• 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 the M235T polymorphism of the AGT gene and cytokines in patients with hypertension.高血压患者AGT基因M235T多态性与细胞因子之间的关联
Exp Ther Med. 2012 Mar;3(3):509-512. doi: 10.3892/etm.2011.433. Epub 2011 Dec 23.
2
[Studies of the association between angiotensinogen gene regulation and cytokines in essential hypertension].[原发性高血压中血管紧张素原基因调控与细胞因子之间关联的研究]
Yi Chuan Xue Bao. 2003 Oct;30(10):978-82.
3
Association of angiotensinogen M235T and A(-6)G gene polymorphisms with coronary heart disease with independence of essential hypertension: the PROCAGENE study. Prospective Cardiac Gene.血管紧张素原M235T和A(-6)G基因多态性与冠心病的关联及与原发性高血压的独立性:PROCAGENE研究。前瞻性心脏基因研究
J Am Coll Cardiol. 2001 May;37(6):1536-42. doi: 10.1016/s0735-1097(01)01186-x.
4
Genetic background of left ventricular hypertrophy in Uzbek hypertensive men.乌兹别克斯坦高血压男性左心室肥厚的遗传背景
Turk Kardiyol Dern Ars. 2010 Oct;38(7):466-72.
5
[Association of angiotensinogen gene M235T variant with essential hypertension].血管紧张素原基因M235T变异与原发性高血压的关联
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2004 Mar;33(2):151-4. doi: 10.3785/j.issn.1008-9292.2004.02.014.
6
Association between molecular variants of the angiotensinogen gene and hypertension in Amis tribes of eastern Taiwan.台湾东部阿美族人群中血管紧张素原基因分子变异与高血压的关联。
J Formos Med Assoc. 2002 Mar;101(3):183-8.
7
Gender-related association of AGT gene variants (M235T and T174M) with essential hypertension--a case-control study.AGT 基因变异(M235T 和 T174M)与原发性高血压的性别相关性——一项病例对照研究。
Clin Exp Hypertens. 2012;34(1):38-44. doi: 10.3109/10641963.2011.618207. Epub 2011 Dec 9.
8
[A molecular variant of angiotensinogen gene is associated with myocardial infarction in Chinese].血管紧张素原基因的一种分子变体与中国人群的心肌梗死相关
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 1998 Jun 10;15(3):133-5.
9
The Association of M235T Genetic Polymorphism in Gene and Other Non-Genetic Factors with Essential Hypertension among Jordanian Patients.约旦患者中基因M235T遗传多态性及其他非遗传因素与原发性高血压的关联
J Pers Med. 2024 Feb 29;14(3):273. doi: 10.3390/jpm14030273.
10
Association between renin-angiotensin-aldosterone system genotypes and haplotypes and risk of ischemic stroke of atherosclerotic etiology.肾素-血管紧张素-醛固酮系统基因与单倍型和动脉粥样硬化性病因缺血性卒中风险之间的关联。
Acta Neurol Scand. 2009 Jun;119(6):356-63. doi: 10.1111/j.1600-0404.2008.01105.x.

引用本文的文献

1
Genetic Variations Related to Angiotensin II Production and Risk for Basal Cell Carcinoma.与血管紧张素II生成及基底细胞癌风险相关的基因变异
Biochem Genet. 2025 Apr;63(2):917-935. doi: 10.1007/s10528-024-10746-0. Epub 2024 Mar 28.
2
Influence of blood pressure polygenic risk scores and environmental factors on coronary artery disease in the Korean Genome and Epidemiology Study.韩国基因组与流行病学研究中血压多基因风险评分及环境因素对冠状动脉疾病的影响
J Hum Hypertens. 2024 Mar;38(3):221-227. doi: 10.1038/s41371-023-00878-y. Epub 2023 Nov 20.
3
Implication of therapeutic outcomes associated with molecular characterization of paediatric aplastic anaemia.小儿再生障碍性贫血分子特征与治疗结果的关联
Biochem Biophys Rep. 2021 Jan 9;25:100899. doi: 10.1016/j.bbrep.2020.100899. eCollection 2021 Mar.
4
Genetic factors contributing to hypertension in African-based populations: A systematic review and meta-analysis.遗传因素与非洲人群高血压的相关性:系统评价和荟萃分析。
J Clin Hypertens (Greenwich). 2018 Mar;20(3):485-495. doi: 10.1111/jch.13225. Epub 2018 Mar 9.
5
Gender specific association of RAS gene polymorphism with essential hypertension: a case-control study.RAS 基因多态性与原发性高血压的性别相关性:病例对照研究。
Biomed Res Int. 2014;2014:538053. doi: 10.1155/2014/538053. Epub 2014 Apr 17.
6
Genetic and Adverse Health Outcome Associations with Treatment Resistant Hypertension in GenHAT.GenHAT研究中与难治性高血压相关的遗传因素及不良健康结局关联
Int J Hypertens. 2013;2013:578578. doi: 10.1155/2013/578578. Epub 2013 Oct 31.

