你所需要知道的异速结垢:理论基础、经验证据和在人类药理学中的应用的综合综述。

IF 4.6 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Clinical Pharmacokinetics Pub Date : 2025-02-01 Epub Date: 2024-12-07 DOI:10.1007/s40262-024-01444-6
Daan W van Valkengoed, Elke H J Krekels, Catherijne A J Knibbe
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引用次数: 0

摘要

缩放方法用于描述或预测儿童或肥胖人群从正常体重成人值的清除率。理论异速生长假设存在一个普遍的基于体重的比例关系。虽然异速生长理论存在很大争议,但在药理学数据分析和临床实践中得到了广泛的应用。当前综述的目的是:(1)增加药理学家对理论异速生长的理解,以更好地理解(隐含的)假设和(非)优势;(2)强调应用该方法时重要的方法学考虑。理论异速生长起源于Kleiber对哺乳动物基础代谢率和体重之间的比例指数为0.75的经验观察,后来引起了争论。韦斯特、布朗和恩奎斯特的数学框架为这个值提供了一个可能的解释。迄今为止,该框架的多个关键假设已被争议或反驳,并且越来越多的证据正在出现,反对存在一个通用异速指数。理论方法带来的易用性和通用性的承诺可能是它们受到如此强烈追捧和捍卫的原因。然而,生态学家建议,该理论应该从“牛顿方法”转向“达尔文方法”,在“牛顿方法”中,物理解释是寻求普遍规律的,可变性是次要的,在“达尔文方法”中,可变性被认为是最重要的,可以找到进化的解释。异速生长法应用于种内标度尚无科学依据,因此基于基础代谢率的标度原理应用于清除标度仍未得到证实。基于生理学的建模方法的最新见解强调了具有不同性质的药物和药物清除基础的生理变量之间的相互作用,这推动了药理学领域异速缩放指数的变异性。为了处理这种可变性,提出了对理论异速缩放的药物特异性或患者特异性适应,这引入了经验元素并降低了理论的普遍性。除了最年轻的个体(年龄≤5岁)之外,使用指数为0.75的异速缩放可能对儿科人群具有经验价值。然而,基于0.75异速尺度的模型的生物学解释和外推潜力在理论上是没有根据的,并且对于所有模型,该函数的经验应用的优点应该始终得到适当的模型验证程序的支持。在这方面,主要关注的不是异速生长指数的值,而是对个体清除率值和药物浓度的描述和预测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
All You Need to Know About Allometric Scaling: An Integrative Review on the Theoretical Basis, Empirical Evidence, and Application in Human Pharmacology.

Scaling approaches are used to describe or predict clearance for paediatric or obese populations from normal-weight adult values. Theoretical allometry assumes the existence of a universal bodyweight-based scaling relationship. Although theoretical allometry is highly disputed, it is commonly applied in pharmacological data analyses and clinical practice. The aim of the current review is to (1) increase pharmacologists' understanding of theoretical allometry to better understand the (implicit) assumptions and (dis)advantages and (2) highlight important methodological considerations with the application of this methodology. Theoretical allometry originated in an empirical, and later debated, observation by Kleiber of a scaling exponent of 0.75 between basal metabolic rate and body mass of mammals. The mathematical framework of West, Brown, and Enquist provides one possible explanation for this value. To date, multiple key assumptions of this framework have been disputed or disproven, and an increasing body of evidence is emerging against the existence of one universal allometric exponent. The promise of ease and universality of use that comes with theoretical approaches may be the reason they are so strongly sought after and defended. However, ecologists have suggested that the theory should move from a 'Newtonian approach', in which physical explanations are sought for a universal law and variability is of minor importance, to a 'Darwinian approach', in which variability is considered of primary importance for which evolutionary explanations can be found. No scientific support was found for the application of allometry for within-species scaling, so the application of basal metabolic rate-based scaling principles to clearance scaling remains unsubstantiated. Recent insights from physiologically based modelling approaches emphasise the interplay between drugs with different properties and physiological variables that underlie drug clearance, which drives the variability in the allometric scaling exponent in the field of pharmacology. To deal with this variability, drug-specific or patient-specific adaptations to theoretical allometric scaling are proposed, that introduce empiric elements and reduce the universality of the theory. The use of allometric scaling with an exponent of 0.75 may hold empirical merit for paediatric populations, except for the youngest individuals (aged ≤ 5 years). Nevertheless, biological interpretations and extrapolation potential attributed to models based on 0.75 allometric scaling are theoretically unfounded, and merits of the empirical application of this function should, as for all models, always be supported by appropriate model validation procedures. In this respect, it is not the value of the allometric exponent but the description and prediction of individual clearance values and drug concentrations that are of primary interest.

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来源期刊
CiteScore
8.80
自引率
4.40%
发文量
86
审稿时长
6-12 weeks
期刊介绍: Clinical Pharmacokinetics promotes the continuing development of clinical pharmacokinetics and pharmacodynamics for the improvement of drug therapy, and for furthering postgraduate education in clinical pharmacology and therapeutics. Pharmacokinetics, the study of drug disposition in the body, is an integral part of drug development and rational use. Knowledge and application of pharmacokinetic principles leads to accelerated drug development, cost effective drug use and a reduced frequency of adverse effects and drug interactions.
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