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Published on: June 7, 2024
Body Composition Using Air Displacement Plethysmography in Children With Inflammatory Bowel Disease
Jasbir Dhaliwal1, Inez Martincevic2, Brock Williams2
1Division of Gastroenterology, Hepatology and Nutrition.
Insights
Excess body fatness affects nearly 25% of pediatric inflammatory bowel disease (IBD) patients and may be missed by standard obesity screenings. Early Infliximab drug exposure was not affected by this excess adiposity.
Area of Science:
- Pediatric gastroenterology
- Clinical nutrition
- Pharmacokinetics
Background:
- Inflammatory bowel disease (IBD) affects children and adolescents.
- Body composition and adiposity are crucial factors in pediatric IBD management.
- Assessing body fatness accurately in this population is essential for optimal care.
Purpose of the Study:
- To evaluate body composition in pediatric IBD patients.
- To determine the accuracy of common clinical tools in identifying excess body fatness.
- To explore the impact of adiposity on Infliximab pharmacokinetics during early treatment.
Main Methods:
- Prospective cohort study of 5-17 year olds with IBD starting Infliximab.
- Body composition assessed via air displacement plethysmography (ADP).
- Excess adiposity defined by fat mass index (FMI ≥75th centile); compared with BMI and arm fat area (AFA).
Main Results:
- 24% of pediatric IBD patients exhibited excess adiposity (FMI ≥75th centile).
- Standard metrics like BMI and AFA alone missed cases of excess adiposity.
- No significant difference in Infliximab trough levels was observed based on adiposity levels.
Conclusions:
- Excess adiposity is prevalent in pediatric IBD and often undetected by routine screening.
- Current anthropometric methods may not adequately identify excess body fat in these children.
- Early Infliximab exposure appears unaffected by excess adiposity in pediatric IBD patients.
Objective:
The aim of the study was to assess the body composition of children with inflammatory bowel disease (IBD) and to study the accuracy of clinically available tools in predicting excess body fatness. We aimed at also exploring the influence of adiposity on pharmacokinetics during early Infliximab exposure.
Methods:
Prospective cohort study in 5- to 17-year-old children with IBD initiating Infliximab therapy. Patient demographic, phenotypic, and laboratory data at the time of Infliximab initiation were recorded. Body composition was assessed using air displacement plethysmography (ADP). fat mass index (FMI = fat mass [kg]/(height [m])) was calculated to determine excess adiposity (defined as FMI ≥75th centile). Anthropometrics (weight, height, mid upper arm circumference [MUAC] and triceps skin fold thickness [TSF]) were obtained and MUAC and TSF measurements were used to calculate arm fat area (AFA) and arm muscle area z-scores. Statistical analysis was applied as appropriate.
Results:
Fifty-three (68% male; 55% Crohn disease [CD], 45% ulcerative colitis [UC], median [IQR] age 15 [13-16] years) children with IBD were included. Twenty-four percentage of children with IBD (21% CD, 29% UC) had excess adiposity. Four children (31%) with FMI ≥75th centile were not identified by body mass index (BMI) alone (kappa of 0.60), and 2 children (15%) were not identified by AFA z-score alone. The intra- and interobserver reliability of MUAC and TSFT measurements was excellent. There was no difference in Infliximab trough levels at the end of induction between those with FMI less than or ≥75th centile.
Conclusions:
Excess adiposity affects approximately 1 in 4 young patients with IBD and can be missed by routine obesity screening. Our exploratory study did not raise concerns of underexposure to infliximab in those children with excess adiposity during early drug exposure.
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