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Diverse Data Sets Can Yield Reliable Information through Mechanistic Modeling: Salicylic Acid Clearance

机译:多样化的数据集可以通过机械建模获得可靠的信息:水杨酸清除率

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摘要

This is a practical example of a powerful research strategy: putting together data from studies covering a diversity of conditions can yield a scientifically sound grasp of the phenomenon when the individual observations failed to provide definitive understanding. The rationale is that defining a realistic, quantitative, explanatory hypothesis for the whole set of studies, brings about a “consilience” of the often competing hypotheses considered for individual data sets. An internally consistent conjecture linking multiple data sets simultaneously provides stronger evidence on the characteristics of a system than does analysis of individual data sets limited to narrow ranges of conditions. Our example examines three very different data sets on the clearance of salicylic acid from humans: a high concentration set from aspirin overdoses; a set with medium concentrations from a research study on the influences of the route of administration and of sex on the clearance kinetics, and a set on low dose aspirin for cardiovascular health. Three models were tested: (1) a first order reaction, (2) a Michaelis-Menten (M-M) approach, and (3) an enzyme kinetic model with forward and backward reactions. The reaction rates found from model 1 were distinctly different for the three data sets, having no commonality. The M-M model 2 fitted each of the three data sets but gave a reliable estimates of the Michaelis constant only for the medium level data (Km = 24±5.4 mg/L); analyzing the three data sets together with model 2 gave Km = 18±2.6 mg/L. (Estimating parameters using larger numbers of data points in an optimization increases the degrees of freedom, constraining the range of the estimates). Using the enzyme kinetic model (3) increased the number of free parameters but nevertheless improved the goodness of fit to the combined data sets, giving tighter constraints, and a lower estimated Km = 14.6±2.9 mg/L, demonstrating that fitting diverse data sets with a single model improves confidence in the results. This modeling effort is also an example of reproducible science available at
机译:这是一个强有力的研究策略的实际例子:当各个观察结果未能提供确定的理解时,将涵盖各种条件的研究数据汇总在一起,就可以对现象进行科学的把握。基本原理是,为整个研究定义一个现实的,定量的,解释性的假设,可以为各个数据集考虑经常相互竞争的假设,使其具有“一致性”。一个内部一致的猜想同时链接了多个数据集,比对单个数据集的分析仅限于狭窄的条件范围,该推测更能证明系统的特征。我们的示例研究了关于水杨酸从人体内清除的三个非常不同的数据集:阿司匹林过量导致的高浓度数据集;一组来自中等浓度的药物,该药物来自有关给药途径和性别对清除动力学影响的研究,另一组涉及低剂量阿司匹林对心血管健康的影响。测试了三个模型:(1)一阶反应;(2)Michaelis-Menten(M-M)方法;(3)具有正向和反向反应的酶动力学模型。对于三个数据集,从模型1发现的反应速率明显不同,没有共同点。 M-M模型2拟合了三个数据集的每一个,但仅对中等水平的数据(Km = 24±5.4 mg / L)给出了米氏常数的可靠估计;与模型2一起分析这三个数据集,得出Km = 18±2.6 mg / L。 (在优化中使用大量数据点来估计参数会增加自由度,从而限制了估计范围)。使用酶动力学模型(3)可以增加自由参数的数量,但仍提高了对组合数据集的拟合优度,给出了更严格的约束条件,并降低了估计Km = 14.6±2.9 mg / L,表明了对各种数据集的拟合单一模型可以提高对结果的信心。这种建模工作也是可再生科学的一个示例,可从以下网站获得

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