Suppr超能文献

血管紧张素原、血管紧张素II受体基因与血管紧张素转换酶抑制剂的血压反应之间的关联

Association between angiotensinogen, angiotensin II receptor genes, and blood pressure response to an angiotensin-converting enzyme inhibitor.

作者信息

Su Xiaowen, Lee Liming, Li Xiaohui, Lv Jun, Hu Yonghua, Zhan Siyan, Cao Weihua, Mei Ling, Tang Yong-Ming, Wang Dai, Krauss Ronald M, Taylor Kent D, Rotter Jerome I, Yang Huiying

机构信息

Medical Genetics Institute, Cedars-Sinai Medical Center, 8700 Beverly Blvd, Los Angeles, CA 90048, USA.

出版信息

Circulation. 2007 Feb 13;115(6):725-32. doi: 10.1161/CIRCULATIONAHA.106.642058. Epub 2007 Jan 29.

Abstract

BACKGROUND

To identify the genetic contribution to the variation in blood pressure (BP) response to angiotensin-converting enzyme inhibitors (ACEIs), single-nucleotide polymorphisms (SNPs) in the angiotensinogen (AGT), angiotensin receptor 1 (AGTR1), and angiotensin receptor 2 (AGTR2) genes were evaluated for their association with BP response to ACEI in Chinese patients with hypertension in a 2-stage design.

METHODS AND RESULTS

We selected 1447 hypertensive patients from a 3-year benazepril postmarket surveillance trial and genotyped them for 14 SNPs in the AGT, AGTR1, and AGTR2 genes. The AGT rs7079 (C/T) SNP (3'-untranslated region) was significantly associated with the response of diastolic BP to benazepril (diastolic BP response: -7.4 mm Hg for subjects with the CC genotype, -8.9 mm Hg for CA, and -10.1 mm Hg for AA; P=0.001). Although there was no association of individual SNPs in the AGTR1 gene, there was a graded response between common haplotypes and systolic BP reduction in the order of haplotype 2 (H2)/lack of haplotype 3 (non-H3) (-13.6 mm Hg) > non-H2/non-H3 (-10.9 mm Hg) > H3/non-H2 (-6.6 mm Hg) (P=0.004). The total variations in response to ACEI therapy that were explained by the AGT SNP and AGTR1 haplotype groups were 13% for systolic and 9% to 9.6% for diastolic BP, respectively.

CONCLUSIONS

AGT SNP rs7079 and AGTR1 haplotypes were associated with BP reduction in response to ACEI therapy in hypertensive Chinese patients. This will be useful in future studies, providing genetic markers to predict the hypertensive response to ACEI therapy.

摘要

背景

为了确定基因对血压(BP)对血管紧张素转换酶抑制剂(ACEI)反应差异的影响,采用两阶段设计,评估血管紧张素原(AGT)、血管紧张素受体1(AGTR1)和血管紧张素受体2(AGTR2)基因中的单核苷酸多态性(SNP)与中国高血压患者BP对ACEI反应的相关性。

方法与结果

我们从一项为期3年的贝那普利上市后监测试验中选取了1447例高血压患者,对其AGT、AGTR1和AGTR2基因中的14个SNP进行基因分型。AGT基因的rs7079(C/T)SNP(3'非翻译区)与舒张压对贝那普利的反应显著相关(舒张压反应:CC基因型受试者为-7.4 mmHg,CA基因型为-8.9 mmHg,AA基因型为-10.1 mmHg;P=0.001)。虽然AGTR1基因中的单个SNP无相关性,但常见单倍型与收缩压降低之间存在分级反应,顺序为单倍型2(H2)/缺乏单倍型3(非H3)(-13.6 mmHg)>非H2/非H3(-10.9 mmHg)>H3/非H2(-6.6 mmHg)(P=0.004)。AGT SNP和AGTR1单倍型组解释的ACEI治疗反应的总变异分别为收缩压的13%和舒张压的9%至9.6%。

结论

AGT SNP rs7079和AGTR1单倍型与中国高血压患者对ACEI治疗的血压降低相关。这将对未来的研究有用,为预测高血压患者对ACEI治疗的反应提供基因标记。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验