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Published on: September 15, 2023
The complement system is activated in a biphasic pattern after coronary artery bypass grafting
Cornelia Hoedemaekers1, Marcel van Deuren, Tom Sprong
1Department of Intensive Care, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands. C.Hoedemaekers@ic.umcn.nl
Insights
Complement activation after coronary artery bypass grafting (CABG) follows a biphasic pattern. Early activation involves classical and alternative pathways, while later stages show classical activation with engaged inhibitory mechanisms.
Area of Science:
- Immunology
- Cardiovascular Surgery
- Inflammation
Background:
- The complement system plays a crucial role in the inflammatory response post-coronary artery bypass grafting (CABG).
- Understanding the precise pathways of complement activation and deactivation after cardiac surgery remains unclear.
- This study aimed to elucidate the routes of complement activation following uncomplicated CABG.
Purpose of the Study:
- To analyze the specific pathways involved in complement activation after uncomplicated coronary artery bypass grafting.
- To investigate the temporal dynamics of complement activation and deactivation post-cardiac surgery.
Main Methods:
- Measurement of complement components and activation products in 20 adult patients undergoing elective CABG.
- Serial sampling from intensive care unit admission through postoperative recovery.
Main Results:
- Complement activation exhibited a biphasic pattern post-CABG.
- Initially (0-8 hours), activation involved classical/lectin and alternative pathways, leading to terminal complement complex formation.
- Later (post-8 hours), activation was primarily via the classical/lectin pathway without alternative pathway augmentation or terminal complex formation, suggesting engagement of inhibitory mechanisms.
Conclusions:
- Complement activation following cardiac surgery is a complex, biphasic process.
- Inhibitory mechanisms appear to be engaged approximately 8 hours postoperatively, modulating the complement response.
Background:
The complement system is a key component in the inflammatory response after coronary artery bypass grafting (CABG). The routes of complement activation and deactivation after cardiac surgery are not clear. The aim of this study was to analyze routes of complement activation after uncomplicated CABG.
Methods:
Complement components and activation products were measured in 20 nondiabetic adult patients undergoing elective CABG at several times postoperatively starting at admission to the intensive care unit.
Results:
Complement activation after uncomplicated CABG showed a biphasic pattern. In the first 8 hours after admission to the intensive care unit, complement activation was initiated by the classical lectin pathway and augmented by the alternative pathway. Ultimately, this resulted in terminal pathway activation and formation of terminal complement complex. In the second phase, starting at 8 hours after the operation, complement was still activated by the classical lectin pathway, but there was no augmentation by the alternative pathway and no terminal complement complex formation. This implies that during this second stage, inhibitory mechanisms beyond C3b are engaged.
Conclusions:
Complement activation after cardiac surgery is regulated in a complex biphasic way, with additional inhibitory mechanisms engaged from 8 hours postoperatively onward.
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