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Published on: April 1, 2014
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.
Abstract:
Multiple organ failure is a common feature of pediatric meningococcal sepsis and is associated with an imbalance of coagulation and fibrinolysis. This is partly due to an increased secretion of prothrombotic ultra-large von Willebrand factor (VWF) as the result of vascular endothelial damage. Another factor that may contribute is ADAMTS13, which converts VWF into smaller, less active, VWF multimers and thus influences VWF activity in plasma. We investigated the role of ADAMTS13 and VWF in the severity and outcome of sepsis. In 58 children with severe meningococcal sepsis we measured ADAMTS13 activity and antigen, VWF collagen binding activity (VWF:CB) and antigen levels (VWF:Ag), VWF propeptide and factor VIII at different time points during their stay in the paediatric intensive care unit. In the acute phase, both ADAMTS13 activity and antigen were decreased (median 23.4% and 33.7% of normal, respectively) and VWF:CB and VWF:Ag levels were strongly increased (325% and 348%, respectively.) ADAMTS13 antigen (23.9% vs. 34.6%; p=0.06) and VWF:CB (240% and 340% p<0.001) were lower in non-survivors than in survivors. ADAMTS13 activity and VWF:CB were both correlated with the severity of the disease, as indicated by the Pediatric Risk of Mortality score (R(s)= -0.38 and R(s)= -0.50, p=0.01, respectively, p<0.001). In the acute phase of severe sepsis decreased levels of ADAMTS13 and increased levels of VWF are observed, and the changes are related to severity of disease and outcome. This may contribute to the formation of microthrombi and the severity of thrombotic sequelae of sepsis.
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