Antihypertensive efficacy of zofenopril compared with atenolol in patients with mild to moderate hypertension.

Peter Nilsson
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引用次数: 19

Abstract

Two first-line antihypertensive therapies for initiating treatment in hypertension were compared, the angiotensin-converting enzyme inhibitor (ACEI) zofenopril and the beta-blocker atenolol. The study was multi-centre and double-blind, and included 304 middle-aged to elderly patients with mild to moderate hypertension who were randomized to receive either zofenopril 30-60 mg once daily (od) or atenolol 50-100 mg od for 4 weeks with the possibility to an up-titration in non-responding patients. The higher dose level was then administered until 12 weeks after randomization. Blood pressures (BPs) were substantially reduced by either treatment, but after 4 weeks, the systolic and diastolic BP reductions were significantly greater (p < 0.05) with zofenopril (-15.6/-13.5 mmHg) compared with atenolol (-13.1/-11.8 mmHg). After 12 weeks and the possibility of dose up-titration, BP differences between treatments were no longer significant. However, control rates (sitting diastolic BP < 90 mmHg) for zofenopril remained significantly higher compared with atenolol. The number of subjects with adverse drug reactions possibly or probably related to the study medication was 14 (9.1%) in the zofenopril group and 30 (20.8%) in the atenolol group (p = 0.008). It is concluded that zofenopril as well as atenolol induces substantial reductions of diastolic BP in middle-aged to elderly patients with hypertension. However, the control rate when initiating antihypertensive therapy with zofenopril is higher than that for atenolol.

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唑非诺普利与阿替洛尔在轻中度高血压患者中的降压疗效比较。
比较了血管紧张素转换酶抑制剂(ACEI)佐非诺普利和β受体阻滞剂阿替洛尔两种用于高血压起始治疗的一线降压药物。该研究为多中心双盲研究,纳入304名中老年轻中度高血压患者,随机接受左非诺普利30- 60mg每日一次(od)或阿替洛尔50- 100mg每日一次(od),持续4周,无反应患者可能会增加剂量。然后给予较高剂量水平,直到随机分组后12周。两种治疗均显著降低血压(BP),但4周后,与阿替洛尔(-13.1/-11.8 mmHg)相比,唑非普利(-15.6/-13.5 mmHg)的收缩压和舒张压降低幅度显著大于阿替洛尔(-13.1/-11.8 mmHg) (p < 0.05)。12周后,可能的剂量增加,治疗之间的血压差异不再显著。然而,与阿替洛尔相比,唑非普利的控制率(舒张压< 90mmhg)仍然显著高于阿替洛尔。发生可能或可能与研究药物有关的药物不良反应的受试者,唑非普利组为14人(9.1%),阿替洛尔组为30人(20.8%)(p = 0.008)。由此可见,佐非普利和阿替洛尔可显著降低中老年高血压患者的舒张压。然而,当开始使用唑非普利抗高血压治疗时,控制率高于阿替洛尔。
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