Complement component C5a predicts future cardiovascular events in patients with advanced atherosclerosis
Walter S Speidl1, Markus Exner, Jasmin Amighi
1Department of Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, A-1090 Vienna, Austria.
Insights
Elevated levels of complement component C5a predict cardiovascular risk in patients with advanced atherosclerosis. Measuring C5a may enhance risk prediction beyond traditional inflammatory markers.
Area of Science:
- Immunology
- Cardiovascular Medicine
- Biomarker Discovery
Background:
- Complement activation is implicated in atherosclerotic lesions.
- Complement component C5a has potent pro-inflammatory effects.
- The predictive value of plasma C5a for cardiovascular risk is unknown.
Purpose of the Study:
- To investigate if plasma C5a levels predict cardiovascular risk.
- To assess C5a's predictive value in patients with advanced atherosclerosis.
Main Methods:
- 173 patients with symptomatic peripheral artery disease were studied.
- Cardiovascular risk factors, C5a levels, and inflammatory markers were measured.
- Patients were followed for major adverse cardiovascular events (MACE).
Main Results:
- 65 MACE occurred in 49 patients (28%) over a median of 22 months.
- Higher C5a quartiles correlated with increased cumulative event rates (P=0.0077).
- Adjusted hazard ratios for MACE increased with C5a quartiles (P=0.038).
Conclusions:
- Elevated C5a is associated with increased cardiovascular risk in advanced atherosclerosis.
- C5a determination may improve cardiovascular risk prediction.
- C5a offers added predictive value beyond non-specific inflammatory markers.
Aims:
Complement activation occurs in atherosclerotic lesions, and particularly complement component C5a exerts potent chemotactic and proinflammatory effects. However, it is yet unknown, whether plasma levels of C5a may predict cardiovascular risk. The aim of this study was to examine whether plasma levels of the complement component C5a may predict cardiovascular risk in patients with advanced atherosclerosis.
Methods And Results:
We studied 173 patients with symptomatic peripheral artery disease (median age 72, 82 male). Cardiovascular risk profile, levels of the complement factor C5a, and other non-specific inflammatory parameters [high sensitivity C-reactive protein, serum amyloid A (SAA), and fibrinogen] were obtained at baseline, and patients were followed for median 22 months [interquartile range (IQR) 13-27] for the occurrence of major adverse cardiovascular events (MACE: myocardial infarction, percutaneous coronary interventions, coronary artery bypass graft, carotid revascularization, stroke, and death). We observed 65 MACE in 49 patients (28%). Cumulative event rates (95% confidence interval (CI)) within quartiles of C5a at 24 months were 16 (5-27), 26 (13-39), 36 (21-51), and 37% (23-51), respectively (P=0.0077). Adjusted hazard ratios for the occurrence of a first MACE according to increasing quartiles of C5a were 1.81, 2.23, and 2.66, respectively, as compared to the lowest quartile (P=0.038), irrespective of the level of other inflammatory parameters.
Conclusion:
Complement activation, indicated by the elevation of C5a, seems to be associated with increased cardiovascular risk in patients with advanced atherosclerosis. Clinically, determination of C5a may add to the predictive value of other non-specific inflammatory parameters.
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