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血管紧张素I转换酶和血管紧张素II 1型受体基因变异之间的上位性相互作用与冠状动脉粥样硬化程度的关系

Epistatic interaction between variations in the angiotensin I converting enzyme and angiotensin II type 1 receptor genes in relation to extent of coronary atherosclerosis.

作者信息

Ye S, Dhillon S, Seear R, Dunleavey L, Day L B, Bannister W, Day I N M, Simpson I

机构信息

Human Genetics Division, University of Southampton School of Medicine, Southampton General Hospital, Southampton, UK.

出版信息

Heart. 2003 Oct;89(10):1195-9. doi: 10.1136/heart.89.10.1195.

Abstract

OBJECTIVE

To test the hypothesis that gene-gene interaction of the renin-angiotensin system is associated with an effect on the extent of coronary atherosclerosis.

SETTING AND RESULTS

A cohort of 1162 patients with coronary artery disease were genotyped for genetic polymorphisms in the renin-angiotensin system. Patients carrying the D allele of the angiotensin I converting enzyme (ACE) gene had greater coronary extent scores (defined as the number of coronary segments with 5% to 75% stenosis) than those not carrying this allele (p = 0.006 in non-parametric analysis and p = 0.019 in parametric analysis). This association remained significant after adjusting for age, body mass index, hypertension, and diabetes, which were also significantly associated with coronary extent scores. There was a significant interaction (p = 0.033) between genotypes of ACE and angiotensin II type 1 receptor (AGTR1). The association between the ACE gene D allele and increased coronary extent scores was significant (p = 0.008 in non-parametric and p = 0.027 in parametric analysis) in those carrying the +1166 C allele of the AGTR1 gene, but was absent in those not carrying the AGTR1 gene +1166 C allele.

CONCLUSION

These findings suggest that variation in the ACE and AGTR1 genes and their interaction may not only contribute to susceptibility of coronary artery disease as previously found but also modify the disease process, thus contributing to interindividual differences in severity of the disease.

摘要

目的

检验肾素 - 血管紧张素系统的基因 - 基因相互作用与冠状动脉粥样硬化程度相关的假说。

设置与结果

对1162例冠心病患者进行肾素 - 血管紧张素系统基因多态性基因分型。携带血管紧张素I转换酶(ACE)基因D等位基因的患者比未携带该等位基因的患者有更高的冠状动脉病变程度评分(定义为狭窄程度在5%至75%的冠状动脉节段数)(非参数分析中p = 0.006,参数分析中p = 0.019)。在对年龄、体重指数、高血压和糖尿病进行校正后,这种关联仍然显著,而这些因素也与冠状动脉病变程度评分显著相关。ACE基因和血管紧张素II 1型受体(AGTR1)的基因型之间存在显著的相互作用(p = 0.033)。在携带AGTR1基因+1166 C等位基因的患者中,ACE基因D等位基因与冠状动脉病变程度评分增加之间的关联显著(非参数分析中p = 0.008,参数分析中p = 0.027),而在未携带AGTR1基因+1166 C等位基因的患者中则不存在这种关联。

结论

这些发现表明,ACE和AGTR1基因的变异及其相互作用不仅可能如先前发现的那样导致冠心病易感性增加,还可能改变疾病进程,从而导致个体间疾病严重程度的差异。

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