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琥珀酸美托洛尔与比索洛尔24小时收缩压的计算机模拟比较

In Silico comparison between metoprolol succinate and bisoprolol on 24-hour systolic blood pressures.

作者信息

Jansson Sven-Olof, Malm Anders E, Lundström Torbjörn

机构信息

AstraZeneca R&D, Pepparedsleden 1, 431 83, Mölndal, Sweden,

出版信息

Drugs R D. 2014 Dec;14(4):325-32. doi: 10.1007/s40268-014-0073-5.

Abstract

OBJECTIVE

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.

METHODS

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.

RESULTS

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).

CONCLUSION

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.

摘要

目的

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。

方法

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。

结果

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)。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18a6/4391103/e9975984a1c4/40268_2014_73_Fig1_HTML.jpg

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