Dudley C, Keavney B, Casadei B, Conway J, Bird R, Ratcliffe P
Nuffield Department of Medicine, John Radcliffe Hospital, Headington, Oxford, UK.
J Hypertens. 1996 Feb;14(2):259-62. doi: 10.1097/00004872-199602000-00016.
To investigate whether the M235T polymorphism of the angiotensinogen (AGT) gene and the insertion/deletion (I/D) polymorphism of the angiotensin-1 converting enzyme (ACE) gene predict blood pressure response to different antihypertensive agents.
Sixty-three patients with untreated essential hypertension were randomly assigned in a placebo-controlled crossover comparison to atenolol 50 mg once daily, lisinopril 10 mg once daily and nifedipine SR 20 mg twice daily, and the effect on blood pressure was assessed by ambulatory blood pressure monitoring (ABPM). In a further 44 patients, placebo-controlled ABPM data were available after treatment with a single agent (atenolol 50 mg once daily in 16 cases and lisinopril 10mg once daily in 28 cases). The change in systolic and diastolic blood pressure achieved by each agent was analysed for association with genotypes at the AGT and ACE gene loci.
Polymerase chain reaction (PCR) amplification of genomic DNA from each individual was used to identify the I/D polymorphism of the ACE gene. The M235T polymorphism of the AGT gene was detected by Tth111I digestion of PCR product.
There was no significant association between response to any drug and either the AGT M235T or ACE I/D polymorphisms.
The large variability between individuals in the observed blood pressure response to these agents cannot be attributed to the polymorphisms analysed at the ACE and AGT loci.
研究血管紧张素原(AGT)基因的M235T多态性和血管紧张素转换酶(ACE)基因的插入/缺失(I/D)多态性是否能预测不同降压药物的血压反应。
63例未经治疗的原发性高血压患者被随机分配到安慰剂对照的交叉比较试验中,分别每日一次服用50mg阿替洛尔、每日一次服用10mg赖诺普利和每日两次服用20mg硝苯地平缓释片,并通过动态血压监测(ABPM)评估对血压的影响。另外44例患者在接受单一药物治疗(16例每日一次服用50mg阿替洛尔,28例每日一次服用10mg赖诺普利)后有安慰剂对照的ABPM数据。分析每种药物引起的收缩压和舒张压变化与AGT和ACE基因位点基因型的相关性。
采用聚合酶链反应(PCR)扩增每个个体的基因组DNA,以鉴定ACE基因的I/D多态性。通过对PCR产物进行Tth111I酶切检测AGT基因的M235T多态性。
对任何药物的反应与AGT M235T或ACE I/D多态性之间均无显著相关性。
个体对这些药物的血压反应差异较大,不能归因于ACE和AGT基因座分析的多态性。