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.
Abstract

Related Concept Videos

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 a challenge in...
Blood Studies for Cardiovascular System I: Cardiac Biomarkers01:20

Blood Studies for Cardiovascular System I: Cardiac Biomarkers

Cardiac biomarkers are enzymes, proteins, and hormones released into the blood when cardiac cells are injured. They are powerful tools for triaging.
The essential diagnostic tools for detecting myocardial necrosis and monitoring individuals suspected of having acute coronary syndrome (ACS) include:
Troponins
Troponins, particularly cardiac troponins I and T, are the most precise and sensitive markers of myocardial injury. They are detectable within 4-6 hours of myocardial injury and remain...
Acute Kidney Injury IV: Diagnostic Studies and Prevention01:30

Acute Kidney Injury IV: Diagnostic Studies and Prevention

Accurate diagnosis and effective prevention are critical in managing Acute Kidney Injury (AKI), which is linked to high mortality rates ranging from 10% to 80%. Timely recognition of at-risk patients and careful monitoring can significantly reduce the likelihood of kidney damage.Diagnostic Assessments:The diagnostic process starts with a comprehensive medical history to identify prerenal, intrarenal, and postrenal causes.Prerenal causes, such as dehydration, hypotension, or blood loss, should...
Overview of Protein Metabolism01:21

Overview of Protein Metabolism

Proteins are broken down into amino acids during digestion. Unlike fats and carbohydrates, which are stored for later use, proteins are not. Instead, amino acids are either used to produce ATP through oxidation or contribute to the creation of new proteins for the growth and repair of the body. Any surplus amino acids from the diet are converted into glucose or triglycerides rather than excreted.
Amino acids play various roles in the body once they are absorbed into cells. They are restructured...
Measurement of Bioavailability: Pharmacokinetic Methods01:30

Measurement of Bioavailability: Pharmacokinetic Methods

Pharmacokinetics is a vital branch of pharmacology that examines how drugs are absorbed, distributed, metabolized, and excreted by the body. Two key methodologies in pharmacokinetics are plasma drug concentration studies and urinary drug excretion analyses, both of which provide critical insights into a drug's therapeutic efficacy and bioavailability.Plasma Drug Concentration-Time StudiesPlasma drug concentration-time studies involve analyzing blood samples at specific intervals to quantify...
Measurement of Bioavailability: Pharmacodynamic Methods01:20

Measurement of Bioavailability: Pharmacodynamic Methods

Pharmacodynamic methods provide insights into a drug's effects on physiological processes over time and play a crucial role in understanding bioavailability and therapeutic efficacy. These methods can be broadly classified into acute pharmacological and therapeutic response approaches, each with distinct mechanisms and applications.The acute pharmacological response method directly correlates a drug's physiological effects, such as ECG or pupil diameter changes, to its time course in the body.