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Children on continuous ambulatorial peritoneal dialysis: muscle and plasma proteins, amino acids and nutritional

A Canepa1, J C Divino Filho, A M Forsberg

  • 1Department of Nephrology, Istituto Giannina Gaslini, Genova, Italy.

Clinical Nephrology
|August 1, 1996
PubMed

Insights

Children on continuous ambulatory peritoneal dialysis (CAPD) show altered plasma amino acid levels, with essential amino acids reduced and non-essential ones elevated. Muscle amino acid levels were largely similar to controls, indicating complex nutritional changes in pediatric CAPD patients.

Area of Science:

  • Pediatric Nephrology
  • Nutritional Biochemistry
  • Clinical Chemistry

Background:

  • Continuous ambulatory peritoneal dialysis (CAPD) is a treatment for pediatric end-stage renal disease.
  • Nutritional status is a critical concern in children undergoing CAPD.
  • Amino acid (AA) profiles may reflect nutritional derangements in CAPD patients.

Purpose of the Study:

  • To investigate plasma and muscle amino acid levels in children on CAPD.
  • To explore the relationship between amino acid levels and nutritional status indicators in this population.

Main Methods:

  • Evaluated 10 children on CAPD (mean age 6.4 years) and 22 surgical controls.
  • Collected muscle biopsies (rectus abdominis) and fasting venous blood samples.
  • Measured plasma and muscle intracellular free amino acid concentrations.
  • Assessed nutritional status using alkali-soluble protein (ASP)/DNA ratio, serum albumin, transferrin, and body mass index (BMI).

Main Results:

  • Plasma essential AA (valine, leucine, isoleucine, lysine, methionine, tyrosine) were significantly reduced in CAPD children compared to controls.
  • Plasma non-essential AA (aspartic acid, glycine, citrulline, 1-3 methihystidine, taurine + alanine) were significantly elevated.
  • Muscle intracellular free essential AA levels, except valine and leucine, did not differ significantly.
  • Muscle non-essential AA (aspartic acid, glutamic acid, ornithine) showed increased intracellular concentrations.
  • No significant correlations between AA levels and ASP/DNA ratio, albumin, transferrin, or bicarbonate.
  • Muscle ASP/DNA ratio correlated significantly with age (r = 0.714, p < 0.05).
  • Muscle Branched Chain Amino Acid (BCAA) levels correlated significantly with BMI (r = 0.648, p < 0.05).

Conclusions:

  • Pediatric CAPD patients exhibit distinct alterations in plasma amino acid profiles, characterized by reduced essential and elevated non-essential AA.
  • Muscle amino acid composition is relatively preserved, suggesting compartmental differences in AA handling.
  • Age and BMI show significant correlations with muscle protein indicators and BCAA levels, respectively, highlighting their importance in nutritional assessment for pediatric CAPD.
  • Further research is needed to elucidate the mechanisms behind these AA derangements and their clinical implications.

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