Chen M F, Yang C Y, Chen W J, Lee C M, Wu C C, Liau C S, Lee Y T
Department of Internal Medicin (Cardiology), National Taiwan University Hospital, Taipei.
Cardiovasc Drugs Ther. 1995 Jun;9(3):401-6. doi: 10.1007/BF00879028.
The efficacy and tolerability of controlled-release metoprolol (metoprolol CR/ZOK), 100-200 mg, and atenolol, 50-100 mg, once daily was compared in Chinese patients with mild to moderate essential hypertension. The study was of a randomized, double-blind, two-way crossover design. The active treatment periods lasted 4 weeks each and were preceded by a 4-week placebo run-in period. The two double-blind phases were separated by a 2-week washout period on placebo. Blood pressures and heart rates were measured at rest in each 2-week visit and during exercise at the end of each treatment period. Twenty-four patients (M/F = 14/10) were valid for efficacy analysis. Their ages ranged from 39 to 68, with a mean of 53.5 years. The rest supine blood pressure and heart rate before active treatment was 160 +/- 15/106 +/- 6 mmHg and 75 +/- 14 beats/min (mean +/- SD), respectively. A responder was defined as exhibiting a supine diastolic blood pressure < or = 90 mmHg or a supine diastolic blood pressure reduction of at least 10% of the baseline level. Both agents had high response rate: 88% and 92% of all patients responded to metoprolol CR/ZOK and atenolol, respectively. Both active treatments considerably reduced resting systolic and diastolic blood pressures and heart rates as compared with baseline (p < 0.001), respectively. With controlled-release metoprolol, a more pronounced beta 1 blockade was obtained than with atenolol, which was expressed as a significant reduction in exercise-induced heart rate at the highest comparable workload compared with placebo (p < 0.05). These findings are compatible with those reported from western populations.
对100 - 200毫克控释美托洛尔(美托洛尔CR/ZOK)和50 - 100毫克阿替洛尔,每日一次给药,在中国轻至中度原发性高血压患者中比较二者的疗效和耐受性。该研究采用随机、双盲、双向交叉设计。每个积极治疗期持续4周,之前有4周的安慰剂导入期。两个双盲阶段之间有2周的安慰剂洗脱期。在每2周的访视时测量静息血压和心率,并在每个治疗期结束时测量运动时的血压和心率。24例患者(男/女 = 14/10)纳入疗效分析。他们的年龄在39至68岁之间,平均年龄为53.5岁。积极治疗前静息仰卧位血压和心率分别为160±15/106±6 mmHg和75±14次/分钟(均值±标准差)。反应者定义为仰卧位舒张压≤90 mmHg或仰卧位舒张压较基线水平降低至少10%。两种药物的有效率均较高:所有患者中分别有88%和92%对美托洛尔CR/ZOK和阿替洛尔有反应。与基线相比,两种积极治疗均显著降低了静息收缩压、舒张压和心率(p < 0.001)。与阿替洛尔相比,控释美托洛尔获得了更显著的β1受体阻滞作用,这表现为在最高可比工作量下与安慰剂相比运动诱发的心率显著降低(p < 0.05)。这些发现与西方人群报道的结果一致。