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.

Related Concept Videos

Pharmacokinetics in Pediatric Patients: Drug Distribution01:17

Pharmacokinetics in Pediatric Patients: Drug Distribution

Drug distribution in the pediatric population exhibits unique challenges and considerations due to the physiological differences between children, particularly neonates and infants, and adults. A crucial aspect of pediatric pharmacology is understanding how these differences impact the pharmacokinetics of various drugs, necessitating age-specific dosing strategies to ensure efficacy and safety.Neonates and infants have a higher total body water content, ~75%–90% of their body weight,...
150
Drug Dosing: Obese Patients01:21

Drug Dosing: Obese Patients

In the United States, obesity is a prominent concern. It is linked to heightened mortality rates due to increased occurrences of conditions such as hypertension, atherosclerosis, coronary artery disease, and diabetes compared to nonobese individuals. A patient is classified as obese if their actual body weight surpasses the ideal or desirable body weight by 20%, based on Metropolitan Life Insurance Company data. Ideal body weights consider average weights and heights for males and females...
106
Dosage Regimens: Partial Pharmacokinetic Parameters01:01

Dosage Regimens: Partial Pharmacokinetic Parameters

It is not uncommon for complete drug pharmacokinetic profiles to remain elusive in pharmacokinetics. This necessitates certain educated assumptions by pharmacokineticists to determine appropriate dosage regimens without comprehensive pharmacokinetic data from animal or human studies. One prevalent assumption is setting the bioavailability factor, denoted as F, to 1 or 100%. This assumption caters to the scenario where a drug doesn't achieve full systemic absorption, resulting in the patient...
71
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
100
Drug Dosing: Infants and Children01:29

Drug Dosing: Infants and Children

Pediatric patient dosages diverge from adults due to disparities in body surface area, total body water, and extracellular fluid per kilogram of body weight. The dosing regimen considers the variations in pharmacokinetics and pharmacology across distinct age groups, encompassing preterm newborns, infants, young children, older children, and adolescents. Calculation of pediatric patient doses is predicated on determining body surface area, which exhibits a superior correlation with the child's...
125
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption01:23

Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption

Understanding the physiological differences in the pediatric population is crucial for effective pharmacotherapy. Neonates, infants, and children exhibit significant variations in gastric pH, gastric emptying time, intestinal transit time, and biliary function. These variations profoundly affect oral drug absorption, necessitating a nuanced approach to pediatric dosing.Neonates present with a unique physiological profile, having a gastric pH greater than 4 and faster and more irregular gastric...
131