# Soluble Thrombomodulin as a Marker of Endothelial Injury in Early Post-Transplant Period: A Comparative Study of Simple Hypothermia and Pulsatile Machine Perfusion in Kidney Graft Preservation

**Authors:** Maciej Kotowski, Anna Prekwa, Adam Nowacki, Iga Stukan, Karol Tejchman, Jerzy Sieńko, Przemysław Nowacki, Bogusław Machaliński, Marek Ostrowski

PMC · DOI: 10.3390/jcm15010269 · Journal of Clinical Medicine · 2025-12-29

## TL;DR

This study explores how different kidney preservation methods affect endothelial injury after transplantation by measuring soluble thrombomodulin levels in the early post-transplant period.

## Contribution

The study introduces a novel paired-kidney design to compare endothelial injury markers during reperfusion using different preservation techniques.

## Key findings

- sTM levels decreased significantly in the HMP group between 1 and 30 minutes post-reperfusion.
- Early graft function improved in both groups with no significant inter-group differences.
- No cases of delayed graft function or graft thrombosis were observed in either group.

## Abstract

Background: Ischemia–reperfusion injury is a major contributor to early graft dysfunction after kidney transplantation and is associated with endothelial damage, reflected by circulating soluble thrombomodulin (sTM). This exploratory study aimed to assess very early graft-level changes in renal vein sTM during reperfusion using a paired-kidney design, in which kidneys from the same donor were preserved using different strategies: static cold storage (SCS) and hypothermic machine perfusion (HMP). Methods: Renal vein blood samples were collected intraoperatively at 1 and 30 min after reperfusion. Plasma sTM concentrations were determined using ELISA. Early graft function was monitored during the first 7 days post-transplantation. Results: Cold ischemia time was longer in the HMP group than in the SCS group (20 ± 8 h vs. 13 ± 6 h, p < 0.05). At 1 min post-reperfusion, sTM levels were comparable between groups. In the HMP group, sTM decreased significantly between 1 and 30 min after reperfusion, whereas no change was observed in the SCS group. Between-group differences at either time point did not reach statistical significance. Early renal function parameters improved in both groups, with no significant inter-group differences. No cases of delayed graft function or graft thrombosis occurred. Conclusions: Kidney preservation strategy may modulate very early graft-level endothelial responses during reperfusion, reflected by renal vein sTM dynamics. Although a limited sample size may have reduced the ability to detect between-group differences, very early renal vein sTM measurements may provide insight into ischemia–reperfusion injury. Clinical relevance requires validation in larger studies.

## Full-text entities

- **Genes:** THBD (thrombomodulin) [NCBI Gene 7056] {aka AHUS6, BDCA-3, BDCA3, CD141, THPH12, THRM}
- **Diseases:** endothelial damage (MESH:D014652), Ischemia (MESH:D007511), thrombosis (MESH:D013927), reperfusion injury (MESH:D015427), Hypothermia (MESH:D007035)

## Full text

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## Figures

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## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12787036/full.md

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Source: https://tomesphere.com/paper/PMC12787036