Wu Z, Bao X
Zhong Shan Hospital, Shanghai Medical University, PR China.
Clin Nephrol. 1998 Aug;50(2):108-12.
This study tested whether the angiotensin-converting enzyme inhibitor (ACEI) benazepril can improve the insulin resistance and glucose tolerance in uremia. Fifteen uremic hypertensive patients were treated with benazepril in a dose of 10-20 mg per day for ten weeks, and ten healthy subjects, matched in age, sex ratio and body mass index (BMI), served as the control group. Before and after the treatment, an oral 75 g glucose tolerance test (OGTT) and insulin release test (IRT) were performed in two groups above, and the blood glucose and serum insulin concentrations at 0, 60, 120 and 180 minutes after glucose load were examined, and the insulin glycoregulatory activity, including insulin sensitivity index (ISI), glucose uptake rate (M), total areas under the glucose and insulin curves during OGTTs (AUCG AUCINS), was calculated. The changes of serum potassium and renal function before and after treatment were observed. It showed that (1) benazepril could reduce blood pressure significantly (SBP decreased from 174.8 +/- 12.0 mmHg to 151.5 +/- 9.0 mmHg, p <0.001; DBP decreased from 108.0 +/- 8.2 mmHg to 95.3 +/- 9.0 mmHg, p <0.001). The total response rate was 86.7%. (2) After treatment with benazepril for ten weeks, the blood glucose and serum insulin concentrations after glucose load and AUCG, AUCINS values in the uremic patients were significantly lower than before treatment, but were still significantly higher than in the controls. The values of ISI and M in the uremic patients after treatment were much higher than before treatment, but were still significantly lower than in the control subjects. (3) The differences of serum potassium and creatinine levels before and after treatment were not significant. These findings indicate that benazepril can not only reduce blood pressure effectively and safely, but also partly improve insulin resistance, hyperinsulinemia and glucose intolerance in uremia.
本研究检测血管紧张素转换酶抑制剂(ACEI)苯那普利是否能改善尿毒症患者的胰岛素抵抗和糖耐量。15例尿毒症高血压患者接受苯那普利治疗,剂量为每日10 - 20 mg,共治疗10周,10例年龄、性别比和体重指数(BMI)相匹配的健康受试者作为对照组。治疗前后,对上述两组进行口服75 g葡萄糖耐量试验(OGTT)和胰岛素释放试验(IRT),检测葡萄糖负荷后0、60、120和180分钟时的血糖和血清胰岛素浓度,并计算胰岛素糖调节活性,包括胰岛素敏感指数(ISI)、葡萄糖摄取率(M)、OGTT期间葡萄糖和胰岛素曲线下总面积(AUCG、AUCINS)。观察治疗前后血清钾和肾功能的变化。结果显示:(1)苯那普利能显著降低血压(收缩压从174.8±12.0 mmHg降至151.5±9.0 mmHg,p<0.001;舒张压从108.0±8.2 mmHg降至95.3±9.0 mmHg,p<0.001)。总有效率为86.7%。(2)苯那普利治疗10周后,尿毒症患者葡萄糖负荷后的血糖和血清胰岛素浓度以及AUCG、AUCINS值均显著低于治疗前,但仍显著高于对照组。治疗后尿毒症患者的ISI和M值远高于治疗前,但仍显著低于对照组。(3)治疗前后血清钾和肌酐水平差异无统计学意义。这些研究结果表明,苯那普利不仅能有效、安全地降低血压,还能部分改善尿毒症患者的胰岛素抵抗、高胰岛素血症和糖耐量异常。