Nakhjavani Manouchehr, Esfahanian Fatemeh, Jahanshahi Alireza, Esteghamati Alireza, Nikzamir Abdol Rahim, Rashidi Armin, Zahraei Mahin
Endocrine and Metabolism Research Center, Vali-Asr Hospital, and Department of Biochemistry, School of Medicine, Medical Sciences, University of Tehran, No 12, Aramesh Alley, Mellat Park, Tehran, Iran.
Nephrol Dial Transplant. 2007 Sep;22(9):2549-53. doi: 10.1093/ndt/gfm252. Epub 2007 May 3.
Observations on the association between the ACE gene polymorphism and hypertension have been inconsistent, which might be due to ethnic and geographical variations. Moreover, the relationship between insertion/deletion (I/D) polymorphism and hypertension in the diabetic population has not been sufficiently studied. The aim of this study was to evaluate for the first time the possible association between I/D polymorphism and hypertension in an Iranian diabetic adult population.
A total of 82 consecutive patients with type 2 diabetes and hypertension (Group A) and 87 patients with type 2 diabetes but without hypertension (Group B) were included. Patients who had a history of hypertension before the onset of diabetes and those with findings suggesting secondary hypertension were excluded. The following variables were determined for each patient: age, sex, body mass index (BMI), diabetes duration and the drugs used, history of coronary artery disease and its complications, blood pressure (systolic and diastolic), fasting blood sugar (FBS), haemoglobin A1c (HbA1c), total cholesterol (Chol), low-density lipoproteins (LDL), high-density lipoproteins (HDL), triglycerides (TG), plasma creatinine (Crt) and 24 h urine albumin excretion. Polymerase chain reaction (PCR) was used to detect the I/D alleles. Univariate (chi-squared and t-test) and multivariate (multivariate binary logistic regression with adjusted odds ratios) analyses were applied to determine the association between I/D polymorphism (with genotype II as reference) and hypertension. P<0.05 was considered statistically significant.
In univariate analysis, the groups were statistically similar in all variables except for diabetes duration (156.05+/-73.54 months in Group A vs 121.74+/-65.53 months in Group B; P=0.002), Crt (1.04+/-0.25 mg/dl in Group A vs 0.93+/-0.23 mg/dl in Group B; P=0.003), albuminuria (486.25+/-484.60 mg/d in Group A vs 316.50+/-459.56 mg/d in Group B; P=0.021) and the frequency of DD genotype (27 cases in Group A vs 11 cases in Group B; P=0.026). Multivariate logistic regression (using age, sex and BMI as clinically significant variables and diabetes duration, Crt, albuminuria and genotype as statistically significant variables) was then used to determine independent associations and adjusted odds ratios (OR). The DD genotype was the strongest independent predictor of hypertension [P=0.029, OR=3.122, 95% confidence interval (CI)=1.127-8.647], followed by log (albuminuria) (P=0.042, OR=1.183, 95% CI=1.006-1.391). Considering albuminuria as a categorical variable did not change the results significantly.
The DD polymorphism in the ACE gene is independently associated with hypertension in the diabetic population.
关于血管紧张素转换酶(ACE)基因多态性与高血压之间关联的观察结果并不一致,这可能归因于种族和地域差异。此外,糖尿病患者群体中插入/缺失(I/D)多态性与高血压之间的关系尚未得到充分研究。本研究的目的是首次评估伊朗糖尿病成年人群中I/D多态性与高血压之间可能存在的关联。
总共纳入了82例连续的2型糖尿病合并高血压患者(A组)和87例2型糖尿病但无高血压患者(B组)。排除糖尿病发病前有高血压病史以及有提示继发性高血压体征的患者。为每位患者测定以下变量:年龄、性别、体重指数(BMI)、糖尿病病程及所用药物、冠状动脉疾病及其并发症史、血压(收缩压和舒张压)、空腹血糖(FBS)、糖化血红蛋白(HbA1c)、总胆固醇(Chol)、低密度脂蛋白(LDL)、高密度脂蛋白(HDL)、甘油三酯(TG)、血肌酐(Crt)和24小时尿白蛋白排泄量。采用聚合酶链反应(PCR)检测I/D等位基因。应用单因素分析(卡方检验和t检验)和多因素分析(校正比值比的多因素二元逻辑回归)来确定I/D多态性(以基因型II为参照)与高血压之间的关联。P<0.05被认为具有统计学意义。
在单因素分析中,除糖尿病病程(A组为156.05±73.54个月,B组为121.74±65.53个月;P=0.002)、Crt(A组为1.04±0.25mg/dl,B组为0.93±0.23mg/dl;P=0.003)、蛋白尿(A组为486.25±484.60mg/d,B组为316.50±459.56mg/d;P=0.021)以及DD基因型频率(A组27例,B组11例;P=0.026)外,两组在所有变量上均无统计学差异。然后采用多因素逻辑回归(将年龄、性别和BMI作为具有临床意义的变量,将糖尿病病程、Crt、蛋白尿和基因型作为具有统计学意义的变量)来确定独立关联和校正比值比(OR)。DD基因型是高血压最强的独立预测因素[P=0.029,OR=3.来22,95%置信区间(CI)=1.127 - 8.647],其次是log(蛋白尿)(P=0.042,OR=1.183,95%CI=1.006 - 1.391)。将蛋白尿视为分类变量并未显著改变结果。
ACE基因中的DD多态性与糖尿病患者群体中的高血压独立相关。