Robust Optimal Design for the Estimation of Hyperparameters in Population Pharmacokinetics

The expectation of the determinant of the inverse of the population Fisher information matrix is proposed as a criterion to evaluate and optimize designs for the estimation of population pharmacokinetic (PK) parameters. Given a PK model, a measurement error model, a parametric distribution of the pa...

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Published in:Journal of pharmacokinetics and biopharmaceutics Vol. 26; no. 6; pp. 689 - 716
Main Authors: Tod, Michel, Mentré, France, Merlé, Yann, Mallet, Alain
Format: Journal Article
Language:English
Published: New York, NY Plenum 01.12.1998
Springer Nature B.V
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ISSN:0090-466X, 1567-567X, 1573-8744
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Abstract The expectation of the determinant of the inverse of the population Fisher information matrix is proposed as a criterion to evaluate and optimize designs for the estimation of population pharmacokinetic (PK) parameters. Given a PK model, a measurement error model, a parametric distribution of the parameters and a prior distribution representing the belief about the hyperparameters to be estimated, the EID criterion is minimized in order to find the optimal population design. In this approach, a group is defined as a number of subjects to whom the same sampling schedule (i.e., the number of samples and their timing) is applied. The constraints, which are defined a priori, are the number of groups, the size of each group and the number of samples per subject in each group. The goal of the optimization is to determine the optimal sampling times in each group. This criterion is applied to a one-compartment open model with first-order absorption. The error model is either homoscedastic or heteroscedastic with constant coefficient of variation. Individual parameters are assumed to arise from a lognormal distribution with mean vector M and covariance matrix C. Uncertainties about the M and C are accounted for by a prior distribution which is normal for M and Wishart for C. Sampling times are optimized by using a stochastic gradient algorithm. Influence of the number of different sampling schemes, the number of subjects per sampling schedule, the number of samples per subject in each sampling scheme, the uncertainties on M and C and the assumption about the error model and the dose have been investigated.
AbstractList The expectation of the determinant of the inverse of the population Fisher information matrix is proposed as a criterion to evaluate and optimize designs for the estimation of population pharmacokinetic (PK) parameters. Given a PK model, a measurement error model, a parametric distribution of the parameters and a prior distribution representing the belief about the hyperparameters to be estimated, the EID criterion is minimized in order to find the optimal population design. In this approach, a group is defined as a number of subjects to whom the same sampling schedule (i.e., the number of samples and their timing) is applied. The constraints, which are defined a priori, are the number of groups, the size of each group and the number of samples per subject in each group. The goal of the optimization is to determine the optimal sampling times in each group. This criterion is applied to a one-compartment open model with first-order absorption. The error model is either homoscedastic or heteroscedastic with constant coefficient of variation. Individual parameters are assumed to arise from a lognormal distribution with mean vector M and covariance matrix C. Uncertainties about the M and C are accounted for by a prior distribution which is normal for M and Wishart for C. Sampling times are optimized by using a stochastic gradient algorithm. Influence of the number of different sampling schemes, the number of subjects per sampling schedule, the number of samples per subject in each sampling scheme, the uncertainties on M and C and the assumption about the error model and the dose have been investigated. [PUBLICATION ABSTRACT]
The expectation of the determinant of the inverse of the population Fisher information matrix is proposed as a criterion to evaluate and optimize designs for the estimation of population pharmacokinetic (PK) parameters. Given a PK model, a measurement error model, a parametric distribution of the parameters and a prior distribution representing the belief about the hyperparameters to be estimated, the EID criterion is minimized in order to find the optimal population design. In this approach, a group is defined as a number of subjects to whom the same sampling schedule (i.e., the number of samples and their timing) is applied. The constraints, which are defined a priori, are the number of groups, the size of each group and the number of samples per subject in each group. The goal of the optimization is to determine the optimal sampling times in each group. This criterion is applied to a one-compartment open model with first-order absorption. The error model is either homoscedastic or heteroscedastic with constant coefficient of variation. Individual parameters are assumed to arise from a lognormal distribution with mean vector M and covariance matrix C. Uncertainties about the M and C are accounted for by a prior distribution which is normal for M and Wishart for C. Sampling times are optimized by using a stochastic gradient algorithm. Influence of the number of different sampling schemes, the number of subjects per sampling schedule, the number of samples per subject in each sampling scheme, the uncertainties on M and C and the assumption about the error model and the dose have been investigated.
