Dietary acid load in children with chronic kidney disease

Michelle López1, Greysi Moreno2, Gustavo Lugo3

  • 1Department of Nephrology, Children's Hospital José Manuel de los Ríos. Departament of Pediatrics, Centro Médico Docente La Trinidad, Caracas, Venezuela. michellelopez27@gmail.com.

Insights

Children with chronic kidney disease (CKD) in Venezuela exhibit dietary patterns contributing to metabolic acidosis, a risk factor for disease progression. Assessing potential renal acid load (PRAL) is crucial for nutritional guidance in pediatric CKD patients.

Area of Science:

  • Pediatric Nephrology
  • Nutritional Science
  • Metabolic Health

Background:

  • Western diets are linked to high acid loads, potentially causing metabolic acidosis.
  • Metabolic acidosis is a known contributor to the progression of chronic kidney disease (CKD).
  • Understanding dietary acid load is crucial for managing pediatric CKD.

Purpose of the Study:

  • To estimate the potential renal acid load (PRAL) in children with CKD.
  • To evaluate the acid-base status in these patients.
  • To identify dietary factors contributing to metabolic acidosis in pediatric CKD.

Main Methods:

  • Studied 27 children with CKD in Caracas, Venezuela.
  • Assessed diet using food frequency questionnaires and 24-h intake reminders.
  • Calculated PRAL using the Remer and Manz method; analyzed serum creatinine, electrolytes, and venous gases.

Main Results:

  • Protein intake exceeded recommendations in 78.6% of patients; vegetable and fruit intake was low.
  • Mean PRAL was 16 ± 10.7 mEq/day, correlating positively with energy, protein, and fat intake.
  • 80.7% of patients had metabolic acidosis, with serum pH 7.3 ± 0.08 and bicarbonate 20.46 ± 4.5 mEq/L.

Conclusions:

  • The dietary patterns of Venezuelan children with CKD may promote metabolic acidosis, risking disease progression.
  • Unfavorable dietary acid loads are implicated in the progression of pediatric CKD.
  • PRAL assessment is recommended for nutritional counseling in children with CKD.
Abstract

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