Differential effects of lipoprotein apheresis by lipidfiltration or dextran sulfate adsorption on lipidomic profile

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • J. Gräßler - , Department of Internal Medicine III, University Hospital Carl Gustav Carus Dresden (Author)
  • S. Kopprasch - , University Hospital Carl Gustav Carus Dresden (Author)
  • J. Passauer - , University Hospital Carl Gustav Carus Dresden (Author)
  • S. Fischer - , Department of Internal Medicine III, University Hospital Carl Gustav Carus Dresden (Author)
  • K. Schuhmann - , University Hospital Carl Gustav Carus Dresden, Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • S. Bergmann - , University Hospital Carl Gustav Carus Dresden (Author)
  • G. Siegert - , Institute for Clinical Chemistry and Laboratory Medicine (Author)
  • A. Shevchenko - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • S. R. Bornstein - , Department of Internal Medicine III, University Hospital Carl Gustav Carus Dresden (Author)
  • U. Julius - , University Hospital Carl Gustav Carus Dresden (Author)

Abstract

Objective and methods: Acute modification of plasma lipidomic profile was assessed by top-down shotgun profiling on a LTQ Orbitrap hybrid mass spectrometer in 14 patients treated with two different apheresis techniques: plasma lipidfiltration (LF) and whole blood dextran sulfate adsorption (DSA). Results: Patients treated with DSA revealed a significantly more pronounced reduction of LDL-cholesterol (LDL-C), a diminished decrease of HDL-cholesterol (HDL-C) and triglycerides (TG), and a similar reduction in lipoprotein (a) (Lp(a)) level. Against the overall tendency of reduction of lipid metabolites of all lipid classes in post-apheresis plasma, independent of apheresis technology applied, a highly significant increase of phosphatidylethanolamines (PE) in response to DSA was observed. Conclusion: These data indicate that DSA technology may be associated with an activation or damage of blood cells at contact surface which subsequently leads to a massive liberation of cellular and membrane PE's. Pathophysiological consequences, especially with respect to coagulation system and oxidative stress, have to be further elucidated.

Details

Original languageEnglish
Pages (from-to)151-155
Number of pages5
JournalAtherosclerosis Supplements
Volume14
Issue number1
Publication statusPublished - Jan 2013
Peer-reviewedYes

External IDs

PubMed 23357157

Keywords

Keywords

  • Coagulation, Lipidomics, Membrane lipids, Oxidative stress, Phosphatidylethanolamines, Whole blood and plasma lipoprotein apheresis