 2009 Oct 15;285(1-2):137-41. doi: 10.1016/j.jns.2009.06.016.
9
A prospective case-control study analyzes 12 thrombophilic gene mutations in Turkish couples with recurrent pregnancy loss.一项前瞻性病例对照研究分析了土耳其复发性流产夫妇中 12 种血栓形成基因的突变。
Am J Reprod Immunol. 2010 Feb;63(2):126-36. doi: 10.1111/j.1600-0897.2009.00770.x. Epub 2009 Nov 10.
10
Interaction of MTHFR 1298C with ACE D allele augments the risk of diabetic nephropathy in Western Iran.MTHFR 1298C 与 ACE D 等位基因的相互作用增加了伊朗西部糖尿病肾病的风险。
DNA Cell Biol. 2012 Apr;31(4):553-9. doi: 10.1089/dna.2011.1364. Epub 2011 Sep 23.

引用本文的文献

1
Association Between Polymorphisms and the Risk of Essential Hypertension: An Updated Meta-analysis.多态性与原发性高血压风险之间的关联:一项更新的荟萃分析。
Front Genet. 2021 Nov 26;12:698590. doi: 10.3389/fgene.2021.698590. eCollection 2021.
2
Signaling pathway genes for blood pressure, folate and cholesterol levels among hypertensives: an epistasis analysis.高血压患者中血压、叶酸和胆固醇水平的信号通路基因:上位性分析
J Hum Hypertens. 2015 Feb;29(2):99-104. doi: 10.1038/jhh.2014.53. Epub 2014 Jul 24.
3
Associations of MTHFR gene polymorphisms with hypertension and hypertension in pregnancy: a meta-analysis from 114 studies with 15411 cases and 21970 controls.
亚甲基四氢叶酸还原酶基因多态性与高血压及妊娠高血压的相关性:来自 114 项研究的荟萃分析,包括 15411 例病例和 21970 例对照。
PLoS One. 2014 Feb 5;9(2):e87497. doi: 10.1371/journal.pone.0087497. eCollection 2014.
4
Association between polymorphism of MTHFR c.677C>T and risk of cardiovascular disease in Turkish population: a meta-analysis for 2.780 cases and 3.022 controls.MTHFR c.677C>T 多态性与土耳其人群心血管疾病风险的关联:2.780 例病例和 3.022 例对照的荟萃分析。
Mol Biol Rep. 2014 Jan;41(1):397-409. doi: 10.1007/s11033-013-2873-z. Epub 2013 Nov 22.
5
Top Three Pharmacogenomics and Personalized Medicine Applications at the Nexus of Renal Pathophysiology and Cardiovascular Medicine.肾脏病理生理学与心血管医学交叉领域的三大药物基因组学与个性化医学应用
Curr Pharmacogenomics Person Med. 2011 Dec;9(4):299-322. doi: 10.2174/187569211798377135.