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Originally published In Press as doi:10.1194/jlr.M200401-JLR200 on January 16, 2003
Journal of Lipid Research, Vol. 44, 754-761, April 2003
Copyright © 2003 by Lipid Research, Inc.
Plasma ceramide and lysophosphatidylcholine inversely correlate with mortality in sepsis patients
Wolfgang Drobnik*,
Gerhard Liebisch*,
Franz-Xaver Audebert ,
Dieter Fröhlich ,
Thomas Glück ,
Peter Vogel**,
Gregor Rothe* and
Gerd Schmitz1,*
* Institute for Clinical Chemistry, University of Regensburg, Germany
Laboratory Medicine, Department of Anesthesiology, University of Regensburg, Germany
Department of Internal Medicine I, University of Regensburg, Germany
** Department of Surgery, University of Regensburg, Germany
1 To whom correspondence should be addressed. e-mail: gerd.schmitz{at}klinik.uni-regensburg.de
Recent data indicate that ceramide (Cer) and lysophosphatidylcholine (LPC) regulate immune cell functions. Since these bioactive lipids are generated in blood plasma by inflammatory lipases, we hypothesized that they may be involved in the process of acute systemic sepsis. In order to provide support for this hypothesis, we analyzed the plasma levels of Cer and LPC by quantitative tandem mass spectrometry in 102 sepsis patients starting with the day at which the sepsis criteria were fulfilled for the first time, as well as on day 4 and day 11. The values were compared with 56 healthy controls and correlated with sepsis-related mortality within 30 days of study entry. Most Cer species were increased in sepsis patients, while all LPC species were markedly decreased. In addition, we determined the molar ratios with their precursor molecules sphingomyelin (SPM) and phosphatidylcholine (PC), which reflect the enzymatic reactions responsible for their formation. Species-specific as well as total Cer-SPM ratios were increased, whereas LPC-PC ratios were decreased in sepsis patients. The increased Cer-SPM ratios as well as the decreased LPC-PC ratios showed a strong predictive power for sepsis-related mortality.
Together with existing data from in vitro experiments and animal models, the results provide the first ex vivo indication for the role of Cer and lysophospholipids in systemic inflammation in humans.
Abbreviations: AUC, area under the curve; Cer, ceramide; LPC, lysophosphatidylcholine; PC, phosphatidylcholine; ROC, receiver operating curve; SPM, sphingomyelin Supplementary key words outcome lipoproteins sphingomyelinase phospholipase SAPS score prognostic marker

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Copyright © 2003 by the American Society for Biochemistry and Molecular Biology.
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