Evidence map›Paper›PMID 40650073›Full record

ArticleInternational journal of molecular sciences2025

Metabolomic Insight into Donation After Circulatory-Death Kidney Grafts in Porcine Autotransplant Model: Normothermic Ex Vivo Kidney Perfusion Compared with Hypothermic Machine Perfusion and Static Cold Storage.

Iga Stryjak, Natalia Warmuzińska, Kamil Łuczykowski, Kacper Wnuk, Hernando Rosales-Solano, Patrycja Janiszek, Peter Urbanellis, Katarzyna Buszko, Janusz Pawliszyn, Markus Selzner and 1 more

Abstract readComparative Study
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Iga StryjakDepartment of Pharmacodynamics and Molecular Pharmacology, Faculty of Pharmacy, Nicolaus Copernicus University in Torun, Collegium Medicum in Bydgoszcz, 85-089 Bydgoszcz, Poland.
Natalia WarmuzińskaDepartment of Pharmacodynamics and Molecular Pharmacology, Faculty of Pharmacy, Nicolaus Copernicus University in Torun, Collegium Medicum in Bydgoszcz, 85-089 Bydgoszcz, Poland.ORCID 0000-0003-3418-9692
Kamil ŁuczykowskiDepartment of Pharmacodynamics and Molecular Pharmacology, Faculty of Pharmacy, Nicolaus Copernicus University in Torun, Collegium Medicum in Bydgoszcz, 85-089 Bydgoszcz, Poland.ORCID 0000-0001-7254-0864
Kacper WnukDepartment of Biostatistics and Biomedical Systems Theory, Faculty of Pharmacy, Nicolaus Copernicus University in Torun, Collegium Medicum in Bydgoszcz, 85-089 Bydgoszcz, Poland.ORCID 0000-0002-8301-2634
Hernando Rosales-SolanoDepartment of Chemistry, University of Waterloo, Waterloo, ON N2L 3G1, Canada.
Patrycja JaniszekDepartment of Pharmacodynamics and Molecular Pharmacology, Faculty of Pharmacy, Nicolaus Copernicus University in Torun, Collegium Medicum in Bydgoszcz, 85-089 Bydgoszcz, Poland.
Peter UrbanellisAjmera Transplant Center, Department of Surgery, Toronto General Hospital, University Health Network, Toronto, ON M5G 2N2, Canada.
Katarzyna BuszkoDepartment of Biostatistics and Biomedical Systems Theory, Faculty of Pharmacy, Nicolaus Copernicus University in Torun, Collegium Medicum in Bydgoszcz, 85-089 Bydgoszcz, Poland.ORCID 0000-0003-0388-3446
Janusz PawliszynDepartment of Chemistry, University of Waterloo, Waterloo, ON N2L 3G1, Canada.
Markus SelznerAjmera Transplant Center, Department of Surgery, Toronto General Hospital, University Health Network, Toronto, ON M5G 2N2, Canada.
Barbara BojkoDepartment of Pharmacodynamics and Molecular Pharmacology, Faculty of Pharmacy, Nicolaus Copernicus University in Torun, Collegium Medicum in Bydgoszcz, 85-089 Bydgoszcz, Poland.ORCID 0000-0003-3971-9816

Funding

National Science Center 2017/27/B/NZ5/01013
6 · The paper itself

Abstract

Organ shortage is a major challenge in transplantation, prompting the use of extended criteria donor grafts. These require improved preservation techniques and reliable methods to assess graft function. This study aimed to evaluate changes in the kidney metabolome following three preservation methods: normothermic ex vivo kidney perfusion (NEVKP), hypothermic machine perfusion (HMP) and static cold storage (SCS) in porcine autotransplant models. A chemical biopsy allowed minimally invasive sampling of metabolites, which were analyzed using liquid chromatography coupled with high-resolution mass spectrometry. The results highlighted metabolites affected by ischemia and oxidative stress in donor kidneys, as well as changes specific to each preservation method. Differences were observed immediately after transplantation and reperfusion and several days post-surgery. NEVKP was associated with the activation of physiological anti-oxidative and anti-inflammatory mechanisms, suggesting potential protective effects. However, some metabolites had dual roles, which may influence future graft treatment designs. HMP and SCS, while reducing energy demand in cells, also limit physiological repair mechanisms. These findings provide a basis for improving graft assessment and organ preservation, with chemical biopsy serving as both a tool for discovery and a potential diagnostic method for monitoring graft quality.

Indexed as

KidneyKidney TransplantationMetabolomeMetabolomicsOrgan PreservationPerfusionAnimalsCryopreservationSwineTissue DonorsTransplantation, Autologousgraft quality assessmentkidney perfusionkidney transplantationLC–MSliquid chromatography–mass spectrometrymetabolomicssolid-phase microextraction SPME

Identifiers

PMID40650073
PMCPMC12249885

What Socratic holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.