Molecular Cardiology Lab, Dr. B.R. Ambedkar Centre for Biomedical Research, University of Delhi, India.
J Pharm Pharm Sci. 2012;15(3):399-406. doi: 10.18433/j3kw3b.
It has been suggested that genetic backgrounds, which have an association with essential hypertension, may also determine the responsiveness to ACE inhibitor. We determined the association of angiotensinogen (M235T) gene polymorphism with essential hypertension and the relationship between polymorphism in the angiotensinogen (M235T) gene and blood pressure response to ACE inhibitor (Enalapril) in patients with essential hypertension from northern Indian subjects.
250 patients with essential hypertension and 250 normal healthy controls from Delhi and surrounding areas were recruited for the investigation. Blood pressure was recorded before and after 6 weeks of treatment with ACE inhibitors, Enalapril. Genotyping were carried out by polymerase chain reaction and Restriction fragment length polymorphism technique.
Statistically significant association of T allele was observed with essential hypertension [x2 = 14.67, p = 0.00013, Odds ratio = 1.76 (1.3-2.32) at 95% CI], the relative risk at 95% CI being 1.28 (1.2-1.54). The decrease in systolic blood pressure and diastolic blood pressure after six weeks of treatment of the patients carrying TT genotype (SBP = 26 ± 17.4 mmHg, DBP = 14.83 ± 7.6 mmHg) were greater than the groups carrying MT (SBP = 3.0 ± 7.8 mmHg, DBP = 6.2 ± 3.0 mmHg) and MM genotypes (SBP = 1.2 ± 0.8 mmHg, DBP = 0.10 ± 12.1 mm Hg.
The angiotensinogen (M235T) gene polymorphism is significantly associated with essential hypertension. Patients carrying TT genotype had higher blood pressure lowering response when treated with ACE inhibitor, Enalapril than those carrying MM and MT genotypes suggesting that the T allele may be a possible genetic marker for essential hypertension.
有人认为,与原发性高血压相关的遗传背景也可能决定血管紧张素转换酶抑制剂(ACEI)的反应性。我们旨在确定血管紧张素原(M235T)基因多态性与原发性高血压的相关性,以及血管紧张素原(M235T)基因多态性与来自印度北部地区的原发性高血压患者对 ACEI(依那普利)的血压反应之间的关系。
从德里及周边地区招募了 250 名原发性高血压患者和 250 名健康对照者进行这项研究。在开始 ACEI 依那普利治疗前和治疗 6 周后记录血压。通过聚合酶链反应和限制性片段长度多态性技术进行基因分型。
TT 等位基因与原发性高血压存在显著相关性[x2 = 14.67,p = 0.00013,优势比(OR)= 1.76(1.3-2.32),95%置信区间(CI)],95%CI 中的相对风险为 1.28(1.2-1.54)。携带 TT 基因型的患者在接受治疗 6 周后收缩压和舒张压的降低幅度(SBP = 26 ± 17.4mmHg,DBP = 14.83 ± 7.6mmHg)大于携带 MT 基因型(SBP = 3.0 ± 7.8mmHg,DBP = 6.2 ± 3.0mmHg)和 MM 基因型(SBP = 1.2 ± 0.8mmHg,DBP = 0.10 ± 12.1mmHg)的患者。
血管紧张素原(M235T)基因多态性与原发性高血压显著相关。携带 TT 基因型的患者在接受 ACEI 依那普利治疗时血压降低反应更高,而携带 MM 和 MT 基因型的患者则较低,这表明 T 等位基因可能是原发性高血压的一个潜在遗传标志物。