Alternative complement pathway activation during invasive coronary procedures in acute myocardial infarction and
Zsófia Horváth1, Dorottya Csuka2, Katarina Vargova3
1Research Group for Inflammation Biology and Immunogenomics of Hungarian Academy of Sciences and Semmelweis University, Róbert Károly krt. 44, 1134 Budapest, Hungary; Hungarian Defence Forces Medical Centre, Department of Cardiology, Róbert Károly krt. 44, 1134 Budapest, Hungary.
Insights
Percutaneous coronary procedures activate the alternative complement pathway, especially with contrast dye. In ST-elevation myocardial infarction, this pathway is already active before procedures.
Area of Science:
- Cardiovascular Medicine
- Immunology
- Interventional Cardiology
Background:
- The impact of percutaneous coronary procedures on complement activation remains unclear.
- Complement system activation is implicated in inflammatory responses and tissue injury.
Purpose of the Study:
- To investigate the effect of elective percutaneous coronary intervention (PCI) and diagnostic coronary angiography (CA) on complement activation.
- To compare complement activation in stable angina patients undergoing elective PCI (SA-PCI) versus ST-segment elevation myocardial infarction patients undergoing primary PCI (STEMI-PCI).
Main Methods:
- Measurement of complement activation products (C1rC1sC1inh, C3bBbP, SC5b-9) in SA-PCI (n=24), CA (n=52), and STEMI-PCI (n=23) patients.
- Blood samples collected at baseline, 6 hours, and 24 hours post-procedure.
- Correlation analysis between complement levels and clinical parameters (CK, creatinine, contrast volume).
Main Results:
- Elective PCI and CA induced a significant, reversible increase in the alternative pathway product C3bBbP 6 hours post-procedure (p<0.01).
- C3bBbP levels at 6 hours correlated with post-procedural CK, creatinine, and contrast volume.
- STEMI-PCI patients exhibited higher baseline C3bBbP and SC5b-9 levels compared to SA-PCI and CA patients (p<0.001 and p=0.011, respectively).
- Primary PCI in STEMI patients did not lead to further complement activation.
Conclusions:
- Elective coronary procedures trigger transient alternative complement pathway activation, influenced by contrast material volume.
- In STEMI, the alternative complement pathway is activated by the acute atherothrombotic event, with PCI having no additional detectable effect.
Abstract:
The effect of invasive percutaneous coronary procedures on complement activation has not been elucidated. We enrolled stable angina patients with elective percutaneous coronary intervention (SA-PCI, n=24), diagnostic coronary angiography (CA, n=52) and 23 patients with ST segment elevation myocardial infarction and primary PCI (STEMI-PCI). Complement activation products (C1rC1sC1inh, C3bBbP and SC5b-9) were measured on admission, 6 and 24h after coronary procedures. The alternative pathway product, C3bBbP significantly and reversibly increased 6h after elective PCI (baseline: 7.81AU/ml, 6h: 16.09AU/ml, 24h: 4.27AU/ml, p<0.01, n=23) and diagnostic angiography (baseline: 6.13AU/ml, 6h: 12.08AU/ml, 24h: 5.4AU/ml, p<0.01, n=52). Six hour C3bBbP values correlated with post-procedural CK, creatinine level and the applied contrast material volume (r=0.41, r=0.4, r=0.3, p<0.05, respectively). In STEMI-PCI, baseline C3bBbP level was higher, compared to SA-PCI or CA patients (11.33AU/ml vs. 7.81AU/ml or 6.13AU/ml, p<0.001). Similarly, the terminal complex (SC5b-9) level was already elevated at baseline compared to SA-PCI group (3.49AU/ml vs. 1.87AU/ml, p=0.011). Complement pathway products did not increase further after primary PCI. Elective coronary procedures induced transient alternative complement pathway activation, influenced by the applied contrast volume. In STEMI, the alternative complement pathway is promptly activated during the atherothrombotic event and PCI itself had no further detectable effect.
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