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Published on: January 28, 2020
Endocan is a stable circulating molecule in ICU patients
Alexandre Gaudet1, Camille Chenevier-Gobeaux2, Erika Parmentier1
1Univ. Lille, U1019 - UMR 8204 - CIIL - Center for Infection and Immunity of Lille, F-59000 Lille, France; CNRS, UMR 8204, F-59000 Lille, France; INSERM, U1019, F-59000 Lille, France; CHU Lille, Pôle de Réanimation, Hôpital Roger Salengro, F-59000 Lille, France; Institut Pasteur de Lille, F-59000 Lille, France.
Endocan, a biomarker for pneumonia and acute respiratory distress syndrome (ARDS), demonstrates stability in various blood samples, including EDTA plasma, ensuring reliable measurements in intensive care unit (ICU) patients.
Area of Science:
- Biochemistry
- Clinical Chemistry
- Proteomics
Background:
- Endocan is a lung endothelial cell-secreted proteoglycan with significant physiological roles.
- It serves as a potential biomarker for pneumonia and acute respiratory distress syndrome (ARDS).
- Proinflammatory cytokines like TNF-α induce endocan secretion, but proteolytic degradation can cause preanalytical variations.
Purpose of the Study:
- To investigate the stability of endocan in different blood collection and storage conditions.
- To assess potential interferences affecting endocan measurement accuracy.
- To validate endocan as a reliable biomarker in clinical settings.
Main Methods:
- Evaluated endocan stability in serum, plasma, and whole blood using various anticoagulants and protease inhibitors.
- Performed recovery tests to assess dilution effects.
- Assessed stability under different storage conditions (room temperature, freeze-thaw cycles) and interference from sample quality (hemolysis, icterus, turbidity).
Main Results:
- EDTA tubes showed minimal interference in blood collection.
- No significant dilution effect was observed in recovery tests.
- Patient plasma endocan remained stable at room temperature for up to 72 hours and after three freeze-thaw cycles.
- Hemolytic, icteric, or turbid samples did not interfere with endocan measurement.
Conclusions:
- Endocan measurements in intensive care unit (ICU) patients are accurate and reliable.
- The stability of endocan in collected samples supports its utility as a biomarker.
- Low endocan levels observed in ICU patients who develop ARDS are likely to be trustworthy.
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