Deger G
Am J Med. 1986 May 23;80(5B):82-5. doi: 10.1016/0002-9343(86)90858-2.
The effect of terazosin administration on serum lipid profiles was assessed in four multicenter, randomized, controlled, double-blind studies in which patients were treated for mild to moderate hypertension. Three studies were placebo-controlled, fixed-dose studies in which the dose of terazosin was gradually increased to a fixed level of 5, 10, or 20 mg once daily, and remained fixed for four weeks. The remaining study was a placebo-controlled, dose-titration study designed to compare the antihypertensive effects of once-daily administration of terazosin with those of twice-daily administration of prazosin. In this study, the dosage of medication was titrated until a satisfactory decrease in supine diastolic blood pressure was obtained, or until the maximum daily dosage (20 mg) was reached. When data from the three fixed-dose studies were pooled, analysis of fasting blood samples revealed that mean serum cholesterol and the low-density lipoprotein plus very-low-density lipoprotein cholesterol fraction were significantly (p less than or equal to 0.05) decreased during terazosin monotherapy (-5.4 mg/dl and -6.1 mg/dl, respectively) in comparison with placebo (-0.2 mg/dl and -1.0 mg/dl, respectively). Terazosin therapy was also associated with a significant within-group increase in the cholesterol ratio. In the dose-titration, comparative study, both terazosin- and prazosin-treated patients experienced significant within-group increases in the cholesterol ratio (1.8 and 2.3, respectively). Although changes in lipid parameters in the dose-titration comparative study were not significantly different between the three treatment groups, all changes in the tetrazosin and prazosin groups were in a beneficial direction, and were greater in magnitude than those observed in the placebo group. Observations from the four studies suggest that terazosin may exert a positive effect on the lipid profile.
在四项多中心、随机、对照、双盲研究中,评估了服用特拉唑嗪对血清脂质谱的影响,这些研究中的患者均接受轻度至中度高血压治疗。三项研究为安慰剂对照、固定剂量研究,其中特拉唑嗪剂量逐渐增加至每日一次5、10或20毫克的固定水平,并维持四周。其余一项研究为安慰剂对照、剂量滴定研究,旨在比较每日一次服用特拉唑嗪与每日两次服用哌唑嗪的降压效果。在这项研究中,药物剂量进行滴定,直至仰卧位舒张压令人满意地降低,或直至达到最大日剂量(20毫克)。将三项固定剂量研究的数据汇总后,对空腹血样的分析显示,与安慰剂(分别为-0.2毫克/分升和-1.0毫克/分升)相比,特拉唑嗪单药治疗期间(分别为-5.4毫克/分升和-6.1毫克/分升),平均血清胆固醇以及低密度脂蛋白加极低密度脂蛋白胆固醇组分显著降低(p小于或等于0.05)。特拉唑嗪治疗还与组内胆固醇比值显著升高相关。在剂量滴定比较研究中,特拉唑嗪和哌唑嗪治疗的患者组内胆固醇比值均显著升高(分别为1.8和2.3)。尽管剂量滴定比较研究中三个治疗组之间脂质参数的变化无显著差异,但特拉唑嗪组和哌唑嗪组的所有变化均朝着有益方向,且幅度大于安慰剂组。四项研究的观察结果表明,特拉唑嗪可能对脂质谱产生积极影响。