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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2015
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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 |
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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 |
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