Lithell H, Aberg H, Selinus I
Am J Med. 1986 Feb 14;80(2A):114-9. doi: 10.1016/0002-9343(86)90170-1.
Twenty hypertensive men, aged 58 to 62 years, who had been treated with a combination of different drugs for many years, had their therapy changed in a stepwise manner to a combination of 50 mg of atenolol per day and 2 to 15 mg of prazosin per day. The effects of each change of treatment were assessed separately five to six months after the change. Serum lipids and high-density lipoprotein concentrations were determined, and an intravenous glucose tolerance test was performed at the start of the study and after each change. In the group in which therapy was changed from a diuretic to prazosin, serum cholesterol and triglyceride concentrations decreased significantly by 11 and 42 percent, respectively, but in the group in which therapy was changed from hydralazine to prazosin, there were no alterations in serum lipids or lipoproteins. The changes in therapy had no overall effects on glucose or insulin parameters evaluated with an intravenous glucose tolerance test. However, prazosin was associated with an increase in the fasting blood glucose level and a decrease in the peak insulin value after glucose injection, both of which were dose-related effects. The data indicate that the glucose turnover was at least as good after a switch from diuretic to prazosin treatment as before at lower insulin values. In those patients in whom therapy was switched from propranolol to 50 mg of atenolol per day, the serum triglyceride concentration decreased by about 10 percent, whereas in the group in which therapy was changed from 100 to 50 mg of atenolol per day, there were no serum lipid or lipoprotein alterations. The results show that a combination of 50 mg of atenolol per day and prazosin has metabolic advantages over combined diuretic and propranolol treatment. Such advantages may be of importance in the long-term treatment of hypertensive patients.
20名年龄在58至62岁之间的高血压男性,多年来一直接受多种药物联合治疗,他们的治疗方案逐步改为每天服用50毫克阿替洛尔和每天服用2至15毫克哌唑嗪的联合方案。每次治疗方案改变后五到六个月分别评估其效果。在研究开始时以及每次改变后测定血脂和高密度脂蛋白浓度,并进行静脉葡萄糖耐量试验。在治疗方案从利尿剂改为哌唑嗪的组中,血清胆固醇和甘油三酯浓度分别显著下降了11%和42%,但在治疗方案从肼屈嗪改为哌唑嗪的组中,血脂或脂蛋白没有变化。治疗方案的改变对通过静脉葡萄糖耐量试验评估的血糖或胰岛素参数没有总体影响。然而,哌唑嗪与空腹血糖水平升高以及葡萄糖注射后胰岛素峰值降低有关,这两种都是剂量相关效应。数据表明,从利尿剂改为哌唑嗪治疗后,在较低胰岛素值时,葡萄糖周转率至少与之前一样好。在那些治疗方案从普萘洛尔改为每天50毫克阿替洛尔的患者中,血清甘油三酯浓度下降了约10%,而在治疗方案从每天100毫克阿替洛尔改为50毫克阿替洛尔的组中,血脂或脂蛋白没有变化。结果表明,每天50毫克阿替洛尔和哌唑嗪的联合方案比利尿剂和普萘洛尔联合治疗具有代谢优势。这种优势在高血压患者的长期治疗中可能很重要。