Sepsis biomarkers

Clin Chim Acta. 2015 Feb 2:440:97-103. doi: 10.1016/j.cca.2014.11.012. Epub 2014 Nov 18.

Abstract

Sepsis is the most frequent cause of death in non-coronary intensive care units (ICUs). In the past 10 years, progress has been made in the early identification of septic patients and in their treatment and these improvements in support and therapy mean that the mortality is gradually decreasing but it still remains unacceptably high. Leaving clinical diagnosis aside, the laboratory diagnostics represent a complex range of investigations that can place significant demands on the system given the speed of response required. There are hundreds of biomarkers which could be potentially used for diagnosis and prognosis in septic patients. The main attributes of successful markers would be high sensitivity, specificity, possibility of bed-side monitoring, and financial accessibility. Only a fraction is used in routine clinical practice because many lack sufficient sensitivity or specificity. The following review gives a short overview of the current epidemiology of sepsis, its pathogenesis and state-of-the-art knowledge on the use of specific biochemical, hematological and immunological parameters in its diagnostics. Prospective approaches towards discovery of new diagnostic biomarkers have been shortly mentioned.

Keywords: Biomarkers; SIRS; Sensitivity; Sepsis; Specificity.

Publication types

  • Review

MeSH terms

  • Acute-Phase Proteins
  • Biomarkers / analysis*
  • Biomarkers / blood
  • C-Reactive Protein / analysis
  • Calcitonin / blood
  • Carrier Proteins / blood
  • Cytokines / blood
  • Fibrin Fibrinogen Degradation Products / analysis
  • Humans
  • Intensive Care Units
  • Leukocytes / metabolism
  • Lipopolysaccharide Receptors / blood
  • Membrane Glycoproteins / blood
  • Peptide Fragments / blood
  • Protein Precursors / blood
  • Sepsis / diagnosis*
  • Sepsis / metabolism*
  • Systemic Inflammatory Response Syndrome / diagnosis
  • Systemic Inflammatory Response Syndrome / metabolism

Substances

  • Acute-Phase Proteins
  • Biomarkers
  • Carrier Proteins
  • Cytokines
  • Fibrin Fibrinogen Degradation Products
  • Lipopolysaccharide Receptors
  • Membrane Glycoproteins
  • Peptide Fragments
  • Protein Precursors
  • fibrin fragment D
  • lipopolysaccharide-binding protein
  • presepsin protein, human
  • Calcitonin
  • C-Reactive Protein