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在中国人群慢性肾脏病患者中血管紧张素转换酶和血管紧张素 II 型 1 受体的基因多态性。

Gene polymorphisms of angiotensin-converting enzyme and angiotensin II type 1 receptor among chronic kidney disease patients in a Chinese population.

机构信息

School of Public Health, National Defense Medical Center, Taipei, Taiwan, ROC.

出版信息

J Renin Angiotensin Aldosterone Syst. 2012 Mar;13(1):148-54. doi: 10.1177/1470320311430989. Epub 2011 Dec 6.

DOI:10.1177/1470320311430989
PMID:22147663
Abstract

Chronic kidney disease (CKD) is highly prevalent in Taiwan and an increasing number of patients are affected, with a high risk of progression to end-stage renal disease and huge medical expenses. It has been predicted that the presence of hypertension increases with decreasing renal function due to a decrease in sodium excretion and activation of the renin-angiotensin system (RAS). The aim of this study was to investigate the influence of genetic variants of the RAS gene on CKD. We performed a case control association study and genotyped 135 CKD patients and 270 healthy controls among Han Chinese in Taiwan. All subjects were genotyped for angiotensinogen (AGT-M235T, T174M, A-20C), angiotensin-I converting enzyme (ACE-A2350G) and angiotensin II type 1 receptor (AGTR1-A1166C, C573T, C-521T) polymorphisms of RAS genes by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis. Significant associations were observed in ACE-A2350G and AGTR1-C573T polymorphism between CKD patients and controls. In regard to ACE-A2350G, compared with the AA genotype the GG genotype protected against CKD (adjusted odds ratio [OR] = 0.34; p = 0.01). In regard to AGTR1-C573T, the CT genotype was a risk for CKD compared with the CC genotype (adjusted OR = 1.82; p = 0.03). We conclude that ACE-A2350G and AGTR1-C573T polymorphisms are likely candidate determinants of CKD.

摘要

慢性肾脏病(CKD)在台湾地区非常普遍,越来越多的患者受到影响,进展为终末期肾病的风险较高,医疗费用巨大。由于钠排泄减少和肾素-血管紧张素系统(RAS)的激活,预计随着肾功能的降低,高血压的发生率会增加。本研究旨在探讨 RAS 基因的遗传变异对 CKD 的影响。我们进行了病例对照关联研究,对台湾汉族的 135 名 CKD 患者和 270 名健康对照进行了基因分型。所有受试者均通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析对 RAS 基因的血管紧张素原(AGT-M235T、T174M、A-20C)、血管紧张素转换酶(ACE-A2350G)和血管紧张素 II 型 1 受体(AGTR1-A1166C、C573T、C-521T)多态性进行了基因分型。在 CKD 患者和对照组之间,ACE-A2350G 和 AGTR1-C573T 多态性存在显著相关性。在 ACE-A2350G 方面,与 AA 基因型相比,GG 基因型可降低 CKD 的发病风险(调整后的优势比[OR] = 0.34;p = 0.01)。在 AGTR1-C573T 方面,与 CC 基因型相比,CT 基因型是 CKD 的危险因素(调整后的 OR = 1.82;p = 0.03)。我们得出结论,ACE-A2350G 和 AGTR1-C573T 多态性可能是 CKD 的候选决定因素。

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