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原发性高血压中的微量白蛋白尿。不同降压药物的降低作用。

Microalbuminuria in essential hypertension. Reduction by different antihypertensive drugs.

作者信息

Erley C M, Haefele U, Heyne N, Braun N, Risler T

机构信息

University of Tübingen, Department of Nephrology and Hypertension, FRG.

出版信息

Hypertension. 1993 Jun;21(6 Pt 1):810-5. doi: 10.1161/01.hyp.21.6.810.

Abstract

The effects of four different antihypertensive drugs (the Ca(2+)-channel blocker felodipine, the beta-blocker metoprolol, the angiotensin converting enzyme inhibitor ramipril, and the alpha-blocking agent doxazosin) on microalbuminuria and renal hemodynamics were evaluated in a double-blind, crossover study in 17 patients (10 women, seven men, aged 39 +/- 14 years) with mild-to-moderate essential arterial hypertension and microalbuminuria. Patients were studied after a 2-week placebo phase preceded by 2 weeks off all medication and after 12 weeks of treatment with each drug. Between each drug treatment, there was another 14-day placebo washout period. At the end of the study, we performed two additional 2-week placebo periods. After each placebo and treatment period, we measured albumin excretion during a 3-day collecting period. Renal hemodynamics were assessed by clearance techniques (inulin and p-aminohippurate clearance) at the end of the first and last placebo periods and after each treatment period. All drugs reduced mean arterial pressure and microalbuminuria to a similar and statistically significant (p < 0.05) extent (mean arterial pressure: placebo phase, 116 +/- 5 mm Hg; felodipine, 101 +/- 4 mm Hg; metoprolol, 101 +/- 5 mm Hg; ramipril, 101 +/- 4 mm Hg; doxazosin, 102 +/- 5 mm Hg; urinary albumin excretion: placebo phase, 46 +/- 50 mg/day; felodipine, 18 +/- 23 mg/day; metoprolol, 14 +/- 12 mg/day; ramipril, 16 +/- 16 mg/day; doxazosin, 14 +/- 14 mg/day). Mean arterial pressure levels and urinary albumin excretion returned to baseline after the last placebo period (110 +/- 6 mm Hg and 40 +/- 46 mg/day, respectively).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在一项双盲、交叉研究中,对17例(10名女性,7名男性,年龄39±14岁)患有轻至中度原发性高血压和微量白蛋白尿的患者,评估了四种不同降压药物(钙通道阻滞剂非洛地平、β受体阻滞剂美托洛尔、血管紧张素转换酶抑制剂雷米普利和α受体阻滞剂多沙唑嗪)对微量白蛋白尿和肾脏血流动力学的影响。患者在停用所有药物2周后经过2周的安慰剂阶段,然后接受每种药物治疗12周。在每种药物治疗之间,还有一个14天的安慰剂洗脱期。在研究结束时,又进行了两个为期2周的安慰剂阶段。在每个安慰剂期和治疗期结束后,我们在3天的收集期内测量白蛋白排泄量。在第一个和最后一个安慰剂期结束时以及每个治疗期后,通过清除技术(菊粉和对氨基马尿酸清除率)评估肾脏血流动力学。所有药物均将平均动脉压和微量白蛋白尿降低到相似且具有统计学意义(p<0.05)的程度(平均动脉压:安慰剂阶段,116±5mmHg;非洛地平,101±4mmHg;美托洛尔,101±5mmHg;雷米普利,101±4mmHg;多沙唑嗪,102±5mmHg;尿白蛋白排泄量:安慰剂阶段,46±50mg/天;非洛地平,18±23mg/天;美托洛尔,14±12mg/天;雷米普利,16±16mg/天;多沙唑嗪,14±14mg/天)。在最后一个安慰剂期后,平均动脉压水平和尿白蛋白排泄量恢复到基线(分别为110±6mmHg和40±46mg/天)。(摘要截断于250字)

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