Evidence map›Paper›PMID 24877118›Full record

ArticleBioMed research international2014

Exploring population pharmacokinetic modeling with resampling visualization.

Fenghua Zuo, Jun Li, Xiaoyong Sun

Abstract read
In one paragraph

Article in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Fenghua ZuoCollege of Information Engineering, Taishan Medical University, Taian, Shandong 271016, China.
Jun LiFaculté de Pharmacie, Université de Montréal, CP 6128, Succursale Centre-Ville, Montréal , QC, Canada H3C 3J7 ; Centre de Recherche Mathématiques, Université de Montréal, CP 6128, Succursale Centre-Ville, Montréal , QC, Canada H3C 3J7.ORCID 0000-0002-1112-7555
Xiaoyong SunAgricultural Big Data Research Center, College of Information Science and Engineering, Shandong Agricultural University, Taian, Shandong 271018, China.ORCID 0000-0002-2425-3526

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn the last decade, population pharmacokinetic (PopPK) modeling has spread its influence in the whole process of drug research and development. While targeting the construction of the dose-concentration of a drug based on a population of patients, it shows great flexibility in dealing with sparse samplings and unbalanced designs. The resampling approach has been considered an important statistical tool to assist in PopPK model validation by measuring the uncertainty of parameter estimates and evaluating the influence of individuals.

methodsThe current work describes a graphical diagnostic approach for PopPK models by visualizing resampling statistics, such as case deletion and bootstrap. To examine resampling statistics, we adapted visual methods from multivariate analysis, parallel coordinate plots, and multidimensional scaling.

resultsMultiple models were fitted, the information of parameter estimates and diagnostics were extracted, and the results were visualized. With careful scaling, the dependencies between different statistics are revealed. Using typical examples, the approach proved to have great capacity to identify influential outliers from the statistical perspective, which deserves special attention in a dosing regimen. DISCUSSION: By combining static graphics with interactive graphics, we are able to explore the multidimensional data from an integrated and systematic perspective. Complementary to current approaches, our proposed method provides a new way for PopPK modeling analysis.

Indexed as

Models, TheoreticalPharmacokineticsUser-Computer InterfaceDrug Discovery

Identifiers

PMID24877118
PMCPMC4024412

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.