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赖诺普利比硝苯地平能更有效地降低患有早期肾病的高血压II型糖尿病患者的尿白蛋白排泄量。

Greater reduction of urinary albumin excretion in hypertensive type II diabetic patients with incipient nephropathy by lisinopril than by nifedipine.

作者信息

Agardh C D, Garcia-Puig J, Charbonnel B, Angelkort B, Barnett A H

机构信息

Department of Internal Medicine, University Hospital, Lund, Sweden.

出版信息

J Hum Hypertens. 1996 Mar;10(3):185-92.

PMID:8733038
Abstract

A double-blind, randomised, parallel group, multicentre, multinational study compared the effects of 12 months' treatment with lisinopril (10-20 mg once daily) or nifedipine retard tablets (20-40 mg twice daily) in 239 males (aged 18-75 years) and 96 post-menopausal females (aged 40-75 years). They all had a history of clinically stable type II diabetes > 3 months, microalbuminuria and early diabetic nephropathy (a urinary albumin excretion (UAE) rate ranging from 20 to 300 micrograms/min) and a sitting diastolic blood pressure (DBP) 90-100 mm Hg (Korotkoff phase V) inclusive at both entry and after 3-4 weeks' placebo treatment. The aim of treatment was to achieve a reduction in sitting DBP to < 90 mm Hg 24-30 h after the last dose of lisinopril or 12-18 hours after the last dose of nifedipine and to evaluate the effect of these treatments on UAE over 12 months. The effect of the two treatments on ambulatory blood pressure (BP) was also evaluated in a subset of patients. Management of diabetes with oral hypoglycaemic drugs, diet and insulin alone or in combination was permitted. Median UAE fell on lisinopril from 65.5 (range 20-297) micrograms/min at baseline to 39.0 (2-510) micrograms/min after 12 months. On nifedipine median UAE fell from 63.0 (range 20-289) micrograms/min at baseline to 58.0 (9-1192) micrograms/min after 12 months. The estimated median difference between the effects of the two treatments was 20 micrograms/min (P = 0.0006). Over 12 months both treatments produced similar falls in sitting BP from 163 +/- 17/99 +/- 6 mm Hg (mean +/- s.d.) to 147 +/- 18/88 +/- 10 mm Hg for lisinopril and from 161 +/- 18/97 +/- 5 mm Hg to 150 +/- 18/88 +/- 9 mm Hg for nifedipine. Ambulatory BP was assessed in a subset of patients and using areas under the BP-time curve (AUC) a comparison of the effects of the two treatments showed no between-treatment differences. Creatinine clearance, glycaemic control (HbA1c) and lipid profiles did not change significantly during either treatment. Frequency of withdrawals and adverse events were similar for both treatments. We conclude that lisinopril has a significantly more beneficial effect on UAE than nifedipine despite similar effects on both BP and glycaemic control in type II diabetic patients with hypertension.

摘要

一项双盲、随机、平行组、多中心、跨国研究比较了赖诺普利(每日一次,10 - 20毫克)或缓释硝苯地平片(每日两次,20 - 40毫克)对239名男性(年龄18 - 75岁)和96名绝经后女性(年龄40 - 75岁)进行12个月治疗的效果。他们均有临床稳定的II型糖尿病病史超过3个月、微量白蛋白尿和早期糖尿病肾病(尿白蛋白排泄(UAE)率为20至300微克/分钟),且在入组时和3 - 4周安慰剂治疗后坐位舒张压(DBP)为90 - 100毫米汞柱(柯氏音第V期)。治疗目的是在最后一剂赖诺普利后24 - 30小时或最后一剂硝苯地平后12 - 18小时使坐位DBP降至<90毫米汞柱,并评估这些治疗在12个月内对UAE的影响。还在一部分患者中评估了两种治疗对动态血压(BP)的影响。允许单独或联合使用口服降糖药、饮食和胰岛素来管理糖尿病。赖诺普利治疗后,UAE中位数从基线时的65.5(范围20 - 297)微克/分钟降至12个月后的39.0(2 - 510)微克/分钟。硝苯地平治疗后,UAE中位数从基线时的63.0(范围20 - 289)微克/分钟降至12个月后的58.0(9 - 1192)微克/分钟。两种治疗效果的估计中位数差异为20微克/分钟(P = 0.0006)。在12个月内,两种治疗使坐位BP产生了相似的下降,赖诺普利组从163±17/99±6毫米汞柱(均值±标准差)降至147±18/88±10毫米汞柱,硝苯地平组从161±18/97±5毫米汞柱降至150±18/88±9毫米汞柱。在一部分患者中评估了动态血压,通过血压 - 时间曲线下面积(AUC)比较两种治疗效果,未发现治疗组间差异。在任何一种治疗期间,肌酐清除率、血糖控制(糖化血红蛋白)和血脂谱均无显著变化。两种治疗的停药频率和不良事件相似。我们得出结论,在患有高血压的II型糖尿病患者中,尽管赖诺普利和硝苯地平对BP和血糖控制的效果相似,但赖诺普利对UAE的有益作用明显大于硝苯地平。

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