Individualizing the use of medications in children: making Goldilocks happy.
Document Type
Article
Publication Date
9-2014
Identifier
DOI: 10.1038/clpt.2014.130
Abstract
To date, implementation of precision medicine for children has been limited. Extrapolation of adult experience streamlines pediatric drug development programs, and physiologically based pharmacokinetic models aid pediatric dose selection on a population basis. To achieve clinically viable individualization of drug therapy, genotype-stratified pharmacokinetic studies can efficiently characterize the extremes of the dose-exposure relationship. Reducing variability in exposure through genotype-based dosing may improve identification of genetic factors contributing to response, ultimately improving drug therapy for children.
Journal Title
Clinical pharmacology and therapeutics
Volume
96
Issue
3
First Page
304
Last Page
306
MeSH Keywords
Age Factors; Child; Child, Preschool; Dose-Response Relationship, Drug; Drug Dosage Calculations; Genotype; Humans; Infant; Infant, Newborn; Patient Safety; Pharmaceutical Preparations; Pharmacogenetics; Pharmacokinetics; Phenotype; Risk Assessment; Risk Factors
Keywords
Age Factors; Dose-Response Relationship, Drug; Drug Dosage Calculations; Genotype; Patient Safety; Pharmaceutical Preparations; Pharmacogenetics; Pharmacokinetics; Phenotype; Risk Assessment; Risk Factors
Recommended Citation
Leeder, J. S., Brown, J. T., Soden, S. E. Individualizing the use of medications in children: making Goldilocks happy. Clinical pharmacology and therapeutics 96, 304-306 (2014).
Comments
Grant support