本文引用的文献

1
Mutation of V896M in cardiac myosin binding protein-c gene in two Chinese families with hypertrophic cardiomyopathy.
Mol Med Rep. 2010 Sep-Oct;3(5):759-63. doi: 10.3892/mmr.2010.333. Epub 2010 Jul 20.
2
Linkage of angiotensinogen gene polymorphisms with hypertension in a sibling study of Hong Kong Chinese.血管紧张素原基因多态性与香港华人同胞兄弟研究中高血压的连锁
J Hypertens. 2010 Jun;28(6):1203-9. doi: 10.1097/HJH.0b013e3283384b07.
3
Association of angiotensinogen gene M235T and angiotensin-converting enzyme gene I/D polymorphisms with essential hypertension in Han Chinese population: a meta-analysis.血管紧张素原基因 M235T 和血管紧张素转换酶基因 I/D 多态性与汉族人群原发性高血压的相关性:荟萃分析。
J Hypertens. 2010 Mar;28(3):419-28. doi: 10.1097/HJH.0b013e32833456b9.
4
Angiotensinogen T174M and M235T variants and hypertension in the Hani and Yi minority groups of China.中国哈尼族和彝族人群中血管紧张素原T174M和M235T变异与高血压的关系
Biochem Genet. 2009 Jun;47(5-6):344-50. doi: 10.1007/s10528-009-9237-3. Epub 2009 Apr 14.
5
M235T polymorphism of the angiotensinogen gene and insertion/deletion polymorphism of the angiotensin-1 converting enzyme gene in essential arterial hypertension in Caucasians.高加索人群原发性高血压中血管紧张素原基因的M235T多态性与血管紧张素转换酶基因的插入/缺失多态性
Folia Biol (Praha). 2007;53(2):69-70.
6
Mistyping of angiotensinogen M235T alleles.
Hypertens Res. 2006 Mar;29(3):197-201. doi: 10.1291/hypres.29.197.
7
Association of angiotensinogen gene polymorphisms with essential hypertension in African-Americans and Caucasians.非洲裔美国人和高加索人中血管紧张素原基因多态性与原发性高血压的关联。
Hum Hered. 2005;60(2):89-96. doi: 10.1159/000088657. Epub 2005 Oct 4.
8
Three single-nucleotide polymorphisms of the angiotensinogen gene and susceptibility to hypertension: single locus genotype vs. haplotype analysis.血管紧张素原基因的三个单核苷酸多态性与高血压易感性:单基因座基因型与单倍型分析
Physiol Genomics. 2004 Apr 13;17(2):79-86. doi: 10.1152/physiolgenomics.00133.2003.
9
Angiotensinogen gene promoter region variant modifies body size-ambulatory blood pressure relations in hypertension.血管紧张素原基因启动子区域变异改变高血压患者体型与动态血压的关系。
Circulation. 2002 Sep 17;106(12):1483-7. doi: 10.1161/01.cir.0000029093.93362.fc.
10
Angiotensin-related genes involved in essential hypertension: allelic distribution in an Italian population sample.
Ital Heart J. 2001 Aug;2(8):589-93.

高血压患者AGT基因M235T多态性与细胞因子之间的关联

Association between the M235T polymorphism of the AGT gene and cytokines in patients with hypertension.

作者信息

Cheng Jing-Lin, Wang Ai-Ling, Wan Jun

机构信息

Department of Emergency, Second Affiliated Hospital of Anhui Medical University, Hefei 230601;

出版信息

Exp Ther Med. 2012 Mar;3(3):509-512. doi: 10.3892/etm.2011.433. Epub 2011 Dec 23.

DOI:10.3892/etm.2011.433
PMID:22969920
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3438648/
Abstract

The aim of the present study was to explore the association between the M235T polymorphism of the angiotensinogen (AGT) gene and cytokines in patients with essential hypertension (EH). A total of 300 patients with EH and an age-matched control group of 150 individuals without EH, secondary hypertension, myocardial infarction and diabetes were enrolled in this study. Polymerase chain reaction combined with restriction fragment length polymorphism (PCR-RFLP) was used to detect variation in the target genotype, and enzyme-linked immunosorbant assay (ELISA) was used to detect the cytokine [interleukin (IL)-1, IL-6 and tumor necrosis factor-α (TNF-α)] concentrations. The AGT gene 235T allele and 235TT genotype frequencies in hypertensive patients were slightly higher than those in the controls. Furthermore, in the hypertensive subjects with the AGT gene 235T allele, the concentrations of IL-1 and TNF-α were significant higher than those in the controls. The results from our study suggest that the higher AGT gene TT genotype and 235T allele frequencies may be risk factors for hypertension. High frequencies of the AGT gene 235T allele and high cytokine concentrations (IL-1 and TNF-α) may promote the transcription and expression of AGT, particularly in hypertensive patients with the 235TT genotype.

摘要

本研究的目的是探讨原发性高血压(EH)患者血管紧张素原(AGT)基因M235T多态性与细胞因子之间的关联。本研究共纳入300例EH患者以及150例年龄匹配的对照个体,这些对照个体无EH、继发性高血压、心肌梗死和糖尿病。采用聚合酶链反应联合限制性片段长度多态性(PCR-RFLP)检测目标基因型的变异,并采用酶联免疫吸附测定(ELISA)检测细胞因子[白细胞介素(IL)-1、IL-6和肿瘤坏死因子-α(TNF-α)]浓度。高血压患者中AGT基因235T等位基因和235TT基因型频率略高于对照组。此外,在携带AGT基因235T等位基因的高血压受试者中,IL-1和TNF-α的浓度显著高于对照组。我们的研究结果表明,较高的AGT基因TT基因型和235T等位基因频率可能是高血压的危险因素。AGT基因235T等位基因的高频率和高细胞因子浓度(IL-1和TNF-α)可能促进AGT的转录和表达,尤其是在携带235TT基因型的高血压患者中。