Division of Cardiology, Department of Internal Medicine, College of Medicine, Seoul National University, Seoul, Korea.
Korean Circ J. 2009 Apr;39(4):151-6. doi: 10.4070/kcj.2009.39.4.151. Epub 2009 Apr 28.
The antihypertensive efficacy and tolerability of losartan (LST) in fixed combination with hydrochlorothiazide (HCTZ) has not been compared to those of amlodipine monotherapy in Asians. This is an important comparison to draw, because Asians have been suggested to respond more favorably to calcium channel blockers and less favorably to angiotensin-converting enzyme inhibitors in comparison to Westerners. We sought to compare these two regimens in Korean patients with mild to moderate hypertension.
174 patients were randomized to receive LST 50 mg once daily, which could be titrated to LST/HCTZ 50/12.5 mg at 4 weeks, followed by 100/25 mg at 8 weeks; or to receive amlodipine besylate 2.5 mg once daily, which could be titrated to 5 mg at 4 weeks, followed by 10 mg at 8 weeks to achieve diastolic blood pressure <90 mmHg.
At 12 weeks, the differences between the LST/HCTZ and amlodipine groups with regard to diastolic and systolic blood pressure were 1.2 mmHg (95% confidence interval: -1.1 to 3.4) and -0.5 mmHg (95% confidence interval: -4.3 to 3.4), respectively. The rates of achieving systolic blood pressure <140 mmHg were 66.7% in the LST/HCTZ group and 75.9% in the amlodipine group (p=0.20). The rates of drug-related adverse events were 15.6% in the LST/HCTZ group and 11.9% in the amlodipine group (p=0.49).
The two regimens, with a relatively higher dose of LST/HCTZ compared to that required in Westerners, produced equivalent blood pressure reduction and were comparably well tolerated in Korean patients with mild to moderate hypertension.
与氨氯地平单药治疗相比,氯沙坦(LST)与氢氯噻嗪(HCTZ)固定剂量联合的降压疗效和耐受性尚未在亚洲人群中进行比较。这是一个重要的比较,因为与西方人相比,亚洲人被认为对钙通道阻滞剂的反应更好,而对血管紧张素转换酶抑制剂的反应较差。我们试图在韩国轻中度高血压患者中比较这两种方案。
174 名患者被随机分配接受 LST 50 mg 每日一次,可在 4 周时滴定至 LST/HCTZ 50/12.5 mg,然后在 8 周时滴定至 100/25 mg;或接受苯磺酸氨氯地平 2.5 mg 每日一次,可在 4 周时滴定至 5 mg,然后在 8 周时滴定至 10 mg,以达到舒张压<90mmHg。
在 12 周时,LST/HCTZ 组与氨氯地平组之间舒张压和收缩压的差异分别为 1.2mmHg(95%置信区间:-1.1 至 3.4)和-0.5mmHg(95%置信区间:-4.3 至 3.4)。收缩压<140mmHg 的达标率分别为 LST/HCTZ 组 66.7%和氨氯地平组 75.9%(p=0.20)。药物相关不良反应发生率分别为 LST/HCTZ 组 15.6%和氨氯地平组 11.9%(p=0.49)。
与西方人所需剂量相比,LST/HCTZ 剂量较高的两种方案在韩国轻中度高血压患者中产生了等效的降压效果,且耐受性相当。