卡托普利长期治疗对高血压糖尿病患者微量和大量蛋白尿的影响。

P Vörös, Z Lengyel, C Németh, S Mirzahosseini, L Kammerer, L Rosivall
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引用次数: 2

摘要

在卡托普利治疗开始后,对高血压胰岛素依赖型糖尿病患者进行了为期4年的微量蛋白尿[16]和大量蛋白尿[17]的随访,以评估ACE抑制剂治疗对蛋白尿和血压正常化的疗效。在卡托普利治疗的前6个月内,微蛋白尿和大蛋白尿患者的平均收缩压分别从168.1 +/- 17.6 mmHg降至134.4 +/- 12.1 mmHg(19.2 +/- 7.1%)和从177.6 +/- 16.8 mmHg降至143.5 +/- 12.7 (18.9 +/- 6.7%)mmHg。同样,微白蛋白尿组的平均舒张压从91.9 +/- 9.1 mmHg降至74.4 +/- 10.3 mmHg(19.0 +/- 9.4%),大白蛋白尿组从95.3 +/- 13.7 mmHg降至78.2 +/- 7.3 (16.9 +/- 9.5%)mmHg。卡托普利给药6个月后,微量和大量蛋白尿组的白蛋白排泄率也分别从97.4 +/- 35.9微克/分钟下降到51.9 +/- 19.9微克/分钟(46.9 +/- 7.6%)和从766.7 +/- 577.9微克/分钟下降到365.1 +/- 298.4微克/分钟(50.4 +/- 8.4%)。此后,平均白蛋白排泄率和血压显著升高,但在第四年结束时,与预处理期相比,它们仍显著降低。4年后,微量蛋白尿组的白蛋白排泄率为71.3 +/- 29.6微克/分钟,而大量蛋白尿组的白蛋白排泄率为391.2 +/- 204.7微克/分钟。我们得出结论,ACE抑制剂治疗导致蛋白尿和血压迅速下降,尽管缓慢逐渐增加,但四年后白蛋白排泄率和血压值仍显着低于初始值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The efficacy of long-term captopril treatment on micro- and macroalbuminuria in hypertensive diabetics.

Microalbuminuric [16] and macroalbuminuric [17] hypertensive insulin dependent diabetics were followed up for 4 years after the initiation of captopril therapy to assess the efficacy of ACE inhibitor therapy on albuminuria and blood pressure normalisation. Within the first six months of captopril therapy mean systolic blood pressure decreased in microalbuminuric and macroalbuminuric patients from 168.1 +/- 17.6 mmHg to 134.4 +/- 12.1 mmHg (19.2 +/- 7.1%) and from 177.6 +/- 16.8 mmHg to 143.5 +/- 12.7 (18.9 +/- 6.7%) mmHg, respectively. Mean diastolic blood pressure, similarly, showed a decrease from 91.9 +/- 9.1 mmHg to 74.4 +/- 10.3 mmHg (19.0 +/- 9.4%) in the microalbuminuric and from 95.3 +/- 13.7 mmHg to 78.2 +/- 7.3 (16.9 +/- 9.5%) mmHg in the macroalbuminuric group. After six months of captopril administration albumin excretion rates decreased as well, from 97.4 +/- 35.9 micrograms/min to 51.9 +/- 19.9 micrograms/min (46.9 +/- 7.6%) and from 766.7 +/- 577.9 micrograms/min to 365.1 +/- 298.4 micrograms/min (50.4 +/- 8.4%) in the micro- and macroalbuminuric groups, respectively. Thereafter, mean albumin excretion rates and blood pressure rose significantly, but at the end of the fourth year they were still significantly lower compared to that of the pretreatment period. After four years, albumin excretion rates were 71.3 +/- 29.6 micrograms/min in the microalbuminuric and 391.2 +/- 204.7 micrograms/min in the macroalbuminuric group. We conclude that ACE inhibitor therapy results in a rapid decrease of albuminuria and blood pressure, and despite a slow gradual increase, the albumin excretion rates and blood pressure values remain significantly lower than the initial values after four years.

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