The metabolic response to ingested protein is normal in long-term hemodialysis patients

  • JM Veeneman
  • , HA Kingma
  • , TS Boer
  • , F Stellaard
  • , PE de Jong
  • , DJ Reijngoud
  • , RM Huisman*
  • *Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    7 Citations (Scopus)

    Abstract

    Background Protein-energy malnutrition affects 30% to 50% of hemodialysis (HD) patients. This has been attributed to inadequate food intake, but may be caused by disturbances in utilization of ingested protein. Methods: We studied protein kinetics during fasting and during ingestion of a protein-enriched meal to investigate possible metabolic differences between stable HD patients and control subjects. Whole-body protein kinetics was measured by means of a primed constant infusion of L[1-C-13] valine. Results: During fasting, whole-body protein balance was significantly less negative in HD patients compared with control subjects. During meal intake, protein balance was similar between HD patients and control subjects. Meal intake increased protein balance significantly in both groups, but not differently between the groups. Also, protein oxidation was decreased during fasting in HD patients compared with control subjects, but not during meal intake. Conclusion: We conclude that the rate of protein breakdown is lower in HD patients compared with control subjects, but the efficiency of protein utilization is normal in HD patients during a nondialysis day.

    Original languageEnglish
    Pages (from-to)330-341
    Number of pages12
    JournalAmerican Journal of Kidney Diseases
    Volume43
    Issue number2
    DOIs
    Publication statusPublished - Feb-2004
    Event33rd Annual Meeting of the American-Society-of-Nephrology - , Canada
    Duration: 10-Oct-200016-Oct-2000

    Keywords

    • valine turnover
    • protein synthesis
    • stable isotopes
    • amino acids
    • protein intake
    • hemodialysis (HD)
    • WHOLE-BODY PROTEIN
    • CHAIN AMINO-ACIDS
    • CHRONIC-RENAL-FAILURE
    • NITROGEN HOMEOSTASIS
    • LEUCINE METABOLISM
    • MASS-SPECTROMETRY
    • TURNOVER
    • DIALYSIS
    • KINETICS
    • BALANCE

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