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Assessment of Child Anthropometry in a Large Epidemiologic Study
Published on: February 2, 2017
Estimation of Body Fat Percentage for Clinical Pharmacokinetic Studies in Children
Thomas P Green1, Helen J Binns1,2,3, Huali Wu4
1Department of Pediatrics, Ann & Robert H. Lurie Children's Hospital of Chicago and Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Insights
Childhood obesity impacts drug pharmacokinetics (PK). This study found body fat percentage (BF%) estimation methods are accurate for evaluating BF% as a PK covariate in pediatric clinical trials.
Area of Science:
- Pediatric pharmacology
- Obesity research
- Clinical trial methodology
Background:
- Childhood obesity is common and affects drug pharmacokinetics (PK).
- Accurate assessment of body fat percentage (BF%) is crucial for understanding drug behavior in children.
- Existing methods for estimating BF% vary in accuracy and precision.
Purpose of the Study:
- To evaluate the covariate effect of body fat percentage (BF%) on pediatric drug pharmacokinetics (PK).
- To compare the accuracy and precision of different BF% estimation methods.
- To assess the utility of these methods in clinical trials.
Main Methods:
- Analysis of two large databases for BF% values in healthy and obese children.
- Comparison of clinical and demographic BF% estimation techniques against dual-x-ray absorptiometry.
- Simulation studies to evaluate method utility in PK clinical trials.
Main Results:
- Bio-impedance and demographic techniques showed high accuracy (<1%) and precision (SD ≤5%) compared to dual-x-ray absorptiometry.
- BF% estimation methods were valuable when their precision exceeded unexplained PK variability.
- Sex and obesity stage explained 68% of BF% variance with BMI.
Conclusions:
- Accurate BF% estimation methods are available for pediatric PK studies.
- BF% can be reliably estimated using sex and obesity stage for PK clinical trials.
- This facilitates the evaluation of BF% as a significant PK covariate in children.
Abstract:
Obesity is a prevalent childhood condition and the degree of adiposity appears likely to be an important covariate in the pharmacokinetics (PKs) of many drugs. We undertook these studies to facilitate the evaluation and, where appropriate, quantification of the covariate effect of body fat percentage (BF%) on PK parameters in children. We examined two large databases to determine the values and variabilities of BF% in children with healthy body weights and in those with obesity, comparing the accuracy and precision of BF% estimation by both clinical methods and demographically derived techniques. Additionally, we conducted simulation studies to evaluate the utility of the several methods for application in clinical trials. BF% was correlated with body mass index (BMI), but was highly variable among both children with healthy body weights and those with obesity. Bio-impedance and several demographically derived techniques produced mean estimates of BF% that differed from dual x-ray absorptiometry by < 1% (accuracy) and a SD of 5% or less (precision). Simulation studies confirmed that when the differences in precision among the several methods were small compared with unexplained between-subject variability of a PK parameter, the techniques were of similar value in assessing the contribution of BF%, if any, as a covariate for that PK parameter. The combination of sex and obesity stage explained 68% of the variance of BF% with BMI. The estimation of BF% from sex and obesity stage can routinely be applied to PK clinical trials to evaluate the contribution of BF% as a potential covariate.
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