The expectation of the determinant of the inverse of the population Fisher information matrix is proposed as a criterion to evaluate and optimize designs for the estimation of population pharmacokinetic (PK) parameters. Given a PK model, a measurement error model, a parametric distribution of the parameters and a prior distribution representing the belief about the hyperparameters to be estimated, the EID criterion is minimized in order to find the optimal population design. In this approach, a group is defined as a number of subjects to whom the same sampling schedule (i.e., the number of samples and their timing) is applied. The constraints, which are defined a priori, are the number of groups, the size of each group and the number of samples per subject in each group. The goal of the optimization is to determine the optimal sampling times in each group. This criterion is applied to a one-compartment open model with first-order absorption. The error model is either homoscedastic or heteroscedastic with constant coefficient of variation. Individual parameters are assumed to arise from a lognormal distribution with mean vector M and covariance matrix C. Uncertainties about the M and C are accounted for by a prior distribution which is normal for M and Wishart for C. Sampling times are optimized by using a stochastic gradient algorithm. Influence of the number of different sampling schemes, the number of subjects per sampling schedule, the number of samples per subject in each sampling scheme, the uncertainties on M and C and the assumption about the error model and the dose have been investigated.The expectation of the determinant of the inverse of the population Fisher information matrix is proposed as a criterion to evaluate and optimize designs for the estimation of population pharmacokinetic (PK) parameters. Given a PK model, a measurement error model, a parametric distribution of the parameters and a prior distribution representing the belief about the hyperparameters to be estimated, the EID criterion is minimized in order to find the optimal population design. In this approach, a group is defined as a number of subjects to whom the same sampling schedule (i.e., the number of samples and their timing) is applied. The constraints, which are defined a priori, are the number of groups, the size of each group and the number of samples per subject in each group. The goal of the optimization is to determine the optimal sampling times in each group. This criterion is applied to a one-compartment open model with first-order absorption. The error model is either homoscedastic or heteroscedastic with constant coefficient of variation. Individual parameters are assumed to arise from a lognormal distribution with mean vector M and covariance matrix C. Uncertainties about the M and C are accounted for by a prior distribution which is normal for M and Wishart for C. Sampling times are optimized by using a stochastic gradient algorithm. Influence of the number of different sampling schemes, the number of subjects per sampling schedule, the number of samples per subject in each sampling scheme, the uncertainties on M and C and the assumption about the error model and the dose have been investigated.
Author Tod, Michel
Mentré, France
Merlé, Yann
Mallet, Alain
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Cites_doi 10.1109/TAC.1974.1100716
10.1093/biomet/84.2.429
10.1016/0025-5564(85)90068-9
10.1080/01621459.1966.10502018
10.1023/A:1016267811074
10.1016/0169-2607(96)01721-X
10.1007/BF01070904
10.1214/aoms/1177706705
10.4153/CJM-1960-030-4
10.1007/BF01062273
10.1007/BF01062528
10.1016/0025-5564(90)90141-K
10.1023/A:1025701327672
10.1177/009286159502900321
10.1007/s002280050199
10.1007/BF03036255
10.1007/BF03190258
10.2165/00003088-199222060-00004
10.1016/0025-5564(88)90097-1
10.2165/00003088-199630020-00001
10.1146/annurev.pa.32.040192.001153
10.1007/BF02353491
10.1016/0010-4809(72)90051-1
10.1016/0005-1098(90)90116-Y
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ISSN 0090-466X
1567-567X
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Issue 6
Keywords Human
Optimal sampling
Compartmental model
Methodology
Simulation
Experimental design
Estimation
Population
Kinetic parameter
Pharmacokinetics
Optimization
Sampling frequency
Language English
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PublicationTitle Journal of pharmacokinetics and biopharmaceutics
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Springer Nature B.V
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References E. I. Ette (409593_CR9) 1995; 12
E. Walter (409593_CR16) 1987; 253
J. Kiefer (409593_CR27) 1960; 12
L. B. Sheiner (409593_CR2) 1992; 32
M. Tod (409593_CR21) 1996; 50
A. H. Thomson (409593_CR5) 1992; 22
V. Breant (409593_CR11) 1996; 51
E. N. Jonsson (409593_CR10) 1996; 24
P. Burtin (409593_CR4) 1996; 22
S. Vozeh (409593_CR3) 1996; 30
N. L. Johnson (409593_CR19) 1972
E. Walter (409593_CR14) 1990; 26
H. Kesten (409593_CR22) 1958; 29
409593_CR28
M. Tod (409593_CR25) 1997; 25
L. Pronzato (409593_CR17) 1985; 75
G. N. Saridis (409593_CR20) 1974; 19
409593_CR23
L. Pronzato (409593_CR26) 1988; 89
D. Z. D'Argenio (409593_CR15) 1981; 9
P. L. Odell (409593_CR24) 1966; 313
J. Wang (409593_CR8) 1992; 20
D. Z. D'Argenio (409593_CR18) 1990; 99
F. Mentré (409593_CR13) 1997; 84
Y. Hashimoto (409593_CR7) 1991; 19
L. B. Sheiner (409593_CR1) 1972; 5
F. Mentré (409593_CR12) 1995; 29
M. K. Al-Banna (409593_CR6) 1990; 18
References_xml – volume: 19
  start-page: 798
  year: 1974
  ident: 409593_CR20
  publication-title: IEEE Trans. Automat. Contr.
  doi: 10.1109/TAC.1974.1100716
– volume: 84
  start-page: 429
  year: 1997
  ident: 409593_CR13
  publication-title: Biometrika
  doi: 10.1093/biomet/84.2.429
– volume: 75
  start-page: 103
  year: 1985
  ident: 409593_CR17
  publication-title: Math. Biosci.
