Correlation between inflammatory response and markers of neuronal damage in coronary revascularization with and

Annamaria Mazzone1, Jacopo Gianetti, Eugenio Picano

  • 1Cardiac Surgery Department, CNR Institute of Clinical Physiology, Ospedale G. Pasquinucci, Massa, Italy. mazzone@ifc_cnr.pi.it

Perfusion
|April 23, 2003
PubMed

Insights

Off-pump coronary artery bypass graft (CABG) surgery demonstrates a reduced inflammatory response and neuronal damage compared to on-pump procedures. This study highlights the protective benefits of off-pump CABG in minimizing perioperative injury markers.

Area of Science:

  • Cardiovascular Surgery
  • Neuroscience
  • Immunology

Background:

  • Conventional coronary artery bypass graft (CABG) surgery utilizes cardiopulmonary bypass, which can trigger inflammatory responses and neuronal damage.
  • Off-pump CABG is a surgical technique that avoids cardiopulmonary bypass, potentially mitigating these adverse effects.

Purpose of the Study:

  • To investigate the protective effects of off-pump CABG surgery.
  • To compare plasma inflammatory and neuronal injury markers between on-pump and off-pump CABG procedures.

Main Methods:

  • A comparative study involving 41 patients undergoing elective CABG: 21 on-pump (Group I) and 20 off-pump (Group II).
  • Perioperative measurement of inflammatory markers: interleukin-2 receptor (IL-2r), interleukin-6 (IL-6), and tumor necrosis factor-alpha.
  • Perioperative measurement of neuronal injury markers: S-100 protein (S-100) and neuron-specific enolase (NSE).

Main Results:

  • Significantly lower postoperative peak values of NSE (p < 0.001) and S-100 (p < 0.05) were observed in the off-pump group (Group II).
  • Interleukin-6 (IL-6) levels were significantly lower in off-pump patients (p < 0.001).
  • A significant correlation was found between NSE and IL-6 levels (p < 0.001).

Conclusions:

  • Off-pump CABG surgery effectively reduces the inflammatory response during the perioperative period.
  • The technique also minimizes the release of neuronal damage markers, suggesting neuroprotective benefits.
  • The correlation between inflammatory markers and neuronal markers indicates a potential link between systemic inflammation and neuronal injury in CABG patients.