Association of angiotensin converting enzyme gene polymorphism with diabetic nephropathy in patients using lisinopril

Hammad Ullah, A. Razaq, S. Altaf, T. Basharat, S. Tariq, Sami Siraj, A. Azhar, Waheed lqbal, Haroon Khan
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Abstract

Angiotensin Converting Enzyme (ACE) plays an important role in the development and progression of Diabetic nephropathy (DN). The present study was designed to determine the possible association between ACE gene polymorphism and DN. The study included 242 samples: DN (n = 121), type 2 Diabetes mellitus (DM2) (n = 60) and control (n = 61). The blood samples were collected from the subjects, followed by DNA extraction. Insertion deletion polymorphism of ACE gene studied using specific primers. Patients using Lisinopril were followed for two months. The ACE genotype distribution in DN patients was as follows: DD (n = 47; 38.84%), II (n = 17; 14.04%) and DI (n = 57; 47.10%). In DM group the genotype distribution was DD (n = 4; 6.66%), II (n = 25; 41.66%) and DI (n = 31; 51.66%) while in control group DD (n = 38; 62.29%), II (n = 1; 1.63%) and DI (n = 22; 36.06%). The comparison of II genotype to DD genotype was reflected by p-value =0.0001, OR=17.28 and 95% CI 5.313-49.58. The percent decrease of micro-albuminuria after two months with the use of Lisinopril 10 mg twice a day in DD, II and DI genotype of DN were 31.27%, 12.37% and 16.81%, respectively. Our findings revealed that DD genotype has strong association with DN but not a risk factor for development of disease.
血管紧张素转换酶基因多态性与赖诺普利患者糖尿病肾病的关系
血管紧张素转换酶(ACE)在糖尿病肾病(DN)的发生发展中起重要作用。本研究旨在确定ACE基因多态性与DN之间可能的关联。研究共纳入242例样本:DN (n = 121)、2型糖尿病(DM2) (n = 60)和对照组(n = 61)。从受试者身上采集血液样本,然后提取DNA。利用特异性引物研究ACE基因的插入缺失多态性。使用赖诺普利的患者随访2个月。肾病患者ACE基因型分布如下:DD (n = 47;38.84%), II (n = 17;14.04%)和DI (n = 57;47.10%)。DM组基因型分布为DD (n = 4;6.66%), II (n = 25;41.66%)和DI (n = 31;51.66%),对照组DD (n = 38;62.29%), II (n = 1;1.63%)和DI (n = 22;36.06%)。II基因型与DD基因型比较,p值=0.0001,OR=17.28, 95% CI为5.313 ~ 49.58。赖诺普利10 mg / d 2次用药2个月后,DD、II和DI基因型DN患者微量蛋白尿下降率分别为31.27%、12.37%和16.81%。我们的研究结果表明,DD基因型与DN有很强的相关性,但不是疾病发展的危险因素。
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