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Published on: October 14, 2025
Corticosteroids increase protein breakdown and loss in newly diagnosed pediatric Crohn disease
Steven J Steiner1, Joshua D Noe, Scott C Denne
1Department of Pediatrics, James Whitcomb Riley Hospital for Children, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA. ssteiner@iupui.edu
Insights
Corticosteroid therapy in children with Crohn disease significantly increased protein breakdown and loss. This finding highlights potential negative impacts on body composition during treatment for pediatric Crohn disease.
Area of Science:
- Pediatric Gastroenterology
- Metabolic Research
- Biochemistry
Background:
- Children with Crohn disease often experience impaired growth and altered body composition.
- Previous research indicated reduced protein breakdown with corticosteroid or anti-TNF-α therapy.
Purpose of the Study:
- To investigate whole-body protein metabolism in children with newly diagnosed Crohn disease undergoing corticosteroid therapy.
Main Methods:
- Utilized stable isotopes ([d5] phenylalanine, [1-(13)C] leucine, [(15)N(2)] urea) to assess protein kinetics in a fasting state.
- Metabolic assessments were conducted on children with suspected Crohn disease and controls, with follow-up assessments after 2 weeks of corticosteroid treatment for Crohn disease patients.
Main Results:
- No significant differences in protein breakdown or loss were observed between newly diagnosed Crohn disease patients and controls at baseline.
- Following 2 weeks of corticosteroid therapy, Crohn disease patients showed significant increases in phenylalanine (32%) and leucine (26%) appearance rates, indicating elevated protein breakdown.
- A substantial increase in urea appearance rate (273%) was noted, signifying increased protein loss.
Conclusions:
- Corticosteroid therapy in children with newly diagnosed Crohn disease leads to a significant increase in whole-body protein breakdown and loss.
- These metabolic changes induced by corticosteroids may significantly impact body composition in pediatric Crohn disease patients.
Abstract:
Children with Crohn disease have altered growth and body composition. Previous studies have demonstrated decreased protein breakdown after either corticosteroid or anti-TNF-α therapy. The aim of this study was to evaluate whole body protein metabolism during corticosteroid therapy in children with newly diagnosed Crohn disease. Children with suspected Crohn disease and children with abdominal symptoms not consistent with Crohn disease underwent outpatient metabolic assessment. Patients diagnosed with Crohn disease and prescribed corticosteroid therapy returned in 2 wk for repeat metabolic assessment. Using the stable isotopes [d5] phenylalanine, [1-(13)C] leucine, and [(15)N(2)] urea, protein kinetics were determined in the fasting state. Thirty-one children (18 controls and 13 newly diagnosed with Crohn disease) completed the study. There were no significant differences in protein breakdown or loss between patients with Crohn disease at diagnosis and controls. After corticosteroid therapy in patients with Crohn disease, the rates of appearance of phenylalanine (32%) and leucine (26%) increased significantly, reflecting increased protein breakdown, and the rate of appearance of urea also increased significantly (273%), reflecting increased protein loss. Whole body protein breakdown and loss increased significantly after 2 wk of corticosteroid therapy in children with newly diagnosed Crohn disease, which may have profound effects on body composition.
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