Repository Describing an Aging Population to Inform Physiologically Based Pharmacokinetic Models Considering Anatomical, Physiological, and Biological Age-Dependent Changes

被引:59
作者
Stader, Felix [1 ,2 ,3 ,4 ]
Siccardi, Marco [5 ]
Battegay, Manuel [1 ,2 ,4 ]
Kinvig, Hannah [5 ]
Penny, Melissa A. [3 ,4 ]
Marzolini, Catia [1 ,2 ,4 ]
机构
[1] Univ Hosp Basel, Div Infect Dis & Hosp Epidemiol, Dept Med, Basel, Switzerland
[2] Univ Hosp Basel, Div Infect Dis & Hosp Epidemiol, Dept Clin Res, Basel, Switzerland
[3] Swiss Trop & Publ Hlth Inst, Dept Epidemiol & Publ Hlth, Infect Dis Modelling Unit, Basel, Switzerland
[4] Univ Basel, Basel, Switzerland
[5] Univ Liverpool, Inst Translat Med, Dept Mol & Clin Pharmacol, Liverpool, Merseyside, England
关键词
CEREBRAL-BLOOD-FLOW; NORMAL ORGAN WEIGHTS; TOTAL-BODY WATER; GLOMERULAR-FILTRATION-RATE; ALPHA-1 ACID GLYCOPROTEIN; METABOLIC-DRUG CLEARANCE; HUMAN MICROSOMAL PROTEIN; HUMAN LIVER-MICROSOMES; CROSS-SECTIONAL SURVEY; SKELETAL-MUSCLE MASS;
D O I
10.1007/s40262-018-0709-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BackgroundAging is characterized by anatomical, physiological, and biological changes that can impact drug kinetics. The elderly are often excluded from clinical trials and knowledge about drug kinetics and drug-drug interaction magnitudes is sparse. Physiologically based pharmacokinetic modeling can overcome this clinical limitation but detailed descriptions of the population characteristics are essential to adequately inform models.ObjectiveThe objective of this study was to develop and verify a population database for aging Caucasians considering anatomical, physiological, and biological system parameters required to inform a physiologically based pharmacokinetic model that included population variability.MethodsA structured literature search was performed to analyze age-dependent changes of system parameters. All collated data were carefully analyzed, and descriptive mathematical equations were derived.ResultsA total of 362 studies were found of which 318 studies were included in the analysis as they reported rich data for anthropometric parameters and specific organs (e.g., liver). Continuous functions could be derived for most system parameters describing a Caucasian population from 20 to 99years of age with variability. Areas with sparse data were identified such as tissue composition, but knowledge gaps were filled with plausible qualified assumptions. The developed population was implemented in Matlab((R)) and estimated system parameters from 1000 virtual individuals were in accordance with independent observed data showing the robustness of the developed population.ConclusionsThe developed repository for aging subjects provides a singular specific source for key system parameters needed for physiologically based pharmacokinetic modeling and can in turn be used to investigate drug kinetics and drug-drug interaction magnitudes in the elderly.
引用
收藏
页码:483 / 501
页数:19
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