Arch Intern Med. 1981 Mar;141(4):482-6.
A randomized, double-blind, multicenter study comparing amiloride hydrochloride, amiloride hydrochloride plus hydrochlorothiazide, and hydrochlorothiazide was conducted in 179 patients with mild to moderate essential hypertension (diastolic pressure, 95 to 115 mm Hg). After 12 weeks of treatment, significant reductions in pressure were observed for all three treatment groups. Systolic pressure reduction was greatest for amiloride plus hydrochlorothiazide. Baseline vs 12-week average supine pressures were 153/101 vs 139/93 mm Hg for amiloride, 160/100 vs 137/90 mm Hg for amiloride plus hydrochlorothiazide, and 154/101 vs 134/89 mm Hg for hydrochlorothiazide. Baseline vs treatment mean serum potassium levels were 4.24 vs 4.47 mEq/L for amiloride, 4.24 vs 3.86 mEq/L for the combination, and 4.15 vs 3.56 mEq/L for hydrochlorothiazide. The changes in serum potassium level from the baseline for amiloride plus hydrochlorothiazide were significantly different from those for hydrochlorothiazide throughout the study (except for week 6). All drugs were well tolerated, and no drug-related toxic reaction was detected. This study demonstrates the efficacy of amiloride and amiloride plus hydrochlorothiazide as diuretic antihypertensive potassium-conserving agents.
一项随机、双盲、多中心研究对179例轻度至中度原发性高血压患者(舒张压95至115毫米汞柱)进行了比较,治疗药物分别为盐酸阿米洛利、盐酸阿米洛利加氢氯噻嗪和氢氯噻嗪。治疗12周后,所有三个治疗组的血压均显著降低。盐酸阿米洛利加氢氯噻嗪组的收缩压降低幅度最大。盐酸阿米洛利组基线仰卧位血压与12周平均仰卧位血压分别为153/101与139/93毫米汞柱,盐酸阿米洛利加氢氯噻嗪组为160/100与137/90毫米汞柱,氢氯噻嗪组为154/101与134/89毫米汞柱。盐酸阿米洛利组基线与治疗后平均血清钾水平分别为4.24与4.47毫当量/升,联合用药组为4.24与3.86毫当量/升,氢氯噻嗪组为4.15与3.56毫当量/升。在整个研究过程中(第6周除外),盐酸阿米洛利加氢氯噻嗪组血清钾水平相对于基线的变化与氢氯噻嗪组显著不同。所有药物耐受性良好,未检测到与药物相关的毒性反应。本研究证明了盐酸阿米洛利以及盐酸阿米洛利加氢氯噻嗪作为利尿性保钾抗高血压药物的疗效。