Related Experiment Video
Updated: Feb 5, 2026

Optimized Management of Endovascular Treatment for Acute Ischemic Stroke
Published on: January 18, 2018
Complement Complex C5b-9 Levels Are Associated with the Clinical Outcomes of Acute Ischemic Stroke and Carotid Plaque
Weixin Si1, Pingping He1, Yi Wang1
1Department of Neurology, The Affiliated Shengjing Hospital of China Medical University, No. 36 Sanhao Street, Heping District, Shenyang, 110004, China.
Insights
Elevated levels of the terminal complement complex C5b-9 in acute ischemic stroke (AIS) patients correlate with stroke severity, poor outcomes, and unstable carotid plaques, suggesting it as a potential biomarker.
Area of Science:
- Immunology
- Neurology
- Cardiovascular Science
Background:
- The terminal complement complex C5b-9 is implicated in acute ischemic stroke (AIS) and carotid atherosclerosis.
- The relationship between serum C5b-9 levels, AIS severity, patient outcomes, and carotid plaque stability requires further investigation.
Purpose of the Study:
- To investigate the association between serum C5b-9 levels and the severity, outcome, and carotid plaque stability in patients with AIS.
Main Methods:
- Enzyme-linked immunosorbent assay (ELISA) was used to measure serum C5b-9 levels in 70 AIS patients and 70 healthy controls at 72 hours post-stroke.
- Evaluations included infarct size, National Institutes of Health Stroke Scale (NIHSS), 90-day modified Rankin Scale (mRS), and carotid plaque characteristics.
Main Results:
- Serum C5b-9 levels were significantly higher in AIS patients compared to controls (p < 0.001).
- C5b-9 levels correlated with infarct size (p = 0.045) and NIHSS scores (p = 0.035).
- Higher C5b-9 levels were observed in patients with poor 90-day outcomes (p < 0.001) and unstable carotid plaques (p = 0.009).
- Multivariate analysis identified C5b-9 as an independent risk factor for AIS (p < 0.001) and unstable carotid plaques (p = 0.015).
Conclusions:
- Serum C5b-9 may serve as a valuable biomarker for predicting AIS severity and patient outcomes.
- C5b-9 levels are associated with carotid plaque instability in AIS patients.
- These findings highlight the potential of C5b-9 as a therapeutic target in managing AIS and associated carotid atherosclerosis.
Abstract:
The terminal complement complex C5b-9 plays an important role in acute ischemic stroke (AIS) and carotid atherosclerosis. However, the associations between serum C5b-9, the severity and outcome of AIS, and the stability of carotid plaques have not been well investigated. In this clinical study, 70 patients with AIS and 70 healthy controls were enrolled. Serum C5b-9 levels at 72 h after stroke onset were measured by enzyme-linked immunosorbent assay (ELISA). Infarct size, the National Institutes of Health Stroke Scale (NIHSS), the 90-day modified Rankin Scale (mRS), and carotid plaque and stenosis were evaluated. Serum C5b-9 levels were significantly higher in AIS patients than in healthy controls (p < 0.001) and were correlated with infarction sizes (p = 0.045) and the NIHSS (P = 0.035). Furthermore, 90-day mRS analysis demonstrated that the patients with poor outcomes had higher serum C5b-9 levels than those with good outcomes (P < 0.001). Moreover, serum C5b-9 levels in AIS patients with unstable carotid plaques were much higher than in those with stable carotid plaques (P = 0.009). Multivariate logistic regression indicated that C5b-9 could be an independent risk factor for AIS (P < 0.001) and unstable carotid plaques (P = 0.015). Therefore, complement complex C5b-9 may be a potential biomarker in predicting the severity and outcome, as well as the stability of carotid plaques, in AIS patients.
Related Concept Videos
Complexation Equilibria: Factors Influencing Stability of Complexes
Acute Pancreatitis II: Clinical Manifestations and Management
Acute Coronary Syndrome II: Pathophysiology and Clinical Manifestations
Acute Kidney Injury III: Clinical Manifestations
Complement System
Complementation Tests
Organisms heterozygous for different mutations are crossed pairwise in all combinations. If present on different genes, the mutations can complement each other by providing the missing...

