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1
ACE and AT1R gene polymorphisms and hypertension in Indian population.印度人群中血管紧张素转换酶(ACE)和血管紧张素Ⅱ1型受体(AT1R)基因多态性与高血压
J Clin Lab Anal. 2000;14(5):230-7. doi: 10.1002/1098-2825(2000)14:5<230::AID-JCLA6>3.0.CO;2-U.
2
Identification of two LDL-receptor mutations causing familial hypercholesterolemia in Indian subjects by a simplified rapid PCR-heteroduplex method.通过简化快速PCR-异源双链法鉴定印度受试者中导致家族性高胆固醇血症的两种低密度脂蛋白受体突变。
Clin Chem. 2000 Aug;46(8 Pt 1):1183-5.
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The san diego conference nucleic acid technologies in disease detection november 17-19, 1999.
Clin Chem. 1999 Nov;45(11):2047-53.
4
1166 A/C polymorphism of the angiotensin II type 1 receptor gene and the response to short-term infusion of angiotensin II.血管紧张素II 1型受体基因的1166 A/C多态性与对血管紧张素II短期输注的反应
Circulation. 1999 Sep 28;100(13):1394-9. doi: 10.1161/01.cir.100.13.1394.
5
Angiotensinogen M235T polymorphism is associated with plasma angiotensinogen and cardiovascular disease.血管紧张素原M235T基因多态性与血浆血管紧张素原及心血管疾病相关。
Am Heart J. 1999 Apr;137(4 Pt 1):698-705. doi: 10.1016/s0002-8703(99)70226-7.
6
Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertension.1型血管紧张素II受体基因座参与原发性高血压的证据。
Hypertension. 1999 Mar;33(3):844-9. doi: 10.1161/01.hyp.33.3.844.
7
Angiotensin-converting enzyme and angiotensin II receptor 1 polymorphisms: association with early coronary disease.血管紧张素转换酶和血管紧张素II受体1基因多态性:与早期冠心病的关联。
Cardiovasc Res. 1998 Nov;40(2):375-9. doi: 10.1016/s0008-6363(98)00179-5.
8
Angiotensin II type 1 receptor A1166C gene polymorphism. Absence of an association with the risk of coronary artery disease and myocardial infarction and of a synergistic effect with angiotensin-converting enzyme gene polymorphism on the risk of these diseases.血管紧张素II 1型受体A1166C基因多态性。与冠状动脉疾病和心肌梗死风险无关联,且与血管紧张素转换酶基因多态性在这些疾病风险上无协同作用。
Eur Heart J. 1998 Nov;19(11):1657-65. doi: 10.1053/euhj.1998.1097.
9
Angiotensin converting enzyme gene polymorphism in coronary artery disease: the Indian scenario.
Clin Chem Lab Med. 1998 Aug;36(8):621-4. doi: 10.1515/CCLM.1998.108.
10
Is the A1166C polymorphism of the angiotensin II type 1 receptor involved in cardiovascular disease?血管紧张素II 1型受体的A1166C多态性与心血管疾病有关吗?
Eur Heart J. 1998 Jul;19 Suppl G:G13-7.

肾素血管紧张素系统基因与冠心病

Genes of renin angiotensin system and coronary heart disease.

作者信息

Ashavaid T F, Shalia K K, Nair K G, Dalal J J

机构信息

Research Laboratories, P.D. Hinduja National Hospital & Medical Research Centre, Veer Savarkar Marg, Mahim, 400 016 Mumbai.

出版信息

Indian J Clin Biochem. 2000 Aug;15(Suppl 1):1-10. doi: 10.1007/BF02867539.

DOI:10.1007/BF02867539
PMID:23105263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3454074/
Abstract

Coronary constriction, proliferation of smooth muscle cells and arrhythmia are involved in the pathophysiology of coronary heart disease and its complications such as myocardial infarction and sudden death. All these effects are favoured by high angiotensin II levels. Angiotensin II is the main effector molecule of the renin angiotensin system and it acts through angiotensin II type receptors. Genetically determined differences in the expression of the components of this system could adversely affect angiotensin II concentration and subsequently heart. Consequently each component of this system represents a potential candidate in the etiology of cardiovascular disease. In this article we review the variation of the angiotensin I converting enzyme, angiotensin II type I receptor and angiotensinogen genes and their association with cardiovascular disease.

摘要

冠状动脉收缩、平滑肌细胞增殖和心律失常参与了冠心病及其并发症(如心肌梗死和猝死)的病理生理过程。所有这些效应都受到高血管紧张素II水平的促进。血管紧张素II是肾素血管紧张素系统的主要效应分子,它通过血管紧张素II 1型受体发挥作用。该系统各组分表达的遗传决定差异可能会对血管紧张素II浓度产生不利影响,进而影响心脏。因此,该系统的每个组分都是心血管疾病病因学中的潜在候选因素。在本文中,我们综述了血管紧张素I转换酶、血管紧张素II 1型受体和血管紧张素原基因的变异及其与心血管疾病的关联。