Pentraxin-3 dynamics during liver transplantation and association with early allograft dysfunction
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Published on: September 22, 2023
Alexandria Page1, Michael P Bokoch1, Dieter Adelmann1
1Department of Anesthesia and Perioperative Care, University of California San Francisco, San Francisco, CA, United States.
Introduction:
Liver transplantation involves significant Ischemia-Reperfusion Injury (IRI). Recipients frequently exhibit features of endothelial dysfunction, such as inflammation and coagulopathy, which may be associated with adverse outcomes, including early allograft dysfunction (EAD). Pentraxin-3 (PTX-3) is involved in vascular endothelial inflammation and dysfunction, and is synthesized by endothelial cells and leukocytes. In this retrospective cohort study, we hypothesized that PTX-3 levels are associated with EAD.
Methods:
PTX-3 levels were quantified in plasma samples collected during liver transplantation at the following time points: start of surgery (T1); end of liver dissection (T2); after reperfusion (T3 at 15 minutes; T4 60-120 minutes). Control samples from healthy living donors were collected at the start and end of surgery.
Results:
Plasma PTX-3 levels were higher during liver transplantation than in healthy controls at T1 (median 1.72 ng/mL, IQR 1.13-2.44 vs. 0.57 ng/mL, IQR 0.44-0.74), p<0.01, and increased over time in serial samples collected at T1, T3, and T4 (n = 50), p<0.001. In those who developed EAD, delta-PTX-3 after reperfusion (T3 to T4) was greater (median 12.3 ng/mL, IQR 6.65-18.7, n=17) compared to those without EAD (median 6.59 ng/mL, IQR 2.87-13.2, n=34), p=0.048, but there was no significant difference in final T4 PTX-3 levels. Delta-PTX-3 after reperfusion was greater in recipients of grafts that received normothermic machine perfusion (NMP) (median 12.7 ng/mL, IQR: 7.90-16.3, n=19), vs. Living Donor Liver Transplants (median 5.79ng/mL, IQR 2.60-10.2, n=24), p=0.02.
Discussion:
Circulating PTX-3 levels increased during liver transplantation, with the highest levels after reperfusion. This suggests IRI triggered an increase in PTX-3. After reperfusion, delta-PTX-3, but not final PTX-3, was associated with an increased incidence of EAD and was greatest in recipients of grafts after NMP, suggesting NMP may involve earlier activation of pathways downstream of IRI.
