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Dietary supplement and nutrition in children with cystic fibrosis

Insights

Nutritional status in cystic fibrosis of the pancreas (CFP) impacts growth. A specialized dietary supplement improved weight, clinical scores, and reduced white blood cell (WBC) counts in CFP patients.

Area of Science:

  • Pediatric Nutrition
  • Gastroenterology
  • Biochemistry

Background:

  • Poor growth is common in cystic fibrosis of the pancreas (CFP).
  • Nutritional status markers like albumin, urea nitrogen, cholesterol, and white blood cell (WBC) counts correlate with growth in CFP patients.
  • CFP patients exhibit growth deceleration after age 8.

Purpose of the Study:

  • To assess the impact of a specialized dietary supplement on the nutritional status and growth of patients with CFP.
  • To evaluate changes in clinical scores and serological markers following nutritional intervention.

Main Methods:

  • A cohort of 15 CFP patients received a year-long dietary supplement (beef serum hydrolysate, glucose polymer, medium-chain triglycerides).
  • Nutritional status was assessed through weight, clinical scores, serum albumin, and WBC counts.
  • Outcomes were compared to a control group of CFP patients not receiving the supplement.

Main Results:

  • Patients receiving the dietary supplement showed significant weight gain.
  • A significant increase in clinical scores and serum albumin levels was observed.
  • The intervention led to a significant reduction in WBC counts compared to controls.

Conclusions:

  • The specialized dietary supplement effectively improved nutritional status in CFP patients.
  • Nutritional intervention can positively impact growth, clinical outcomes, and inflammatory markers in CFP.
  • Dietary supplementation is a viable strategy to manage poor growth and associated complications in cystic fibrosis of the pancreas.

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