Pool J L, Cushman W C, Saini R K, Nwachuku C E, Battikha J P
Section on Hypertension and Clinical Pharmacology, Baylor College of Medicine, Houston, Texas, USA.
Am J Hypertens. 1997 Jan;10(1):117-23. doi: 10.1016/s0895-7061(96)00323-8.
The combination of angiotensin converting enzyme (ACE) inhibitor and thiazide diuretic has advantages over monotherapy for the treatment of hypertension. Previous study designs have often been inadequate to demonstrate the details of interactions between these antihypertensive agents. This study used a modified 4 x 4 factorial randomized, double-blind, placebo-controlled, parallel group design to study the efficacy of 17 different doses of fosinopril (Fos), a phosphinic acid derived ACE inhibitor, and hydrochlorothiazide (HCTZ) in 550 patients with mild to moderate hypertension. Data from these variables were fit to quadratic response surface models (QRSM) using polynomial functions in the doses of the two components. Using QRSM, seated systolic (SeSBP) and diastolic blood pressure (SeDBP) responses at 8 weeks were predicted for actual doses and interpolated for intermediate doses not studied. Fos and HCTZ alone and in combination produced a dose-related reduction in SeSBP and SeDBP. Using 10 mg Fos + 12.5 mg HCTZ reduced the adjusted mean SeDBP 6.3 mm Hg and 20 mg Fos + 12.5 mg HCTZ lowered the same measure 9.1 mm Hg. Coadministration of Fos and HCTZ produced an additive antihypertensive effect. This study of combination agents for hypertension using a factorial design with QRSM accurately predicts dose responses and is a valuable clinical trial methodology.
血管紧张素转换酶(ACE)抑制剂与噻嗪类利尿剂联合使用在治疗高血压方面比单一疗法具有优势。以往的研究设计往往不足以阐明这些抗高血压药物之间相互作用的细节。本研究采用改良的4×4析因随机、双盲、安慰剂对照、平行组设计,研究17种不同剂量的福辛普利(Fos,一种次膦酸衍生的ACE抑制剂)和氢氯噻嗪(HCTZ)对550例轻至中度高血压患者的疗效。使用这两种成分剂量的多项式函数,将这些变量的数据拟合到二次响应曲面模型(QRSM)中。使用QRSM,预测了8周时实际剂量的坐位收缩压(SeSBP)和舒张压(SeDBP)反应,并对未研究的中间剂量进行了内插。Fos和HCTZ单独使用及联合使用均使SeSBP和SeDBP出现剂量相关的降低。使用10 mg Fos + 12.5 mg HCTZ可使调整后的平均SeDBP降低6.3 mmHg,20 mg Fos + 12.5 mg HCTZ可使同一指标降低9.1 mmHg。Fos和HCTZ联合给药产生了相加的降压作用。这项使用析因设计和QRSM对高血压联合用药的研究准确地预测了剂量反应,是一种有价值的临床试验方法。