Ko Gang Jee, Kang Young Sun, Lee Mi Hwa, Song Hye Kyoung, Kim Hyoung Kyu, Cha Dae Ryong
Department of Internal Medicine, Korea University, Ansan City, Kyungki-Do, Seoul, Korea.
Nephrology (Carlton). 2008 Dec;13(6):492-9. doi: 10.1111/j.1440-1797.2008.01005.x. Epub 2008 Sep 1.
Inhibition of aldosterone system is beneficial in diabetic nephropathy, and aldosterone synthesis is regulated at the gene-encoding aldosterone synthase (CYP11B2). Considering the role of aldosterone in diabetic nephropathy, genetic polymorphism of this gene may contribute to the development and progression of diabetic nephropathy. In this study, we investigated whether it is associated with diabetic nephropathy in type 2 diabetic patients.
197 type 2 diabetic patients and 71 healthy controls were enrolled. The study subjects were divided into four groups: healthy controls with normoalbuminuria (n = 71), normoalbuminuric diabetic group (n = 71), microalbuminuric diabetic group (n = 51) and overt proteinuria group (n = 51). Polymorphism of aldosterone synthase gene was determined using standard PCR technique.
Higher frequency of TT genotype and T allele in steroidogenic factor-1 (SF-1) binding site and wild type (WT) in intronic conversion (IC) in CYP11B2 was observed in diabetic patients than controls. However, there was no significant difference in SF-1 and IC genotype among diabetic patients according to the state of diabetic nephropathy. Subgroup analysis based on SF-1 polymorphism demonstrated that TT genotype is associated with higher systolic and diastolic blood pressure and higher plasma aldosterone level. In addition, WT in IC genotype showed a significantly higher urinary albumin excretion rate. Plasma aldosterone level was significantly related with systolic blood pressure.
Our study suggests that aldosterone synthase gene polymorphism is not associated with progression of diabetic nephropathy, but it may contribute to the development of hypertension associated with increased aldosterone secretion in type 2 diabetic patients.
抑制醛固酮系统对糖尿病肾病有益,醛固酮的合成受醛固酮合酶(CYP11B2)编码基因的调控。鉴于醛固酮在糖尿病肾病中的作用,该基因的遗传多态性可能与糖尿病肾病的发生和发展有关。在本研究中,我们调查了其是否与2型糖尿病患者的糖尿病肾病相关。
纳入197例2型糖尿病患者和71例健康对照者。研究对象分为四组:正常白蛋白尿的健康对照组(n = 71)、正常白蛋白尿糖尿病组(n = 71)、微量白蛋白尿糖尿病组(n = 51)和显性蛋白尿组(n = 51)。采用标准PCR技术检测醛固酮合酶基因的多态性。
糖尿病患者中,CYP11B2基因类固醇生成因子-1(SF-1)结合位点的TT基因型和T等位基因以及内含子转换(IC)中的野生型(WT)频率高于对照组。然而,根据糖尿病肾病的状态,糖尿病患者中SF-1和IC基因型无显著差异。基于SF-1多态性的亚组分析表明,TT基因型与较高的收缩压和舒张压以及较高的血浆醛固酮水平相关。此外,IC基因型中的WT显示尿白蛋白排泄率显著更高。血浆醛固酮水平与收缩压显著相关。
我们的研究表明,醛固酮合酶基因多态性与糖尿病肾病的进展无关,但可能导致2型糖尿病患者中与醛固酮分泌增加相关的高血压的发生。