Quantifying energy expenditure in childhood: utility in managing pediatric metabolic disorders

Laura P E Watson1, Katherine S Carr1, Michelle C Venables2,3

  • 1National Institute for Health Research (NIHR) Cambridge Clinical Research Facility, Addenbrooke's Hospital, Cambridge, United Kingdom.

Insights

New equations predict resting energy expenditure (REE) in children with thyroid disorders by comparing them to healthy peers. This method helps identify metabolic abnormalities and monitor treatment effectiveness.

Area of Science:

  • Pediatric Endocrinology
  • Metabolic Disorders
  • Biostatistics

Background:

  • Standard energy expenditure prediction equations may not accurately reflect metabolic abnormalities in disease cohorts.
  • Tailoring equations to specific patient populations, like those with thyroid disorders, is crucial for accurate assessment.

Purpose of the Study:

  • To develop and validate prediction equations for resting energy expenditure (REE) in pediatric patients with thyroid disorders.
  • To utilize a healthy pediatric cohort for equation development and comparison.

Main Methods:

  • Derived a prediction equation for REE using indirect calorimetry and DXA-measured body composition in 101 healthy children.
  • Validated the equation in a separate group of 100 healthy children.
  • Applied the derived equation and z-score analysis to pediatric patients with resistance to thyroid hormone (RTH) disorders (β and α types).

Main Results:

  • The derived REE prediction equation was: REE = 0.061 * Lean soft tissue (kg) - 0.138 * Sex + 2.41 (R² = 0.816).
  • Pediatric patients with RTHβ showed mean REE z scores of -0.02 ± 1.26.
  • RTHα patients exhibited z scores of -1.69 (male) and -2.05 (female).

Conclusions:

  • A novel methodology allows for the expression of REE differences in pediatric metabolic disorders as z scores compared to healthy peers.
  • This z-score approach facilitates the monitoring of REE changes following clinical interventions, such as thyroxine treatment in RTHα patients.
Abstract

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