Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
Hypertens Res. 2012 Nov;35(11):1080-6. doi: 10.1038/hr.2012.110. Epub 2012 Jul 12.
The objective of this study is to examine the effects of thiazide diuretics, plus medium-dose losartan versus maximal-dose angiotensin II receptor blockers (ARBs) on blood pressure (BP) in Japanese patients with uncontrolled hypertension despite the use of medium-dose ARBs. Hypertensive patients in whom BP was inadequately controlled by treatment with medium-dose ARBs alone or with calcium-channel blockers were enrolled. Patients were randomly assigned to a fixed-dose combination of 50 mg per day losartan and 12.5 mg per day hydrochlorothiazide (HCTZ; n=98), or to a maximal dose of current ARBs (n=95). The reduction in office BP from baseline was significantly larger in the losartan/HCTZ group than in the maximal-dose ARB group (systolic BP -22.7±13.7 vs. -11.7±13.0 mm Hg, diastolic BP -9.6±10.9 vs. -4.5±11.0 mm Hg; P<0.01, respectively). The proportion of patients in whom the therapeutic target BP was achieved was greater in the losartan/HCTZ group than in the maximal-dose ARB group (59.2 vs. 26.3%; P<0.001). Both early-morning and evening BP were controlled more effectively over 1 year of treatment in the losartan/HCTZ group than in the maximal-dose ARB group (the mean BP difference between the groups, early-morning: 5.6 mm Hg (P=0.001), evening: 3.8 mm Hg (P=0.049)). Adverse changes in serum potassium and uric acid were observed in the losartan/HCTZ group; however, both changes were very slight, and the values were still within the normal range. The concomitant usage of losartan and HCTZ had no influence on glucose metabolism and lipid profiles. Declines in plasma N-terminal pro-brain natriuretic peptide levels and urinary albumin excretion were observed in the losartan/HCTZ group, but not in the maximal-dose ARB group. Switching from medium-dose ARBs to losartan plus HCTZ reduced both office and home BP efficiently in patients with uncontrolled hypertension.
本研究旨在探讨噻嗪类利尿剂加中等剂量氯沙坦与最大剂量血管紧张素 II 受体阻滞剂(ARB)对使用中等剂量 ARB 仍未控制的高血压患者血压(BP)的影响。入组患者为单独使用中等剂量 ARB 或钙通道阻滞剂治疗血压控制不佳的高血压患者。患者被随机分配至固定剂量组合(每天 50mg 氯沙坦和 12.5mg 氢氯噻嗪[HCTZ];n=98)或当前最大剂量 ARB(n=95)。与最大剂量 ARB 组相比,氯沙坦/HCTZ 组的诊室 BP 降低更显著(收缩压-22.7±13.7 对-11.7±13.0mmHg,舒张压-9.6±10.9 对-4.5±11.0mmHg;P<0.01)。氯沙坦/HCTZ 组达到治疗目标 BP 的患者比例高于最大剂量 ARB 组(59.2%对 26.3%;P<0.001)。与最大剂量 ARB 组相比,氯沙坦/HCTZ 组在 1 年治疗期间清晨和傍晚 BP 控制更有效(两组间平均 BP 差值,清晨:5.6mmHg(P=0.001),傍晚:3.8mmHg(P=0.049))。氯沙坦/HCTZ 组观察到血清钾和尿酸的不良变化;然而,这些变化非常轻微,并且值仍在正常范围内。氯沙坦和 HCTZ 的同时使用对血糖代谢和血脂谱没有影响。氯沙坦/HCTZ 组观察到血浆 N 末端脑利钠肽前体水平和尿白蛋白排泄的下降,但最大剂量 ARB 组没有。从中等剂量 ARB 转换为氯沙坦加 HCTZ 可有效降低未控制高血压患者的诊室和家庭 BP。