Predictive value of the complement system for sepsis-induced disseminated intravascular coagulation in septic

Xin Zhao1, Yun-Xia Chen1, Chun-Sheng Li1

  • 1Emergency Department of Beijing Chao-Yang Hospital Affiliated to Capital Medical University, Chaoyang District, Beijing 100020, China.

Journal of Critical Care
|December 31, 2014
PubMed

Insights

Complement component C3, membrane attack complex (MAC), and mannose-binding lectin (MBL) are elevated in sepsis patients with disseminated intravascular coagulation (DIC). MAC independently predicts sepsis-induced DIC and its development post-admission.

Area of Science:

  • Immunology
  • Critical Care Medicine
  • Hematology

Background:

  • Sepsis-induced disseminated intravascular coagulation (DIC) is a life-threatening condition.
  • The role of complement system activation in sepsis-induced DIC requires further elucidation.
  • Understanding complement component changes may offer diagnostic and prognostic insights.

Purpose of the Study:

  • To investigate alterations in circulating complement component C3, membrane attack complex (MAC), and mannose-binding lectin (MBL) in sepsis patients with DIC.
  • To assess the predictive value of these complement components for the development of sepsis-induced DIC.

Main Methods:

  • Adult septic patients were enrolled, with sepsis-induced DIC defined by a DIC score ≥ 5.
  • Circulating levels of C3, MAC, and MBL were measured on emergency department (ED) arrival.
  • Receiver operating characteristic (ROC) curve analysis and logistic regression were used to evaluate predictive values.

Main Results:

  • Complement 3, MAC, and MBL levels were significantly higher in patients with sepsis-induced DIC compared to those without (P < .01).
  • Membrane attack complex (MAC) emerged as an independent predictor of sepsis-induced DIC (AUC = 0.793).
  • MAC and Sequential Organ Failure Assessment score independently predicted the progression to DIC during hospitalization (AUC = 0.741 for MAC).

Conclusions:

  • Circulating levels of C3, MAC, and MBL are elevated in septic patients presenting with DIC.
  • Membrane attack complex (MAC) is a significant independent predictor for both the presence and future development of sepsis-induced DIC.
Abstract

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