McCrea J B, Lo M W, Tomasko L, Lin C C, Hsieh J Y, Capra N L, Goldberg M R
Department of Clinical Pharmacology, Merck Research Laboratories, West Point, Pennsylvania 19486, USA.
J Clin Pharmacol. 1995 Dec;35(12):1200-6. doi: 10.1002/j.1552-4604.1995.tb04047.x.
To support the use of a combination of losartan, a highly specific and selective AT1 angiotensin II receptor antagonist, and hydrochlorothiazide for treatment of hypertension, a pharmacokinetic drug interaction study was conducted. In this open-label, randomized, three-period, crossover study, patients with mild to moderate hypertension received a 12.5-mg tablet of hydrochlorothiazide, a 50-mg losartan tablet, or a combination tablet of 12.5 mg of hydrochlorothiazide and 50 mg of losartan for 7 days. Twelve patients (age range, 35-55 years; mean age, 44 years) were allocated to treatment. Drug interactions were evaluated by comparing the 24-hour area under the concentration-time curve (AUC24) for losartan and its active metabolite, E-3174, when losartan (50 mg) was given alone or in combination with 12.5 mg hydrochlorothiazide. The urinary recovery over the 24-hour period of hydrochlorothiazide was compared for hydrochlorothiazide (12.5 mg) given alone or in combination with 50 mg losartan. A clinically significant interaction was defined as a treatment difference of more than 35%. There was no evidence of a clinically significant effect of hydrochlorothiazide on the pharmacokinetics of losartan or E-3174, as the geometric mean AUC24 ratio (90% confidence interval [CI]) was 1.02 (0.95, 1.09) for losartan and 1.02 (0.96, 1.09) for E-3174. Based on urinary recovery over a 24-hour period of hydrochlorothiazide, losartan did not affect the pharmacokinetics of hydrochlorothiazide, as the geometric mean ratio of urinary hydrochlorothiazide recovery (90% CI) was 0.898 (0.79, 1.20). There was a minor (17%) decrease in the AUC24 of hydrochlorothiazide after administration of the combination tablet. Coadministration of hydrochlorothiazide and losartan was well tolerated.
为支持使用高特异性和选择性的 AT1 血管紧张素 II 受体拮抗剂氯沙坦与氢氯噻嗪联合治疗高血压,进行了一项药代动力学药物相互作用研究。在这项开放标签、随机、三周期、交叉研究中,轻度至中度高血压患者接受 12.5 毫克氢氯噻嗪片、50 毫克氯沙坦片或 12.5 毫克氢氯噻嗪与 50 毫克氯沙坦的复方片剂治疗 7 天。12 名患者(年龄范围 35 - 55 岁;平均年龄 44 岁)被分配接受治疗。通过比较氯沙坦(50 毫克)单独给药或与 12.5 毫克氢氯噻嗪联合给药时氯沙坦及其活性代谢物 E - 3174 的 24 小时浓度 - 时间曲线下面积(AUC24)来评估药物相互作用。比较单独给予氢氯噻嗪(12.5 毫克)或与 50 毫克氯沙坦联合给药时氢氯噻嗪在 24 小时内的尿回收率。具有临床意义的相互作用定义为治疗差异超过 35%。没有证据表明氢氯噻嗪对氯沙坦或 E - 3174 的药代动力学有临床显著影响,因为氯沙坦的几何平均 AUC24 比值(90%置信区间[CI])为 1.02(0.95,1.09),E - 3174 为 1.02(0.96,1.09)。基于氢氯噻嗪 24 小时内的尿回收率,氯沙坦不影响氢氯噻嗪的药代动力学,因为氢氯噻嗪尿回收率的几何平均比值(90%CI)为 0.898(0.79,1.20)。服用复方片剂后氢氯噻嗪的 AUC24 有轻微(17%)下降。氢氯噻嗪和氯沙坦联合给药耐受性良好。