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血管紧张素1转换酶编码基因多态性及其与脑梗死中翻译后产物的关系。

Polymorphisms in the gene encoding angiotensin 1-converting enzyme and relationship to its post-translational product in cerebral infarction.

作者信息

Sharma P, Carter N D, Barley J, Lunt R, Seymour C A, Brown M M

机构信息

Division of Clinical Neuroscience, St. George's Hospital Medical School, London, UK.

出版信息

J Hum Hypertens. 1994 Aug;8(8):633-4.

PMID:7990099
Abstract

There is increasing evidence to suggest that the gene encoding angiotensin 1-converting enzyme (ACE) plays a significant part in cardiac disease risk. It is not clear if this risk is due to atherosclerotic factors in general or whether its influence is local to cardiac tissue. Previous studies have suggested that there is a genetic control of plasma ACE levels in normal subjects. We sought to see if such a relationship also existed amongst computer tomography (CT) proven cerebral infarction. Twenty-eight patients with stroke and 19 control subjects were grouped according to their ACE genotype and their plasma ACE levels were assessed. Although there is a trend for plasma levels to be associated with the variant ACE alleles there was a wide overlap. However, when compared with their respective alleles in control subjects there was no difference. We conclude that any future evaluation of stroke risk from the ACE gene will need to determine both plasma ACE level and genotype.

摘要

越来越多的证据表明,编码血管紧张素1转换酶(ACE)的基因在心脏病风险中起着重要作用。目前尚不清楚这种风险是总体上归因于动脉粥样硬化因素,还是其影响仅限于心脏组织局部。先前的研究表明,正常受试者的血浆ACE水平存在遗传控制。我们试图探究在计算机断层扫描(CT)证实的脑梗死患者中是否也存在这种关系。28例中风患者和19名对照受试者根据其ACE基因型进行分组,并评估其血浆ACE水平。尽管血浆水平有与ACE变异等位基因相关的趋势,但存在广泛的重叠。然而,与对照受试者各自的等位基因相比,没有差异。我们得出结论,未来任何基于ACE基因对中风风险的评估都需要同时测定血浆ACE水平和基因型。

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