Hoffbrand B I, Earle K A, Nievel J G, Restrick L J, Simmonds N J
Department of Medicine, Whittington Hospital, London, UK.
Postgrad Med J. 1993 Feb;69(808):117-20. doi: 10.1136/pgmj.69.808.117.
Twenty-eight patients (11 Caucasian, 17 black) whose blood pressure was more than 160/96 mmHg after 4 weeks on placebo added to atenolol 100 mg/day were randomly given, in addition, nisoldipine 10 mg or nifedipine 20 mg each twice a day for 8 weeks in a double-blind cross-over study. There was a statistically significant (P < 0.001) fall in blood pressure with no change in heart rate, both supine and erect, on both drugs. There were no significant differences between nisoldipine and nifedipine. Adverse effects were recorded in 15%, 17% and 35% of the patients available for safety comparison for placebo, nisoldipine and nifedipine, respectively. There were no significant differences between the black and Caucasian patients in blood pressure responses, although the study had only a low power to detect these. However, the fasting serum triglyceride levels at the end of both calcium antagonist treatment periods were highly significantly lower in the black patients compared with the Caucasian patients. Nisoldipine, which has a higher coronary vascular selectivity and less negative inotropism than nifedipine, is as effective and as well tolerated as nifedipine in patients whose hypertension is inadequately controlled on atenolol. It may have a special role in hypertensive patients with impaired left ventricular function.
在一项双盲交叉研究中,28名患者(11名白种人,17名黑人)在服用每天100毫克阿替洛尔并加用安慰剂4周后血压仍高于160/96毫米汞柱,随后被随机给予尼索地平10毫克或硝苯地平20毫克,均每日两次,持续8周。两种药物均使仰卧位和直立位血压显著下降(P < 0.001),心率无变化。尼索地平和硝苯地平之间无显著差异。安慰剂、尼索地平、硝苯地平安全性可比的患者中,不良反应发生率分别为15%、17%和35%。黑种人和白种人患者的血压反应无显著差异,尽管该研究检测这些差异的效能较低。然而,与白种人患者相比,黑人患者在两个钙拮抗剂治疗期结束时的空腹血清甘油三酯水平显著更低。尼索地平比硝苯地平具有更高的冠脉血管选择性和更低的负性肌力作用,在阿替洛尔治疗血压控制不佳的患者中,其疗效和耐受性与硝苯地平相当。它可能在左心室功能受损的高血压患者中具有特殊作用。