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脯氨酰羧肽酶基因 E112D 多态性与中国高血压患者贝那普利降压反应的相关性。

E112D polymorphism in the prolylcarboxypeptidase gene is associated with blood pressure response to benazepril in Chinese hypertensive patients.

机构信息

Department of Cardiology, Peking University First Hospital, Beijing 100034, China.

出版信息

Chin Med J (Engl). 2009 Oct 20;122(20):2461-5.

Abstract

BACKGROUND

Marked interindividual variation exists in blood pressure response to benazepril, which is considered to have genetic basis. Our objectives were to evaluate whether the E112D polymorphism in the prolylcarboxypeptidase (PRCP) gene has impact on blood pressure response to benazepril.

METHODS

Hypertensive patients from Huoqiu County and Yuexi County of Anhui Province received daily treatment with an oral dosage of 10 mg benazepril for 15 days. Genotypes of the E112D polymorphism in the PRCP gene were determined by TaqMan SNP genotyping assay. Multivariate linear and Logistic regressions using generalized estimating equation model were performed in a total of 1092 patients to evaluate the association of PRCP genotypes and blood pressure response to benazepril.

RESULTS

Patients carrying ED or DD genotype had a less systolic blood pressure reduction (adjusted beta = -3.7 + or - 1.1, P < 0.001), a less diastolic blood pressure reduction (adjusted beta = -3.1 + or - 0.8, P < 0.001) and a lower percentage of reaching target blood pressure defined as SBP lower than 140 mmHg and DBP lower than 90 mmHg (adjusted OR = 0.6, P = 0.005) than those patients carrying EE genotype. In addition, the results from stratified analysis by county (Huoqiu or Yuexi) were similar to those observed in the pooled population.

CONCLUSIONS

Our data suggest that the E112D polymorphism in the PRCP gene may be a useful genetic marker to predict the antihypertensive effect of short-term benazepril treatment in hypertensive patients of Anhui Province, China.

摘要

背景

贝那普利的降压反应存在明显的个体间差异,这种差异被认为具有遗传基础。我们的目的是评估脯氨酰羧肽酶(PRCP)基因中的 E112D 多态性是否对贝那普利的降压反应有影响。

方法

来自安徽省霍邱县和岳西县的高血压患者每天接受 10 mg 贝那普利的口服治疗,共 15 天。采用 TaqMan SNP 基因分型检测法确定 PRCP 基因 E112D 多态性的基因型。采用广义估计方程模型的多变量线性和 Logistic 回归分析,共评估了 1092 例患者的 PRCP 基因型与贝那普利降压反应之间的关系。

结果

携带 ED 或 DD 基因型的患者收缩压降低幅度较小(校正β=-3.7+或-1.1,P<0.001),舒张压降低幅度较小(校正β=-3.1+或-0.8,P<0.001),血压达标率(定义为收缩压<140mmHg,舒张压<90mmHg)较低(校正 OR=0.6,P=0.005),而携带 EE 基因型的患者则较低。此外,按县(霍邱或岳西)分层分析的结果与汇总人群观察到的结果相似。

结论

我们的数据表明,PRCP 基因中的 E112D 多态性可能是预测中国安徽省高血压患者短期贝那普利降压治疗效果的有用遗传标记。

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