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肾素-血管紧张素系统基因多态性影响血压以及对血管紧张素转换酶抑制的反应。

Renin-angiotensin system gene polymorphisms influence blood pressure and the response to angiotensin converting enzyme inhibition.

作者信息

Hingorani A D, Jia H, Stevens P A, Hopper R, Dickerson J E, Brown M J

机构信息

Clinical Pharmacology Unit, University of Cambridge, UK.

出版信息

J Hypertens. 1995 Dec;13(12 Pt 2):1602-9.

PMID:8903618
Abstract

OBJECTIVES

To investigate the relationship between polymorphisms in the angiotensin converting enzyme (ACE), angiotensinogen (AGT) and type 1 angiotensin-II (AT1R) genes and (1) quantitative variations in blood pressure and (2) the blood pressure response to ACE inhibition in a hypertensive cohort.

DESIGN AND METHODS

We administered monotherapy with ACE inhibitors to 125 previously untreated essential hypertensives. Genotypes for ACE insertion and deletion, AGT M235T and AT1R A1166-->C polymorphisms were determined in DNA extracted from peripheral blood leucocytes. The influence of genotype on pretreatment blood pressure and the ACE inhibitor-induced decrease in blood pressure was tested by analysis of variance and multiple regression analysis, adjusting for age, sex, body mass index, alcohol intake and, where appropriate, pretreatment blood pressure.

RESULTS

ACE and AT1R genotypes were independent predictors of pretreatment systolic and diastolic blood pressure, with an apparent interaction between these two gene loci. Although it did not influence pretreatment blood pressure in this population, AGT genotype was an independent predictor of the blood pressure response to ACE inhibition.

CONCLUSIONS

The ACE and AT1R gene loci (chromosomes 17q and 3q, respectively) may carry alleles influencing blood pressure variation in this hypertensive population, with a possible epistatic interaction between the two loci. The AGT T235 allele does not appear to be a marker for blood pressure variation in this group, but variants on chromosome 1q lying in or near the AGT gene may contribute to individual differences in the blood pressure response to ACE inhibition. Among essential hypertensives, differences in the ACE inhibitor response appear, in part, to be genetically determined.

摘要

目的

在一个高血压队列中,研究血管紧张素转换酶(ACE)、血管紧张素原(AGT)和1型血管紧张素II受体(AT1R)基因多态性与(1)血压的定量变化以及(2)血压对ACE抑制的反应之间的关系。

设计与方法

我们对125名未经治疗的原发性高血压患者给予ACE抑制剂单一疗法。从外周血白细胞提取的DNA中确定ACE插入/缺失、AGT M235T和AT1R A1166→C多态性的基因型。通过方差分析和多元回归分析,在调整年龄、性别、体重指数、酒精摄入量以及适当情况下的治疗前血压后,测试基因型对治疗前血压和ACE抑制剂引起的血压降低的影响。

结果

ACE和AT1R基因型是治疗前收缩压和舒张压的独立预测因子,这两个基因位点之间存在明显的相互作用。虽然AGT基因型在该人群中不影响治疗前血压,但它是血压对ACE抑制反应的独立预测因子。

结论

ACE和AT1R基因位点(分别位于17号染色体q和3号染色体q)可能携带影响该高血压人群血压变化的等位基因,两个位点之间可能存在上位性相互作用。AGT T235等位基因似乎不是该组血压变化的标志物,但位于AGT基因内或附近的1号染色体上的变异可能导致血压对ACE抑制反应的个体差异。在原发性高血压患者中,ACE抑制剂反应的差异部分似乎是由基因决定的。

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