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Carbohydrate malabsorption is minimal in school-age cystic fibrosis children

R D Hoffman1, J N Isenberg, G K Powell

  • 1Department of Pediatrics, University of Texas Medical Branch, Galveston 77550.

Insights

Children with cystic fibrosis (CF) show minimal carbohydrate malabsorption despite fat and protein issues. Carbohydrate may be a viable energy source for CF patients with high energy needs.

Area of Science:

  • Pediatric Nutrition
  • Gastroenterology
  • Metabolic Disorders

Background:

  • Cystic Fibrosis (CF) leads to significant malabsorption of fats and proteins.
  • Increased energy demands are common in children with CF.
  • Dietary management is crucial for improving nutritional status in CF.

Purpose of the Study:

  • To assess carbohydrate absorption in school-age children with CF.
  • To evaluate the impact of CF on carbohydrate digestion and utilization.
  • To explore alternative energy sources for CF patients.

Main Methods:

  • Balance studies were conducted on 15 school-age children with CF over one year.
  • Stool analysis included conventional methods for fat and protein, and an anthrone method for carbohydrate.
  • Thin-layer chromatography was used to detect short-chain fatty acids in stool.

Main Results:

  • Despite significant fat and protein malabsorption, less than 1% of ingested carbohydrate was lost intact.
  • Fecal carbohydrate excretion was independent of intake, unlike fat and protein.
  • No short-chain fatty acids were detected in stool samples.

Conclusions:

  • Carbohydrate malabsorption is minimal in school-age children with CF.
  • Carbohydrate represents a potentially valuable energy source for CF patients.
  • Further research into carbohydrate utilization in CF is warranted.

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