Cargando…

A population pharmacokinetic model for R- and S-citalopram and desmethylcitalopram in Alzheimer’s disease patients with agitation

The citalopram for Alzheimer’s disease trial evaluated citalopram for the management for agitation in Alzheimer’s disease patients. Sparse data was available from this elderly patient population. A nonlinear mixed effects population pharmacokinetic modeling approach was used to describe the pharmaco...

Descripción completa

Detalles Bibliográficos
Autores principales: Akil, Ayman, Bies, Robert R., Pollock, Bruce G., Avramopoulos, Dimitrios, Devanand, D. P., Mintzer, Jacobo E., Porsteinsson, Anton P., Schneider, Lon S., Weintraub, Daniel, Yesavage, Jerome, Shade, David M., Lyketsos, Constantine G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4720707/
https://www.ncbi.nlm.nih.gov/pubmed/26611790
http://dx.doi.org/10.1007/s10928-015-9457-6
_version_ 1782411108727914496
author Akil, Ayman
Bies, Robert R.
Pollock, Bruce G.
Avramopoulos, Dimitrios
Devanand, D. P.
Mintzer, Jacobo E.
Porsteinsson, Anton P.
Schneider, Lon S.
Weintraub, Daniel
Yesavage, Jerome
Shade, David M.
Lyketsos, Constantine G.
author_facet Akil, Ayman
Bies, Robert R.
Pollock, Bruce G.
Avramopoulos, Dimitrios
Devanand, D. P.
Mintzer, Jacobo E.
Porsteinsson, Anton P.
Schneider, Lon S.
Weintraub, Daniel
Yesavage, Jerome
Shade, David M.
Lyketsos, Constantine G.
author_sort Akil, Ayman
collection PubMed
description The citalopram for Alzheimer’s disease trial evaluated citalopram for the management for agitation in Alzheimer’s disease patients. Sparse data was available from this elderly patient population. A nonlinear mixed effects population pharmacokinetic modeling approach was used to describe the pharmacokinetics of R- and S-citalopram and their primary metabolite (desmethylcitalopram). A structural model with 4 compartments (one compartment/compound) with linear oral absorption and elimination described the data adequately. Overall, the model showed that clearance of the R-enantiomer was slower than the clearance of the S-enantiomer. Without accounting for any patient-specific covariates, the population estimate of the metabolic clearance of citalopram was 8.6 (R-citalopram) and 14 L/h (S-citalopram). The population estimate of the clearance of desmethylcitalopram was 23.8 (R-Dcit) and 38.5 L/h (S-Dcit). Several patient-specific covariates were found to have a significant effect on the pharmacokinetics of R,S-citalopram and desmethylcitalopram. A significant difference in the metabolic clearance of R-citalopram between males and females (13 vs 9.05 L/h) was identified in this analysis. Both R- and S-citalopram metabolic clearance decreased with age. Additionally, consistent with literature reports S-citalopram metabolic clearance increased with increasing body weight and was significantly influenced by CYPC19 genotype, with a difference of 5.8 L/h between extensive/rapid and intermediate/poor metabolizers. R,S-desmethylcitalopram clearance increased with increasing body weight. This model may allow for the opportunity to delineate the effect of R- and S-citalopram on pharmacodynamics outcomes related to the management of agitation in Alzheimer’s disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10928-015-9457-6) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4720707
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-47207072016-01-28 A population pharmacokinetic model for R- and S-citalopram and desmethylcitalopram in Alzheimer’s disease patients with agitation Akil, Ayman Bies, Robert R. Pollock, Bruce G. Avramopoulos, Dimitrios Devanand, D. P. Mintzer, Jacobo E. Porsteinsson, Anton P. Schneider, Lon S. Weintraub, Daniel Yesavage, Jerome Shade, David M. Lyketsos, Constantine G. J Pharmacokinet Pharmacodyn Original Paper The citalopram for Alzheimer’s disease trial evaluated citalopram for the management for agitation in Alzheimer’s disease patients. Sparse data was available from this elderly patient population. A nonlinear mixed effects population pharmacokinetic modeling approach was used to describe the pharmacokinetics of R- and S-citalopram and their primary metabolite (desmethylcitalopram). A structural model with 4 compartments (one compartment/compound) with linear oral absorption and elimination described the data adequately. Overall, the model showed that clearance of the R-enantiomer was slower than the clearance of the S-enantiomer. Without accounting for any patient-specific covariates, the population estimate of the metabolic clearance of citalopram was 8.6 (R-citalopram) and 14 L/h (S-citalopram). The population