Lee Y-T, Chiu H-C, Huang C-T, Su H-M, Wang C-L, Lin T-H, Voon W-C, Chen H-C, Lai W-T, Sheu S-H
Division of Nephrology, Department of Pediatric, Kaohsiung Medical University Hospital, Kaohsiung 80708, Taiwan.
Clin Nephrol. 2009 Dec;72(6):457-67. doi: 10.5414/cnp72457.
The angiotensin II Type 1 receptor (AT1R) A1166C (rs5186) genez polymorphism is equivocally associated with the patients' susceptibility to chronic kidney disease or end-stage renal disease. We conducted a prospective study to investigate the influence of AT1R A1166C gene polymorphism on the quantitative changes of renal function.
Of 1500 people screened, 112 non-diabetic normotensive elderly Chinese were recruited and received biochemistry examination at the baseline, at the second and fourth year follow-up. Serum creatinine and calculated renal parameters, using Cockroft-Gault (CG) formula, Modification of Diet in Renal Disease (MDRD) Study and abbreviated MDRD (abMDRD) equation, were used to evaluate renal function and their progression. Genotyping was performed by polymerase chain reaction-restriction fragment length polymorphism.
Age was 71.9 +/- 3.7 years (range 60 - 81). Serum creatinine, CG creatinine clearance (CrCl), MDRD and abMDRD glomerular filtration rate (GFR) were significantly decreased at the 2 and 4-year follow-up (all p < 0.001). The magnitude of 4-year decline of above four renal parameters was significantly higher in subjects carrying the AT1R AA genotype than C-allele carriers (p = 0.014, 0.033, 0.008 and 0.014 for creatinine, CG CrCl, MDRD and abMDRD GFR, respectively). This association was still significant in multivariate analyses (p = 0.019, 0.045, 0.035 and 0.018, respectively).
This longitudinal study showed that the aging process was associated with decline of renal function in the healthy elderly. The AT1R A1166C gene polymorphism might modulate these changes in the Chinese. This provides further knowledge essential in the assessment of renal disease and determination of renal function in the older subjects.
血管紧张素II 1型受体(AT1R)A1166C(rs5186)基因多态性与患者对慢性肾脏病或终末期肾病的易感性之间的关联尚不明确。我们进行了一项前瞻性研究,以调查AT1R A1166C基因多态性对肾功能定量变化的影响。
在1500名接受筛查的人群中,招募了112名非糖尿病血压正常的中国老年患者,在基线、随访的第二年和第四年接受生化检查。使用Cockroft-Gault(CG)公式、肾脏病饮食改良(MDRD)研究公式和简化的MDRD(abMDRD)公式计算血清肌酐和肾脏参数,以评估肾功能及其进展情况。通过聚合酶链反应-限制性片段长度多态性进行基因分型。
年龄为71.9±3.7岁(范围60 - 81岁)。在随访的第2年和第4年,血清肌酐、CG肌酐清除率(CrCl)、MDRD和abMDRD肾小球滤过率(GFR)均显著下降(所有p<0.001)。携带AT1R AA基因型的受试者上述四项肾脏参数4年下降幅度显著高于携带C等位基因的受试者(肌酐、CG CrCl、MDRD和abMDRD GFR分别为p = 0.014、0.033、0.008和0.014)。在多变量分析中,这种关联仍然显著(分别为p = 0.019、0.045、0.035和0.018)。
这项纵向研究表明,衰老过程与健康老年人的肾功能下降有关。AT1R A1166C基因多态性可能会调节中国人的这些变化。这为评估老年受试者的肾脏疾病和确定肾功能提供了进一步的重要知识。