Endothelial adhesion molecules and multiple organ failure in patients with severe sepsis

Bravein Amalakuhan, Sheila A. Habib, Mandeep Mangat, Luis F. Reyes, Alejandro H. Rodriguez, Cecilia A. Hinojosa, Nilam J. Soni, Ryan P. Gilley, Carlos A. Bustamante, Antonio Anzueto, Stephanie M. Levine, Jay I. Peters, Stefano Aliberti, Oriol Sibila, James D. Chalmers, Antoni Torres, Grant W. Waterer, Ignacio Martin-Loeches, Jose Bordon, Jose BlanquerFrancisco Sanz, Pedro J. Marcos, Jordi Rello, Julio Ramirez, Jordi Solé-Violán, Carlos M. Luna, Charles Feldman, Martin Witzenrath, Richard G. Wunderink, Daiana Stolz, Tim L. Wiemken, Yuichiro Shindo, Charles S. Dela Cruz, Carlos J. Orihuela, Marcos I. Restrepo (Lead / Corresponding author)

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    56 Citations (Scopus)
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    Abstract

    Objective To determine if serum levels of endothelial adhesion molecules were associated with the development of multiple organ failure (MOF) and in-hospital mortality in adult patients with severe sepsis. 

    Design This study was a secondary data analysis of a prospective cohort study. 

    Setting Patients were admitted to two tertiary intensive care units in San Antonio, TX, between 2007 and 2012. 

    Patients Patients with severe sepsis at the time of intensive care unit (ICU) admission were enrolled. Inclusion criteria were consistent with previously published criteria for severe sepsis or septic shock in adults. Exclusion criteria included immunosuppressive medications or conditions.

    Interventions None. 

    Measurements Baseline serum levels of the following endothelial cell adhesion molecules were measured within the first 72 h of ICU admission: Intracellular Adhesion Molecule 1 (ICAM-1), Vascular Cell Adhesion Molecule-1 (VCAM-1), and Vascular Endothelial Growth Factor (VEGF). The primary and secondary outcomes were development of MOF (⩾2 organ dysfunction) and in-hospital mortality, respectively. Main results Forty-eight patients were enrolled in this study, of which 29 (60%) developed MOF. Patients that developed MOF had higher levels of VCAM-1 (p = 0.01) and ICAM-1 (p = 0.01), but not VEGF (p = 0.70) compared with patients without MOF (single organ failure only). The area under the curve (AUC) to predict MOF according to VCAM-1, ICAM-1 and VEGF was 0.71, 0.73, and 0.54, respectively. Only increased VCAM-1 levels were associated with in-hospital mortality (p = 0.03). These associations were maintained even after adjusting for APACHE and SOFA scores using logistic regression. 

    Conclusions High levels of serum ICAM-1 was associated with the development of MOF. High levels of VCAM-1 was associated with both MOF and in-hospital mortality.

    Original languageEnglish
    Pages (from-to)267-273
    Number of pages7
    JournalCytokine
    Volume88
    Early online date1 Oct 2016
    DOIs
    Publication statusPublished - Dec 2016

    Keywords

    • Biomarkers
    • Intracellular Adhesion Molecule-1
    • Mortality
    • Multiple organ failure
    • Sepsis
    • Shock
    • Vascular Cell Adhesion Molecule-1
    • Vascular Endothelial Growth Factor

    ASJC Scopus subject areas

    • Immunology and Allergy
    • Immunology
    • Biochemistry
    • Hematology
    • Molecular Biology

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