estimate of the clearance of desmethylcitalopram was 23.8 (R-Dcit) and 38.5 L/h (S-Dcit). Several patient-specific covariates were found to have a significant effect on the pharmacokinetics of R,S-citalopram and desmethylcitalopram. A significant difference in the metabolic clearance of R-citalopram between males and females (13 vs 9.05 L/h) was identified in this analysis. Both R- and S-citalopram metabolic clearance decreased with age. Additionally, consistent with literature reports S-citalopram metabolic clearance increased with increasing body weight and was significantly influenced by CYPC19 genotype, with a difference of 5.8 L/h between extensive/rapid and intermediate/poor metabolizers. R,S-desmethylcitalopram clearance increased with increasing body weight. This model may allow for the opportunity to delineate the effect of R- and S-citalopram on pharmacodynamics outcomes related to the management of agitation in Alzheimer’s disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10928-015-9457-6) contains supplementary material, which is available to authorized users. Springer US 2015-11-26 2016 /pmc/articles/PMC4720707/ /pubmed/26611790 http://dx.doi.org/10.1007/s10928-015-9457-6 Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Paper
Akil, Ayman
Bies, Robert R.
Pollock, Bruce G.
Avramopoulos, Dimitrios
Devanand, D. P.
Mintzer, Jacobo E.
Porsteinsson, Anton P.
Schneider, Lon S.
Weintraub, Daniel
Yesavage, Jerome
Shade, David M.
Lyketsos, Constantine G.
A population pharmacokinetic model for R- and S-citalopram and desmethylcitalopram in Alzheimer’s disease patients with agitation
title A population pharmacokinetic model for R- and S-citalopram and desmethylcitalopram in Alzheimer’s disease patients with agitation
title_full A population pharmacokinetic model for R- and S-citalopram and desmethylcitalopram in Alzheimer’s disease patients with agitation
title_fullStr A population pharmacokinetic model for R- and S-citalopram and desmethylcitalopram in Alzheimer’s disease patients with agitation
title_full_unstemmed A population pharmacokinetic model for R- and S-citalopram and desmethylcitalopram in Alzheimer’s disease patients with agitation
title_short A population pharmacokinetic model for R- and S-citalopram and desmethylcitalopram in Alzheimer’s disease patients with agitation
title_sort population pharmacokinetic model for r- and s-citalopram and desmethylcitalopram in alzheimer’s disease patients with agitation
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4720707/
https://www.ncbi.nlm.nih.gov/pubmed/26611790
http://dx.doi.org/10.1007/s10928-015-9457-6
work_keys_str_mv AT akilayman apopulationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT biesrobertr apopulationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT pollockbruceg apopulationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT avramopoulosdimitrios apopulationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT devananddp apopulationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT mintzerjacoboe apopulationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT porsteinssonantonp apopulationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT schneiderlons apopulationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT weintraubdaniel apopulationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT yesavagejerome apopulationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT shadedavidm apopulationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT lyketsosconstantineg apopulationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT akilayman populationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT biesrobertr populationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT pollockbruceg populationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT avramopoulosdimitrios populationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT devananddp populationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT mintzerjacoboe populationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT porsteinssonantonp populationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT schneiderlons populationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT weintraubdaniel populationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT yesavagejerome populationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT shadedavidm populationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation
AT lyketsosconstantineg populationpharmacokineticmodelforrandscitalopramanddesmethylcitalopraminalzheimersdiseasepatientswithagitation