McLaughlin D M, Atkinson A B, Ennis C N, Browne J, Hunter S J, Sheridan B, Bell P M
Regional Centre for Endocrinology and Diabetes, Royal Victoria Hospital, Belfast, UK.
Diabet Med. 2008 May;25(5):631-4. doi: 10.1111/j.1464-5491.2008.02437.x.
To establish the safety in terms of insulin sensitivity of a low dose thiazide/ACE inhibitor combination.
We examined the effects on insulin sensitivity of captopril either alone or in combination with low-dose bendroflumethiazide (1.25 mg) in 15 hypertensive Type 2 diabetic patients. Insulin action was assessed using an isoglycaemic hyperinsulinaemic clamp in a double-blind, randomised, crossover study after a 6-week placebo run-in and following two 12-week treatment periods with captopril (C) (100 mg) alone or in combination with bendroflumethiazide (CB) (1.25 mg).
Blood pressure was lower following CB compare to C (138/83 vs. 144/85 mmHg; P < 0.05) and both were lower than baseline (153/92 mmHg; P < 0.01). CB resulted in a significant increase in fasting plasma glucose compared to C (9.6 +/- 2.6 vs. 8.5 +/- 1.6 mmol/l; P < 0.05). Exogenous glucose infusion rates required to maintain isoglycaemia during hyperinsulinaemia were lower after CB compared to C (25.1 +/- 13.3 vs. 34.2 +/- 16.8 micromol/kg/min; P < 0.01) as were isotopically determined glucose utilisation rates (29.0 +/- 12.4 vs. 36.6 +/- 17.3 micromol/kg/min; P < 0.05). There was no significant difference in fasting endogenous glucose production between treatments (CB 9.3 +/- 3.3 vs. C 8.6 +/- 1.6 micromol/kg/min), nor between suppression following insulin (CB 4.0 +/- 2.1 vs. C 4.3 +/- 3.1 micromol/kg/min).
Combination of low-dose bendroflumethiazide with captopril lowered blood pressure but resulted in deleterious effects on insulin action compared to captopril alone.
确定低剂量噻嗪类药物/血管紧张素转换酶抑制剂联合用药在胰岛素敏感性方面的安全性。
我们在15例高血压2型糖尿病患者中,研究了卡托普利单独使用或与低剂量苄氟噻嗪(1.25毫克)联合使用对胰岛素敏感性的影响。在为期6周的安慰剂导入期后,以及在两个为期12周的治疗期,分别单独使用卡托普利(C)(100毫克)或与苄氟噻嗪(CB)(1.25毫克)联合使用后,通过双盲、随机、交叉研究,使用等血糖高胰岛素钳夹技术评估胰岛素作用。
与单独使用卡托普利相比,联合使用苄氟噻嗪后血压更低(138/83对144/85毫米汞柱;P<0.05),且两者均低于基线水平(153/92毫米汞柱;P<0.01)。与单独使用卡托普利相比,联合使用苄氟噻嗪导致空腹血糖显著升高(9.6±2.6对8.5±1.6毫摩尔/升;P<0.05)。与单独使用卡托普利相比,联合使用苄氟噻嗪后在高胰岛素血症期间维持等血糖所需的外源性葡萄糖输注率更低(25.1±13.3对34.2±16.8微摩尔/千克/分钟;P<0.01),同位素测定的葡萄糖利用率也是如此(29.0±12.4对36.6±17.3微摩尔/千克/分钟;P<0.05)。治疗之间空腹内源性葡萄糖生成无显著差异(联合使用苄氟噻嗪为9.3±3.3对单独使用卡托普利为8.6±1.6微摩尔/千克/分钟),胰岛素抑制后也无显著差异(联合使用苄氟噻嗪为4.0±2.1对单独使用卡托普利为4.3±3.1微摩尔/千克/分钟)。
与单独使用卡托普利相比,低剂量苄氟噻嗪与卡托普利联合用药可降低血压,但对胰岛素作用产生有害影响。