ace(I/D)基因多态性Ⅰ/Ⅱ期高血压患者应用降压药的疗效

Bansal G, Chaithanya Tm, Al-Aaly Ma, Manchi Rk
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引用次数: 0

摘要

背景:血管紧张素转换酶(ACE)是调节血压的关键酶,它由位于17号染色体上的由26个外显子组成的21kb基因编码,具有插入(I)或缺失(D)形式的多态性。目的是研究降压药对ACE基因多态性相关的原发性高血压患者的疗效。方法:招募高血压患者,进行ACE基因多态性基因检测,将患者分为A组和B组。A和B组分别给予阿替洛尔(25mg)和阿齐沙坦(40mg)治疗3个月。结果:两组患者在开始治疗前后均记录了收缩压和舒张压。在88例新诊断的高血压患者中,大多数研究人群属于基因型D/D(38.63%),其次是I/D(31.81%)和II(29.54%)。结论:无论治疗组与对照组相比,I/I基因型血压控制率均较高,D/D基因型次之。在ACE基因多态性患者中,观察到40mg阿齐沙坦与25mg阿替洛尔治疗的总体预后更好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effectiveness of antihypertensive agents in stage I/II hypertensive patients with ace (I/D) gene polymorphism
Background: Angiotensin converting enzyme (ACE) is the key enzyme, regulates the blood pressure which is encoded by 21kb gene that consists of 26 exons and is located on chromosome 17, contains a polymorphism in the form of either Insertion (I) or Deletion (D). The aim was to study the effect of antihypertensive drugs in patients of essential hypertension associated with ACE gene polymorphism. Methods: Hypertensive patients were recruited followed by genetic test was done for detecting ACE gene polymorphism, then patients were divided as Group-A & B. Group –A and B patients were treated with atenolol (25mg) and azilsartan (40 mg) for three months respectively. Results: Systolic and diastolic blood pressure was recorded in both the groups before and after commencement of treatment. Among 88 patients of newly diagnosed hypertension, majority of study population belongs to genotype D/D (38.63%) followed by I/D (31.81%) and II (29.54%) genotype. Significant difference was found in systolic blood pressure (p<0.05) of both groups but not diastolic blood pressure (p>0.05). Conclusion: The rate of control of blood pressure was high in I/I genotype followed by D/D genotype irrespective of treatment group. Overall better prognosis was observed with azilsartan 40mg compared to atenolol 25mg treatment in patients with ACE gene polymorphisms.
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