Evidence map›Paper›PMID 41661383›Full record

ReviewClinical and experimental nephrology2026

Exfoliated kidney cells from urine for non-invasive kidney transplant monitoring: A potential opportunity?

Henry H L Wu, Naveen Kumar Parthiban, Ewa M Goldys, Carol A Pollock, Sonia Saad

Abstract readReview
In one paragraph

Review in Clinical and experimental nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

5 authors.

Henry H L WuRenal Research, Kolling Institute of Medical Research, Royal North Shore Hospital and The University of Sydney, Kolling Building, St. Leonards, Sydney, NSW, 2065, Australia. honlinhenry.wu@health.nsw.gov.au.ORCID http://orcid.org/0000-0002-4561-0844
Naveen Kumar ParthibanRenal Research, Kolling Institute of Medical Research, Royal North Shore Hospital and The University of Sydney, Kolling Building, St. Leonards, Sydney, NSW, 2065, Australia.
Ewa M GoldysARC Centre of Excellence for Nanoscale Biophotonics, School of Biomedical Engineering, The University of New South Wales, Sydney, Australia.
Carol A PollockRenal Research, Kolling Institute of Medical Research, Royal North Shore Hospital and The University of Sydney, Kolling Building, St. Leonards, Sydney, NSW, 2065, Australia.
Sonia SaadRenal Research, Kolling Institute of Medical Research, Royal North Shore Hospital and The University of Sydney, Kolling Building, St. Leonards, Sydney, NSW, 2065, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kidney transplantation is usually the optimal treatment option for patients living with kidney failure given its associations with improved survival, quality of life outcomes and a reduction in the personal, economic, and societal burden of long-term dialysis. While advantages of kidney transplantation are recognized, post-transplant complications, such as graft rejection, ischemia-reperfusion injury, surgical-related complications, and long-term consequences of immunosuppressive therapies, are commonly observed. There has been increased research on developing non-invasive biomarkers for the monitoring of transplanted kidneys over recent decades. The potential of urinary biomarkers to identify graft rejection, post-transplant acute tubular necrosis, detect progression of epithelial-to-mesenchymal transition toward tubulointerstitial fibrosis, and to differentiate between causes of graft dysfunction is an attractive alternative to invasive transplant biopsy. Innovative urinary biomarkers, such as those derived from omics technologies allow for a more holistic assessment of graft status through multi-parametric molecular analysis, although there remain questions on the consistency, reliability, and practicality of utilizing omics-based urinary biomarkers. The international nephrology community has continued to make concerted efforts to improve the procedures and cost-effectiveness of kidney transplant monitoring. In this article, we review the evidence and limitations of currently available urinary biomarkers and propose the application of urine-derived exfoliated kidney cells such as urinary exfoliated proximal tubule cells to prognosticate kidney transplant outcomes and monitor for post-transplant complications. Artificial intelligence and the incorporation of machine learning analysis of proximal tubular cell characteristics may optimize the process of differentiating graft rejection from other forms of kidney dysfunction non-invasively following kidney transplantation.

Indexed as

Graft RejectionKidneyKidney TransplantationBiomarkersHumansPredictive Value of TestsTreatment OutcomeBiomarkersKidney transplantationNon-invasiveTransplant monitoringUrinary biomarkersUrinary exfoliated kidney cells

Identifiers

PMID41661383
PMCPMC13242432

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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 OpenQuestion graph.