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螺普利与阿替洛尔的代谢效应:一项随机长期研究的结果

Metabolic effects of spirapril and atenolol: results from a randomized, long-term study.

作者信息

Hakamäki T, Lehtonen A

机构信息

Department of Medicine, Turku City Hospital, Turku, Finland.

出版信息

Int J Clin Pharmacol Ther. 1997 Jun;35(6):227-30.

PMID:9208336
Abstract

Thirty-seven patients with mild to moderate hypertension were randomized in a double-blind, parallell-group study to receive either 6 mg of spirapril or 50 mg of atenolol. After 6 weeks of treatment, the daily dose of spirapril was increased to 12 mg and the daily dose of atenolol to 100 mg, if the target diastolic pressure < or = 90 mmHg was not achieved. The total treatment period was 12 months for both drugs. There were no changes in the lipid levels in the spirapril treatment group whereas the concentration of apoprotein A1 decreased significantly (p < 0.05) in the group treated with atenolol when compared with baseline. There was a tendency in the levels of serum cholesterol and triglycerides to increase and in the level of HDL cholesterol to decrease in the atenolol treatment group compared with baseline. Fasting blood glucose levels did not change significantly in the treatment group when compared with baseline. The 2-hour blood glucose level in the glucose tolerance test increased significantly after the 12-month therapy with both spirapril (p < 0.05) and atenolol (p < 0.05) when compared with baseline levels. There was also a tendency in the 2-hour insulin levels to increase in both the spirapril and the atenolol treatment group after the 12-month treatment period. In conclusion, spirapril had no effect on lipid metabolism whereas atenolol had some untoward effects. In the group treated with atenolol fasting blood glucose levels increased, but both spirapril and atenolol increased the 2-hour blood glucose levels in the glucose tolerance test.

摘要

37例轻至中度高血压患者被随机纳入一项双盲平行组研究,分别接受6毫克螺普利或50毫克阿替洛尔治疗。治疗6周后,如果未达到目标舒张压≤90毫米汞柱,则将螺普利的每日剂量增至12毫克,阿替洛尔的每日剂量增至100毫克。两种药物的总治疗期均为12个月。螺普利治疗组的血脂水平无变化,而与基线相比,阿替洛尔治疗组的载脂蛋白A1浓度显著降低(p<0.05)。与基线相比,阿替洛尔治疗组的血清胆固醇和甘油三酯水平有升高趋势,高密度脂蛋白胆固醇水平有降低趋势。与基线相比,治疗组的空腹血糖水平无显著变化。与基线水平相比,用螺普利(p<0.05)和阿替洛尔(p<0.05)进行12个月治疗后,葡萄糖耐量试验中的2小时血糖水平均显著升高。在12个月的治疗期后,螺普利和阿替洛尔治疗组的2小时胰岛素水平也均有升高趋势。总之,螺普利对脂质代谢无影响,而阿替洛尔有一些不良影响。在阿替洛尔治疗组中,空腹血糖水平升高,但螺普利和阿替洛尔均使葡萄糖耐量试验中的2小时血糖水平升高。

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