Cytochrome c in patients undergoing coronary artery bypass grafting: A post hoc analysis of a randomized trial

Lars W Andersen1, Xiaowen Liu2, Sophia Montissol2

  • 1Center for Resuscitation Science, Department of Emergency Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA; Research Center for Emergency Medicine, Aarhus University Hospital, Aarhus, Denmark.

Journal of Critical Care
|August 14, 2017
PubMed

Insights

Plasma cytochrome c is detectable in cardiac surgery patients but does not increase post-surgery. Cytochrome c levels showed no association with inflammation or clinical outcomes in this study.

Area of Science:

  • Cardiology
  • Biochemistry
  • Critical Care Medicine

Background:

  • Cardiac surgery can impact cellular function and stress markers.
  • Understanding the role of plasma cytochrome c in this context is crucial for patient monitoring.

Purpose of the Study:

  • To determine if plasma cytochrome c is detectable in patients undergoing cardiac surgery.
  • To investigate the association between cytochrome c levels and markers of cellular stress (lactate, inflammation, oxygen consumption).
  • To assess the relationship between cytochrome c levels and clinical outcomes after cardiac surgery.

Main Methods:

  • Observational sub-study within a randomized trial of thiamine vs. placebo in coronary artery bypass grafting patients.
  • Blood samples collected pre-surgery, post-surgery, and 6 hours post-surgery.
  • Measured plasma cytochrome c, inflammatory markers, and cellular oxygen consumption.

Main Results:

  • Cytochrome c was detectable in 98% of patients at baseline (median 0.18 ng/mL).
  • No significant changes in cytochrome c levels were observed from baseline to post-surgery or at 6 hours post-surgery.
  • Cytochrome c levels did not correlate with lactate, inflammatory markers, cellular oxygen consumption, or clinical outcomes.

Conclusions:

  • Plasma cytochrome c levels do not significantly increase following cardiac surgery.
  • Elevated cytochrome c is not associated with inflammation or poorer clinical outcomes in this patient cohort.
Abstract

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