dc.contributor.author
Falkenhagen, Undine
dc.contributor.author
Knöchel, Jane
dc.contributor.author
Kloft, Charlotte
dc.contributor.author
Huisinga, Wilhelm
dc.date.accessioned
2023-04-14T11:26:28Z
dc.date.available
2023-04-14T11:26:28Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/38889
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-38605
dc.description.abstract
Quantitative systems pharmacology (QSP) models integrate comprehensive qualitative and quantitative knowledge about pharmacologically relevant processes. We previously proposed a first approach to leverage the knowledge in QSP models to derive simpler, mechanism-based pharmacodynamic (PD) models. Their complexity, however, is typically still too large to be used in the population analysis of clinical data. Here, we extend the approach beyond state reduction to also include the simplification of reaction rates, elimination of reactions, and analytic solutions. We additionally ensure that the reduced model maintains a prespecified approximation quality not only for a reference individual but also for a diverse virtual population. We illustrate the extended approach for the warfarin effect on blood coagulation. Using the model-reduction approach, we derive a novel small-scale warfarin/international normalized ratio model and demonstrate its suitability for biomarker identification. Due to the systematic nature of the approach in comparison with empirical model building, the proposed model-reduction algorithm provides an improved rationale to build PD models also from QSP models in other applications.
en
dc.format.extent
12 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject
quantitative systems pharmacology models
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::615 Pharmakologie, Therapeutik
dc.title
Deriving mechanism-based pharmacodynamic models by reducing quantitative systems pharmacology models: An application to warfarin
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1002/psp4.12903
dcterms.bibliographicCitation.journaltitle
CPT: Pharmacometrics & Systems Pharmacology
dcterms.bibliographicCitation.number
4
dcterms.bibliographicCitation.pagestart
432
dcterms.bibliographicCitation.pageend
443
dcterms.bibliographicCitation.volume
12
dcterms.bibliographicCitation.url
https://doi.org/10.1002/psp4.12903
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Pharmazie
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
2163-8306
refubium.resourceType.provider
WoS-Alert