Membrane biocompatibility does not affect whole body protein metabolism during dialysis

JM Veeneman, HA Kingma, F Stellaard, PE de Jong, DJ Reijngoud, RM Huisman*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

2 Citations (Scopus)

Abstract

Background: Protein-calorie malnutrition is present in 30-50% of dialysis patients. The lack of biocompatibility of the dialysis membrane, which results in low-grade inflammation, could be responsible for this malnutrition. We investigated whether protein-energy malnutrition could be partly due to incompatibility of the dialyzer during the dialysis session. Methods: Five patients were dialyzed during 2 periods of 3 weeks (cross-over) with either a single-use low-flux polysulfone or cellulose triacetate (biocompatible) or a single-use cuprophan (bio-incompatible) membrane. As a measure of whole body protein metabolism, a primed constant infusion of L-[1-C-13]-valine was used during a 4-hour dialysis session. Results: Cuprophan was a more powerful activator of the complement system than other membranes. Protein metabolism parameters during both study protocols were not different and resulted in the same protein balance during polysulfone/cellulose triacetate (-15 +/- 3) and cuprophan (-13 +/- 2 mu mol/kg/h) dialysis. Conclusion: In stable hemodialysis patients with no apparent complications, protein metabolism during dialysis is not affected by the compatibility of the dialysis membrane. Copyright (C) 2005 S. Karger AG, Basel.

Original languageEnglish
Pages (from-to)211-218
Number of pages8
JournalBlood purification
Volume23
Issue number3
DOIs
Publication statusPublished - 2005

Keywords

  • amino acid
  • hemodialysis
  • protein turnover
  • stable isotope
  • valine
  • CHRONIC-HEMODIALYSIS PATIENTS
  • CHRONIC-RENAL-FAILURE
  • AMINO-ACID LOSSES
  • NUTRITIONAL PARAMETERS
  • CATABOLISM
  • PLASMA
  • CONSEQUENCES
  • ALBUMIN
  • LEUCINE
  • PATIENT

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