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.

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