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氨氯地平和赖诺普利对原发性高血压患者微量白蛋白尿的影响:一项前瞻性研究。

Effect of amlodipine and lisinopril on microalbuminuria in patients with essential hypertension: A prospective study.

作者信息

Jalal S, Sofi F A, Abass S M, Alai M S, Bhat M A, Rather H A, Lone N A, Siddiqi M A

机构信息

Department of Cardiology, Sher-i-Kashmir Institute of Medical Sciences, (SKIMS), Soura, Srinagar, Kashmir, India.

出版信息

Indian J Nephrol. 2010 Jan;20(1):15-20. doi: 10.4103/0971-4065.62090.

Abstract

Microalbuminuria can be present in 25-100% of patients with essential hypertension and is associated with increased incidence of cardiovascular events. Our goal was to evaluate the effect of a commonly used calcium channel blocker, amlodipine, and an angiotensin converting enzyme inhibitor, lisinopril on urinary albumin excretion in patients with mild to moderate essential hypertension. We screened 324 patients with essential hypertension for microalbuminuria and documented it in 120 patients. These 120 patients with microalbuminuria were randomly divided into two groups of 60 each, matched for age, sex, arterial pressure, creatinine clearance, and urinary albumin excretion so as to receive amlodipine or lisinopril. We prospectively measured their urinary albumin excretion and creatinine clearance prior to treatment and, four and eight weeks after treatment with amlodipine or lisinopril. Mean arterial pressure (mean +/- SD) at baseline, after four weeks, and after eight weeks was 113.01 +/- 4.38,104.93 +/- 3.12, and 98.89 +/- 1.75 mmHg (P < 0.0000); and 114.13 +/- 7.11, 106.52 +/- 3.50, and 100.89 +/- 2.80 mmHg (P < 0.0000) in amlodipine and lisinopril groups, respectively. Urinary albumin excretion (mean +/- SEM) at baseline, after four, and after eight weeks was 79.30 +/- 3.74, 62.03 +/- 3.61, and 52.02 +/- 3.05 (P < 0.0000); and 73.96 +/- 4.10, 72.39 +/- 3.74, 66.12 +/- 3.94 (P = 0.1742) in lisinopril and amlodipine groups, respectively. Lisinopril but not amlodipine, reduced the urinary albumin excretion significantly despite their similar antihypertensive efficacy. The clinical and prognostic significance of these observations need to be established.

摘要

微量白蛋白尿可见于25%至100%的原发性高血压患者中,且与心血管事件发生率增加相关。我们的目标是评估常用钙通道阻滞剂氨氯地平和血管紧张素转换酶抑制剂赖诺普利对轻度至中度原发性高血压患者尿白蛋白排泄的影响。我们对324例原发性高血压患者进行了微量白蛋白尿筛查,其中120例被确诊。这120例微量白蛋白尿患者被随机分为两组,每组60例,两组在年龄、性别、动脉压、肌酐清除率和尿白蛋白排泄方面相匹配,分别接受氨氯地平或赖诺普利治疗。我们前瞻性地测量了他们在治疗前以及接受氨氯地平或赖诺普利治疗4周和8周后的尿白蛋白排泄和肌酐清除率。氨氯地平和赖诺普利组在基线、4周后和8周后的平均动脉压(均值±标准差)分别为113.01±4.38、104.93±3.12和98.89±1.75 mmHg(P<0.0000);以及114.13±7.11、106.52±3.50和100.89±2.80 mmHg(P<0.0000)。氨氯地平和赖诺普利组在基线、4周后和8周后的尿白蛋白排泄(均值±标准误)分别为79.30±3.74、62.03±3.61和52.02±3.05(P<0.0000);以及73.96±4.10、72.39±3.74和66.12±3.94(P=0.1742)。尽管氨氯地平和赖诺普利的降压效果相似,但只有赖诺普利能显著降低尿白蛋白排泄。这些观察结果的临床和预后意义有待确定。

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