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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.
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.
Purpose:
To investigate changes in circulating complement component C3, membrane attack complex (MAC), and mannose-binding lectin (MBL) in patients with sepsis-induced disseminated intravascular coagulation (DIC).
Materials And Methods:
Adult septic patients admitted to the emergency department (ED) of Beijing Chao-Yang Hospital were enrolled. A DIC score of 5 or higher was considered sepsis-induced DIC. Circulating C3, MAC, and MBL levels were detected on ED arrival and compared between patients with and without DIC. The predictive value of C3, MAC, and MBL for sepsis-induced DIC at ED arrival and development of DIC after admission were assessed by receiver operating characteristic curve and logistic regression.
Results:
We enrolled 267 septic patients between February and December 2013. Complement 3, MAC, and MBL were higher in the DIC group (P < .01). Membrane attack complex was the independent predictor of sepsis-induced DIC. The area under the curve of MAC in predicting sepsis-induced DIC was 0.793. During hospitalization, 25 patients without DIC at enrollment developed DIC. Membrane attack complex and Sequential Organ Failure Assessment independently predicted progress to DIC. The area under the curve of MAC was 0.741.
Conclusions:
Complement 3, MAC, and MBL were significantly increased in septic patients with DIC. Membrane attack complex independently predicted sepsis-induced DIC and development of DIC after ED admission.
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