Jansson Sven-Olof, Malm Anders E, Lundström Torbjörn
AstraZeneca R&D, Pepparedsleden 1, 431 83, Mölndal, Sweden,
Drugs R D. 2014 Dec;14(4):325-32. doi: 10.1007/s40268-014-0073-5.
To compare the effects of bisoprolol and metoprolol CR/ZOK (metoprolol succinate controlled release) on systolic blood pressure (bpsys) over a 24-h period in an in silico model.
On the basis of the observed data from ambulatory blood pressure measurements (ABPM), a model with an appropriate distribution and correlation structure was derived for simulation of 24-h bpsys patterns during treatment with commonly studied doses, assumed to be equipotent, of bisoprolol and metoprolol CR/ZOK. Input into the simulations was aligned with the available data on the diurnal efficacy and pharmacology profiles of these substances. The validity of the model was tested in a bootstrap model.
The simulation model reproduced the observed data with high congruence (p = 1.0). The mean 24-h bpsys values did not significantly differ between the two simulated groups (estimated overall change in bpsys [∆bpsys] for metoprolol versus bisoprolol = 2.7 mmHg [95% confidence interval -0.3 to 5.7 mmHg]; p = 0.08). There were clear diurnal differences, with bisoprolol being more effective earlier and metoprolol CR/ZOK being more effective later in the 24-h day. A validity test with 100 repeated samples gave an overall mean group difference of 1.4 ± 3.59 mmHg (p = 0.63 relative to simulation).
In a robust model for the simulation of 24-h ABPM, comparisons between bisoprolol and metoprolol CR/ZOK indicate a comparable overall blood pressure-lowering effect but different diurnal patterns, consistent with the pharmacokinetics of the two drugs. This difference may be of clinical relevance, given the recognized diurnal pattern of cardiovascular events.
在计算机模拟模型中比较比索洛尔和美托洛尔控释片(琥珀酸美托洛尔控释片)对24小时收缩压(SBP)的影响。
基于动态血压测量(ABPM)的观察数据,推导了一个具有适当分布和相关结构的模型,用于模拟常用剂量(假定等效)的比索洛尔和美托洛尔控释片治疗期间的24小时SBP模式。模拟的输入与这些药物的昼夜疗效和药理学特征的现有数据一致。在自举模型中测试了该模型的有效性。
模拟模型高度一致地再现了观察数据(p = 1.0)。两个模拟组之间的24小时平均SBP值无显著差异(美托洛尔与比索洛尔的SBP估计总体变化[∆SBP] = 2.7 mmHg [95%置信区间 -0.3至5.7 mmHg];p = 0.08)。存在明显的昼夜差异,比索洛尔在24小时的早期更有效,美托洛尔控释片在后期更有效。100次重复样本的有效性测试得出总体平均组间差异为1.4 ± 3.59 mmHg(相对于模拟,p = 0.63)。
在一个用于模拟24小时ABPM的稳健模型中,比索洛尔和美托洛尔控释片之间的比较表明总体降压效果相当,但昼夜模式不同,这与两种药物的药代动力学一致。鉴于已认识到的心血管事件的昼夜模式,这种差异可能具有临床相关性。