Reduced ADAMTS13 in children with severe meningococcal sepsis is associated with severity and outcome

Tamara N Bongers1, Marieke Emonts, Moniek P M de Maat

  • 1Erasmus Medical Centre, Department of Hematology, Rotterdam, The Netherlands.

Insights

In pediatric meningococcal sepsis, low ADAMTS13 activity and high von Willebrand factor (VWF) levels are linked to disease severity and poor outcomes. These imbalances in coagulation factors may drive harmful microthrombi formation.

Area of Science:

  • Pediatric critical care medicine
  • Hematology
  • Infectious diseases

Background:

  • Pediatric meningococcal sepsis frequently causes multiple organ failure.
  • Coagulation and fibrinolysis imbalances, including elevated ultra-large von Willebrand factor (VWF), contribute to sepsis severity.
  • ADAMTS13 regulates VWF activity, influencing its role in plasma.

Purpose of the Study:

  • To investigate the association between ADAMTS13, VWF, and the severity and outcome of pediatric meningococcal sepsis.
  • To analyze the dynamic changes in these markers during intensive care unit (ICU) stay.

Main Methods:

  • Measured ADAMTS13 activity and antigen, VWF collagen binding activity (VWF:CB), VWF antigen (VWF:Ag), VWF propeptide, and factor VIII in 58 children with severe meningococcal sepsis.
  • Assessed these markers at multiple time points during ICU admission.

Main Results:

  • In the acute phase, ADAMTS13 activity and antigen were decreased, while VWF:CB and VWF:Ag levels were significantly increased.
  • Lower ADAMTS13 antigen and VWF:CB levels were observed in non-survivors compared to survivors.
  • ADAMTS13 activity and VWF:CB correlated with disease severity, as indicated by the Pediatric Risk of Mortality score.

Conclusions:

  • Decreased ADAMTS13 activity and elevated VWF levels characterize the acute phase of severe meningococcal sepsis in children.
  • These hemostatic alterations are related to disease severity and patient outcomes.
  • The findings suggest a role for ADAMTS13 and VWF dysregulation in the pathogenesis of thrombotic complications in sepsis.

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