Yu Hui-Min, Lin Shu-Guang, Liu Guo-Zhang, Zhang Yu-Qing, Ma Wen-Jun, Deng Chun-Yu
Department of Cardiology, Guangdong Provincial People's Hospital and Guangdong Cardiovascular Institute, Guangzhou, China.
Clin Pharmacol Ther. 2006 Jun;79(6):581-9. doi: 10.1016/j.clpt.2006.02.007.
Our objective was to investigate the association between the -344C/T or A6547G polymorphism of the aldosterone synthase gene and the blood pressure response to angiotensin-converting enzyme inhibitors in a hypertensive cohort.
After a 2-week single-blind placebo run-in period, either benazepril or imidapril was administered for 6 weeks to 509 patients with mild to moderate essential hypertension. Polymerase chain reaction combined with restriction enzyme digestion was used to detect the 2 polymorphisms. The achieved changes in systolic and diastolic blood pressure were analyzed for their association with genotypes at the aldosterone synthase gene loci.
Regarding the -344C/T polymorphism, we observed the CC genotype in 53 patients (10.4%), the CT genotype in 204 (40.1%), and the TT genotype in 252 (49.5%). After 6 weeks of treatment, the reductions in diastolic blood pressure were significantly greater in patients carrying the TT or CT genotype compared with those carrying the CC genotype (9.1+/-7.0 mm Hg or 8.9+/-7.0 mm Hg versus 5.1+/-7.3 mm Hg, respectively; P=.001, ANOVA). Regarding the A6547G polymorphism, we observed the AA genotype in 19 patients (3.7%), the AG genotype in 184 (36.2%), and the GG genotype in 306 (60.1%). There were no significant differences in the blood pressure reductions after treatment among the 3 genotype groups, and there was no interaction between it and the -344C/T polymorphism. Stepwise multiple regression analysis showed that the significant predictors of diastolic blood pressure reduction at 6 weeks were baseline diastolic blood pressure (P<.001), -344C/T genotype (P=.007), and sex (P=.033).
The -344C/T variant, but not the A6547G variant, of the aldosterone synthase gene may be a determinant of the blood pressure response to angiotensin-converting enzyme inhibitors in hypertensive patients.
我们的目的是在一个高血压队列中研究醛固酮合成酶基因-344C/T或A6547G多态性与血压对血管紧张素转换酶抑制剂反应之间的关联。
经过2周的单盲安慰剂导入期后,对509例轻度至中度原发性高血压患者给予贝那普利或咪达普利治疗6周。采用聚合酶链反应联合限制性内切酶消化法检测这两种多态性。分析收缩压和舒张压的实际变化与醛固酮合成酶基因位点基因型之间的关联。
关于-344C/T多态性,我们观察到53例患者(10.4%)为CC基因型,204例(40.1%)为CT基因型,252例(49.5%)为TT基因型。治疗6周后,携带TT或CT基因型的患者舒张压降低幅度显著大于携带CC基因型的患者(分别为9.1±7.0 mmHg或8.9±7.0 mmHg对5.1±7.3 mmHg;P=0.001,方差分析)。关于A6547G多态性,我们观察到19例患者(3.7%)为AA基因型,184例(36.2%)为AG基因型,306例(60.1%)为GG基因型。3个基因型组治疗后血压降低幅度无显著差异,且与-344C/T多态性无相互作用。逐步多元回归分析显示,6周时舒张压降低的显著预测因素为基线舒张压(P<0.001)、-344C/T基因型(P=0.007)和性别(P=0.033)。
醛固酮合成酶基因的-344C/T变异而非A6547G变异可能是高血压患者血压对血管紧张素转换酶抑制剂反应的决定因素。