A Bayesian Approach for Population Pharmacokinetic Modeling of Alcohol in Japanese Individuals

Background: Blood alcohol concentration data that were previously obtained from 34 healthy Japanese subjects with limited sampling times were reanalyzed. Characteristics of the data were that the concentrations were obtained from only the early part of the time-concentration curve. Objective: To exp...

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Main Authors: Asuka Nemoto, MPharm, ME, Matsuura Masaaki, PhD, Kazue Yamaoka, PhD
Format: Article
Language:English
Published: Elsevier 2017-01-01
Series:Current Therapeutic Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0011393X1630131X
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spelling doaj-ceb223d97d8540ea997edf51b9b3b2632020-11-24T21:01:34ZengElsevierCurrent Therapeutic Research0011-393X1879-03132017-01-0184C424910.1016/j.curtheres.2017.04.001A Bayesian Approach for Population Pharmacokinetic Modeling of Alcohol in Japanese IndividualsAsuka Nemoto, MPharm, MEMatsuura Masaaki, PhDKazue Yamaoka, PhDBackground: Blood alcohol concentration data that were previously obtained from 34 healthy Japanese subjects with limited sampling times were reanalyzed. Characteristics of the data were that the concentrations were obtained from only the early part of the time-concentration curve. Objective: To explore significant covariates for the population pharmacokinetic analysis of alcohol by incorporating external data using a Bayesian method, and to estimate effects of the covariates. Methods: The data were analyzed using a Markov chain Monte Carlo Bayesian estimation with NONMEM 7.3 (ICON Clinical Research LLC, North Wales, Pennsylvania). Informative priors were obtained from the external study. Results: A 1-compartment model with Michaelis-Menten elimination was used. The typical value for the apparent volume of distribution was 49.3 L at the age of 29.4 years. Volume of distribution was estimated to be 20.4 L smaller in subjects with the ALDH2*1/*2 genotype than in subjects with the ALDH2*1/*1 genotype. Conclusions: A population pharmacokinetic model for alcohol was updated. A Bayesian approach allowed interpretation of significant covariate relationships, even if the current dataset is not informative about all parameters. This is the first study reporting an estimate of the effect of the ALDH2 genotype in a PPK model.http://www.sciencedirect.com/science/article/pii/S0011393X1630131XPopulation pharmacokineticspharmacogenomicsaldehyde dehydrogenase 2MCMC Bayesian estimationNONMEM
collection DOAJ
language English
format Article
sources DOAJ
author Asuka Nemoto, MPharm, ME
Matsuura Masaaki, PhD
Kazue Yamaoka, PhD
spellingShingle Asuka Nemoto, MPharm, ME
Matsuura Masaaki, PhD
Kazue Yamaoka, PhD
A Bayesian Approach for Population Pharmacokinetic Modeling of Alcohol in Japanese Individuals
Current Therapeutic Research
Population pharmacokinetics
pharmacogenomics
aldehyde dehydrogenase 2
MCMC Bayesian estimation
NONMEM
author_facet Asuka Nemoto, MPharm, ME
Matsuura Masaaki, PhD
Kazue Yamaoka, PhD
author_sort Asuka Nemoto, MPharm, ME
title A Bayesian Approach for Population Pharmacokinetic Modeling of Alcohol in Japanese Individuals
title_short A Bayesian Approach for Population Pharmacokinetic Modeling of Alcohol in Japanese Individuals
title_full A Bayesian Approach for Population Pharmacokinetic Modeling of Alcohol in Japanese Individuals
title_fullStr A Bayesian Approach for Population Pharmacokinetic Modeling of Alcohol in Japanese Individuals
title_full_unstemmed A Bayesian Approach for Population Pharmacokinetic Modeling of Alcohol in Japanese Individuals
title_sort bayesian approach for population pharmacokinetic modeling of alcohol in japanese individuals
publisher Elsevier
series Current Therapeutic Research
issn 0011-393X
1879-0313
publishDate 2017-01-01
description Background: Blood alcohol concentration data that were previously obtained from 34 healthy Japanese subjects with limited sampling times were reanalyzed. Characteristics of the data were that the concentrations were obtained from only the early part of the time-concentration curve. Objective: To explore significant covariates for the population pharmacokinetic analysis of alcohol by incorporating external data using a Bayesian method, and to estimate effects of the covariates. Methods: The data were analyzed using a Markov chain Monte Carlo Bayesian estimation with NONMEM 7.3 (ICON Clinical Research LLC, North Wales, Pennsylvania). Informative priors were obtained from the external study. Results: A 1-compartment model with Michaelis-Menten elimination was used. The typical value for the apparent volume of distribution was 49.3 L at the age of 29.4 years. Volume of distribution was estimated to be 20.4 L smaller in subjects with the ALDH2*1/*2 genotype than in subjects with the ALDH2*1/*1 genotype. Conclusions: A population pharmacokinetic model for alcohol was updated. A Bayesian approach allowed interpretation of significant covariate relationships, even if the current dataset is not informative about all parameters. This is the first study reporting an estimate of the effect of the ALDH2 genotype in a PPK model.
topic Population pharmacokinetics
pharmacogenomics
aldehyde dehydrogenase 2
MCMC Bayesian estimation
NONMEM
url http://www.sciencedirect.com/science/article/pii/S0011393X1630131X
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