CD64-Neutrophil expression and stress metabolic patterns in early sepsis and severe traumatic brain injury in

Diana-Michaela Fitrolaki1, Helen Dimitriou, Maria Kalmanti

  • 1Pediatric Intensive Care Unit, University Hospital of Heraklion, 71110 Heraklion, Crete, Greece.

BMC Pediatrics
|March 5, 2013
PubMed

Insights

Children with sepsis exhibit distinct metabolic changes, including high neutrophils expressing CD64, glucose, and triglycerides, alongside low cholesterol and lipoproteins, differing from traumatic brain injury patients. These patterns persist for three days.

Area of Science:

  • Pediatric Critical Care Medicine
  • Metabolic Disorders in Critical Illness
  • Immunology and Flow Cytometry

Background:

  • Critical illness causes significant metabolic derangements in children.
  • Sepsis and severe traumatic brain injury (TBI) present distinct metabolic profiles.
  • Understanding these patterns aids in diagnosing and managing critically ill children.

Purpose of the Study:

  • To compare acute phase metabolic patterns in children with sepsis (S), severe sepsis/septic shock (SS), TBI, and healthy controls (C).
  • To evaluate the relationship between metabolic patterns and neutrophil, lymphocyte, and monocyte expression of CD64 and CD11b.
  • To identify early metabolic markers differentiating sepsis from TBI in critically ill children.

Main Methods:

  • Sixty children were studied, including 45 with systemic inflammatory response syndrome (SIRS) divided into TBI, S, and SS groups (n=15 each), and 15 healthy controls (C).
  • Flow cytometry assessed CD64 and CD11b expression on immune cells.
  • Procalcitonin (PCT), C-reactive protein (CRP), glucose, triglycerides (TG), total cholesterol (TC), HDL, and LDL were measured, with repeat measures in SIRS groups.

Main Results:

  • Sepsis groups (S and SS) showed significantly higher CRP, PCT, and TG compared to TBI and C.
  • Septic groups had significantly lower TC, LDL, and HDL than C and TBI.
  • Increased neutrophil CD64 (nCD64) expression strongly correlated with higher CRP, PCT, glucose, and TG, and lower cholesterol and lipoproteins in sepsis.

Conclusions:

  • Sepsis is characterized by a high CD64, glucose, and TG, low cholesterol/lipoprotein metabolic pattern, distinct from TBI.
  • These metabolic patterns and associated CD64 expression persist for the first three days of acute illness.
  • CD64 expression on neutrophils serves as a marker for the acute phase metabolic derangement in sepsis.
Abstract

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