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布那唑嗪和阿替洛尔对肥胖的原发性高血压非糖尿病患者糖代谢的影响。

Effect of bunazosin and atenolol on glucose metabolism in obese, nondiabetic patients with primary hypertension.

作者信息

Bönner G, Schmieder R, Chrosch R, Weidinger G

机构信息

Department of Internal Medicine II, University of Cologne, Köln, Germany.

出版信息

Cardiovasc Drugs Ther. 1997 Mar;11(1):21-6. doi: 10.1023/a:1007735420758.

Abstract

Antihypertensive drugs, recommended by the World Health Organization for use in monotherapy, exert different effects on glucose and lipid metabolism. In our study we compared the effects of the beta-blocker atenolol (AT) and the alpha1-blocker bunazosin (BU) on glucose metabolism. The doses administered were chosen to produce similar antihypertensive effects with both drugs. The study was conducted as a bicenter, parallel, controlled, and double-blind study. All patients suffered from mild to moderate primary hypertension, were obese (body mass index > 26 kg/m2), but were nondiabetic. After a drug-free period of 4 weeks, patients were treated either with 6 and 12 mg of bunazosin (n = 15) or with 50 and 100 mg of atenolol (n = 17) once daily for 12 weeks. Glucose metabolism was measured by the iv glucose tolerance test (GTT) and the euglycemic hyperinsulinemic clamp test. The results show a similar blood pressure reduction with both drugs. However, their effects on glucose metabolism were significantly (p < 0.05) different: The area under the curve (AUC) of glucose in the iv GTT increased 26.8% during atenolol treatment but decreased 30% during bunazosin treatment. The same influence on the AUC of insulin was observed [AT +478.5 +/- 441.8 (+22%) vs. BU, -588.5 +/- 411.1 (-22%)]. Similar changes were found in the glucose clamp test. The metabolic clearance rate increased 11.4% during bunazosin use and decreased 8.4% during atenolol use to the same degree that the insulin sensitivity index changed (BU +13.2% vs. AT -21.9%). The differences between the two treatment regimes were statistically significant (p < 0.05). These results in obese hypertensives confirm the well-known negative effects of beta-blockers on glucose metabolism. Additionally, they demonstrate that an alpha1-blocker such as bunazosin develops the same blood pressure-lowering effect as beta-blockers, but with a significantly better profile with regard to glucose metabolism. Therefore, the use of alpha1-blockers can be recommended for obese hypertensives without any special care for glucose metabolism.

摘要

世界卫生组织推荐用于单一疗法的抗高血压药物,对葡萄糖和脂质代谢有不同影响。在我们的研究中,我们比较了β受体阻滞剂阿替洛尔(AT)和α1受体阻滞剂布那唑嗪(BU)对葡萄糖代谢的影响。所给药的剂量选择为使两种药物产生相似的抗高血压作用。该研究作为一项双中心、平行、对照和双盲研究进行。所有患者患有轻度至中度原发性高血压,均为肥胖者(体重指数>26kg/m2),但均非糖尿病患者。经过4周的无药期后,患者分别接受6mg和12mg布那唑嗪(n = 15)或50mg和100mg阿替洛尔(n = 17)治疗,每日一次,持续12周。通过静脉葡萄糖耐量试验(GTT)和正常血糖高胰岛素钳夹试验测量葡萄糖代谢。结果显示两种药物的血压降低程度相似。然而,它们对葡萄糖代谢的影响有显著差异(p < 0.05):静脉GTT中葡萄糖的曲线下面积(AUC)在阿替洛尔治疗期间增加了26.8%,而在布那唑嗪治疗期间降低了30%。观察到对胰岛素AUC有相同影响[阿替洛尔+478.5±441.8(+22%)与布那唑嗪,-588.5±411.1(-22%)]。在葡萄糖钳夹试验中发现了类似变化。布那唑嗪使用期间代谢清除率增加11.4%,阿替洛尔使用期间降低8.4%,与胰岛素敏感性指数变化程度相同(布那唑嗪+13.2%与阿替洛尔-21.9%)。两种治疗方案之间的差异具有统计学意义(p < 0.05)。这些肥胖高血压患者的结果证实了β受体阻滞剂对葡萄糖代谢的众所周知的负面影响。此外,它们表明像布那唑嗪这样的α1受体阻滞剂产生与β受体阻滞剂相同的降压效果,但在葡萄糖代谢方面有明显更好的表现。因此,对于肥胖高血压患者,无需对葡萄糖代谢进行任何特殊护理即可推荐使用α1受体阻滞剂。

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