Feher M D, Henderson A D, Wadsworth J, Poulter C, Gelding S, Richmond W, Sever P S, Elkeles R S
Department of Clinical Pharmacology, St. Mary's Hospital Medical School, London, UK.
J Hum Hypertens. 1990 Oct;4(5):571-7.
Hyperglycaemia, a raised fibrinogen, an increased serum triglyceride and a reduced HDL-cholesterol are common metabolic features of non-insulin dependent diabetes mellitus (NIDDM). Hypertension is frequently associated with NIDDM, however the influence of antihypertensive therapy on these combined factors in the diabetic is at present unclear. In a double-blind placebo-controlled crossover study in 20 stable NIDDM subjects with hypertension, the metabolic effects of 6 weeks' treatment with the alpha-blocker, doxazosin, was compared with treatment with the beta-blocker, atenolol. Similar and significant reductions in BP were produced by both drugs. Significant increases in weight, HbA1, apoprotein B, serum triglyceride and cholesterol/HDL ratio were observed with atenolol therapy. Doxazosin therapy was associated with opposite patterns of changes in fasting glucose, lipids and lipoproteins but only for serum triglyceride was difference between treatments significant. Fibrinogen was not altered by either treatment. Conclusions from this study indicate; 1) adrenergic mechanisms may be an important influence on glucose homeostasis and lipid metabolism in NIDDM and 2) the beta-blocker, atenolol, has a small adverse effect on weight, glycaemic control and the atherogenic lipid profile, whereas the alpha-blocker, doxazosin, has no such effect and may, in part, correct the disturbances of lipoprotein metabolism characteristic of NIDDM.
高血糖、纤维蛋白原升高、血清甘油三酯增加以及高密度脂蛋白胆固醇降低是非胰岛素依赖型糖尿病(NIDDM)常见的代谢特征。高血压常与NIDDM相关,但目前尚不清楚抗高血压治疗对糖尿病患者这些综合因素的影响。在一项针对20名患有高血压的稳定NIDDM患者的双盲安慰剂对照交叉研究中,比较了α受体阻滞剂多沙唑嗪6周治疗与β受体阻滞剂阿替洛尔治疗的代谢效应。两种药物均使血压产生了相似且显著的降低。阿替洛尔治疗后观察到体重、糖化血红蛋白、载脂蛋白B、血清甘油三酯和胆固醇/高密度脂蛋白比值显著增加。多沙唑嗪治疗与空腹血糖、脂质和脂蛋白的相反变化模式相关,但仅血清甘油三酯的治疗差异具有显著性。两种治疗均未改变纤维蛋白原。该研究的结论表明:1)肾上腺素能机制可能对NIDDM患者的葡萄糖稳态和脂质代谢有重要影响;2)β受体阻滞剂阿替洛尔对体重、血糖控制和致动脉粥样硬化的脂质谱有轻微不良影响,而α受体阻滞剂多沙唑嗪没有此类影响,且可能部分纠正NIDDM特有的脂蛋白代谢紊乱。