  doi: 10.1016/0025-5564(85)90068-9
– volume: 313
  start-page: 199
  year: 1966
  ident: 409593_CR24
  publication-title: J. Am. Statist. Soc.
  doi: 10.1080/01621459.1966.10502018
– volume: 12
  start-page: 729
  year: 1995
  ident: 409593_CR9
  publication-title: Pharm. Res.
  doi: 10.1023/A:1016267811074
– volume: 50
  start-page: 13
  year: 1996
  ident: 409593_CR21
  publication-title: Comput. Meth. Prog. Biomed.
  doi: 10.1016/0169-2607(96)01721-X
– volume: 9
  start-page: 739
  year: 1981
  ident: 409593_CR15
  publication-title: J. Pharmacokin. Biopharm.
  doi: 10.1007/BF01070904
– volume: 29
  start-page: 41
  year: 1958
  ident: 409593_CR22
  publication-title: Ann. Math. Statist.
  doi: 10.1214/aoms/1177706705
– volume: 12
  start-page: 362
  year: 1960
  ident: 409593_CR27
  publication-title: Can. J. Math.
  doi: 10.4153/CJM-1960-030-4
– volume: 253
  start-page: R530
  year: 1987
  ident: 409593_CR16
  publication-title: Am. J. Physiol.
– ident: 409593_CR23
– volume: 18
  start-page: 347
  year: 1990
  ident: 409593_CR6
  publication-title: J. Pharmacokin. Biopharm.
  doi: 10.1007/BF01062273
– volume: 20
  start-page: 279
  year: 1992
  ident: 409593_CR8
  publication-title: J. Pharmacokin. Biopharm.
  doi: 10.1007/BF01062528
– volume: 99
  start-page: 105
  year: 1990
  ident: 409593_CR18
  publication-title: Math. Biosci.
  doi: 10.1016/0025-5564(90)90141-K
– volume: 25
  start-page: 515
  year: 1997
  ident: 409593_CR25
  publication-title: J. Pharmacokin. Biopharm.
  doi: 10.1023/A:1025701327672
– volume: 29
  start-page: 997
  year: 1995
  ident: 409593_CR12
  publication-title: Drug Inform. J.
  doi: 10.1177/009286159502900321
– volume: 51
  start-page: 283
  year: 1996
  ident: 409593_CR11
  publication-title: Eur. J. Clin. Pharmacol.
  doi: 10.1007/s002280050199
– volume: 19
  start-page: 333
  year: 1991
  ident: 409593_CR7
  publication-title: J. Pharmacokin. Biopharm.
  doi: 10.1007/BF03036255
– start-page: 158
  volume-title: Distributions in Statistics: Continuous Multivariate Distributions
  year: 1972
  ident: 409593_CR19
– ident: 409593_CR28
– volume: 22
  start-page: 105
  year: 1996
  ident: 409593_CR4
  publication-title: Eur. J. Drug Metab. Pharmacokin
  doi: 10.1007/BF03190258
– volume: 22
  start-page: 447
  year: 1992
  ident: 409593_CR5
  publication-title: Clin. Pharmacokin.
  doi: 10.2165/00003088-199222060-00004
– volume: 89
  start-page: 161
  year: 1988
  ident: 409593_CR26
  publication-title: Math. Biosci.
  doi: 10.1016/0025-5564(88)90097-1
– volume: 30
  start-page: 81
  year: 1996
  ident: 409593_CR3
  publication-title: Clin. Pharmacokin.
  doi: 10.2165/00003088-199630020-00001
– volume: 32
  start-page: 185
  year: 1992
  ident: 409593_CR2
  publication-title: Ann. Rev. Pharmacol. Toxicol.
  doi: 10.1146/annurev.pa.32.040192.001153
– volume: 24
  start-page: 245
  year: 1996
  ident: 409593_CR10
  publication-title: J. Pharmacokin. Biopharm.
  doi: 10.1007/BF02353491
– volume: 5
  start-page: 441
  year: 1972
  ident: 409593_CR1
  publication-title: Comput. Biomed. Res.
  doi: 10.1016/0010-4809(72)90051-1
– volume: 26
  start-page: 195
  year: 1990
  ident: 409593_CR14
  publication-title: Automatica
  doi: 10.1016/0005-1098(90)90116-Y
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Snippet The expectation of the determinant of the inverse of the population Fisher information matrix is proposed as a criterion to evaluate and optimize designs for...
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SubjectTerms Biological and medical sciences
General pharmacology
Humans
Medical sciences
Models, Biological
Pharmacokinetics
Pharmacokinetics. Pharmacogenetics. Drug-receptor interactions
Pharmacology. Drug treatments
Population Surveillance
Studies
Title Robust Optimal Design for the Estimation of Hyperparameters in Population Pharmacokinetics
URI https://www.ncbi.nlm.nih.gov/pubmed/10485081
https://www.proquest.com/docview/916240105
https://www.proquest.com/docview/69255338
Volume 26
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