Townsend R, Haggert B, Liss C, Edelman J M
Department of Medicine, University of Pennsylvania, Philadelphia, USA.
Clin Ther. 1995 Sep-Oct;17(5):911-23. doi: 10.1016/0149-2918(95)80069-7.
The antihypertensive effects and the tolerability of losartan and enalapril given alone or in combination with hydrochlorothiazide (HCTZ) were compared in a multicenter, double-blind, randomized, parallel-group, 16-week clinical trial. The study consisted of a 4-week placebo washout phase and a 12-week active treatment phase. Patients with mild-to-moderate, uncomplicated essential hypertension were considered for participation in the study. To enter the treatment phase of the study, a mean sitting diastolic blood pressure (SiDBP) > or = 95 and < or = 115 mm Hg was required. Patients received either 50-mg losartan once daily or 5-mg enalapril once daily at randomization. The dose of enalapril could be titrated to 10 mg after 4 weeks and 25 mg of HCTZ could be added after 8 weeks, based on measurements of SiDBP at clinic visits. The dose of losartan remained at 50 mg; 12.5 mg of HCTZ could be added after 8 weeks. Changes in the treatment regimen at each step were required if SiDBP remained > or = mm Hg. Doses of the diuretic were chosen based on commercially available forms of the test agents in combination with HCTZ. Trough blood pressure, heart rate, and safety parameters were measured at 4-week intervals during the treatment phase of the study. Significant reductions in mean SiDBP and mean sitting systolic blood pressure (SiSBP) were achieved at all time points (4, 8, and 12 weeks) with both treatments. No significant differences between treatment groups for mean changes in SiDBP or SiSBP were observed overall. At study end, patients receiving the losartan regimen had a mean reduction in SiDBP of 10.3 mm Hg, whereas patients in the enalapril regimen had a mean reduction of 9.8 mm Hg. Likewise, the percentage of patients reaching goal blood pressure reduction was not significantly different between groups. The mean reduction in SiDBP-- but not SiSBP--in black patients was slightly greater in the losartan group than in the enalapril group (SiDBP, 10.0 mm Hg losartan vs 8.0 mm Hg enalapril; P = 0.02). Similarly, losartan patients aged 65 years and older had a slightly greater decrease in SiDBP than comparable enalapril patients (12.7 mm Hg vs 8.7 mm Hg; P = 0.03). The importance of these differences between subgroups must be clarified by additional studies. Overall, both treatments were well tolerated. A regimen of losartan alone or in combination with HCTZ was effective in treating patients with essential hypertension and was comparable to a regimen of enalapril alone or in combination with HCTZ. However, treatment with losartan was associated with a lower incidence of cough.
在一项多中心、双盲、随机、平行组、为期16周的临床试验中,比较了单独使用氯沙坦和依那普利,或二者与氢氯噻嗪(HCTZ)联合使用时的降压效果及耐受性。该研究包括为期4周的安慰剂洗脱期和为期12周的积极治疗期。纳入轻度至中度、无并发症的原发性高血压患者参与研究。要进入研究的治疗阶段,要求平均坐位舒张压(SiDBP)≥95且≤115 mmHg。患者在随机分组时,随机接受每日一次50 mg氯沙坦或每日一次5 mg依那普利治疗。根据门诊就诊时SiDBP的测量结果,依那普利的剂量在4周后可滴定至10 mg,8周后可加用25 mg HCTZ。氯沙坦的剂量维持在50 mg;8周后可加用12.5 mg HCTZ。如果SiDBP仍≥ mmHg,则需要在每个步骤改变治疗方案。利尿剂的剂量根据与HCTZ联合使用的受试药物的市售剂型选择。在研究的治疗阶段,每隔4周测量一次谷值血压、心率和安全参数。两种治疗方法在所有时间点(4周、8周和12周)均使平均SiDBP和平均坐位收缩压(SiSBP)显著降低。总体而言,各治疗组之间SiDBP或SiSBP的平均变化无显著差异。在研究结束时,接受氯沙坦治疗方案的患者SiDBP平均降低10.3 mmHg,而接受依那普利治疗方案的患者平均降低9.8 mmHg。同样,两组中达到目标血压降低的患者百分比无显著差异。氯沙坦组黑人患者的SiDBP平均降低幅度略大于依那普利组(氯沙坦组SiDBP为10.0 mmHg,依那普利组为8.0 mmHg;P = 0.02)。同样,65岁及以上的氯沙坦患者SiDBP的降低幅度略大于依那普利组的相应患者(12.7 mmHg对8.7 mmHg;P = 0.03)。这些亚组间差异的重要性必须通过进一步研究加以阐明。总体而言,两种治疗方法耐受性良好。单独使用氯沙坦或与HCTZ联合使用的治疗方案对原发性高血压患者有效,且与单独使用依那普利或与HCTZ联合使用的治疗方案相当。然而氯沙坦治疗引起咳嗽的发生率较低。