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Whole body protein kinetics measured with a non-invasive method in severely burned children
Elisabet Børsheim1, David L Chinkes, Serina J McEntire
1Shriners Hospitals for Children/Galveston, Department of Surgery, University of Texas Medical Branch, Galveston, TX 77550, USA. elborshe@utmb.edu
Insights
Severe burns elevate protein turnover in children even after healing. This study used a safe, non-invasive method to measure whole body protein metabolism in burned children at discharge, revealing significant differences compared to healthy controls.
Area of Science:
- Biochemistry
- Pediatric Medicine
- Metabolic Research
Background:
- Severe burns cause persistent skeletal muscle catabolism.
- Whole body protein metabolism in burned children during long-term recovery is not well understood.
Purpose of the Study:
- To measure whole body protein turnover in children recently discharged after severe burns.
- To compare protein metabolism in burned children with healthy controls using a non-invasive method.
Main Methods:
- Utilized a stable isotope method with a single oral dose of (15)N-alanine.
- Collected urine for 34 hours to calculate whole body protein flux, synthesis, and breakdown.
- Compared measurements between nine burned children and twelve healthy children.
Main Results:
- Burned children at discharge exhibited significantly elevated total protein turnover (4.53±0.65 g/kg/day) compared to controls (3.20±0.22 g/kg/day).
- Protein synthesis was also higher in burned children.
- A trend towards increased protein breakdown was observed in burned children.
Conclusions:
- Total protein turnover remains elevated in children at discharge following severe burns, suggesting a prolonged stress response.
- The oral (15)N-alanine bolus method is confirmed as a practical, safe, and non-invasive technique for assessing total body protein turnover.
Unlabelled:
Persistent and extensive skeletal muscle catabolism is characteristic of severe burns. Whole body protein metabolism, an important component of this process, has not been measured in burned children during the long-term convalescent period. The aim of this study was to measure whole body protein turnover in burned children at discharge (95% healed) and in healthy controls by a non-invasive stable isotope method. Nine burned children (7 boys, 2 girls; 54±14 (S.D.)% total body area burned; 13±4 years; 45±20 kg; 154±14 cm) and 12 healthy children (8 boys, 4 girls; 12±3 years; 54±16 kg; 150±22 cm) were studied. A single oral dose of (15)N-alanine (16 mg/kg) was given, and thereafter urine was collected for 34 h. Whole body protein flux was calculated from labeling of urinary urea nitrogen. Then, protein synthesis was calculated as protein flux minus excretion, and protein breakdown as flux minus intake. At discharge, total protein turnover was 4.53±0.65 (S.E.)g kg body weight(-1) day(-1) in the burned children compared to 3.20±0.22 g kg(-1) day(-1) in controls (P=0.02). Expressed relative to lean body mass (LBM), the rates were 6.12±0.94 vs. 4.60±0.36 g kg LBM(-1) day(-1) in burn vs. healthy (P=0.06). Total protein synthesis was also elevated in burned vs. healthy children, and a tendency for elevated protein breakdown was observed.
Conclusion:
Total protein turnover is elevated in burned children at discharge compared to age-matched controls, possibly reflecting the continued stress response to severe burn. The oral (15)N-alanine bolus method is a convenient, non-invasive, and no-risk method for measurement of total body protein turnover.
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