Evidence map›Paper›PMID 39936135›Full record

ArticleTransplantation direct2025

Additional Diagnoses Other Than Rejection in the Kidney Allograft Biopsy: Pitfalls for Biopsy-based Transcript Diagnostics.

Elena Rho, Lukas Weidmann, Raphael Korach, Nicola Bortel, Nicolas Schmid, Dusan Harmacek, Kai Castrezana Lopez, Britta George, Seraina von Moos, Birgit Maria Helmchen and 3 more

Abstract read
In one paragraph

Article in Transplantation direct, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Antibody-mediated rejection in ABO-incompatible kidney transplantation.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2026
    Article
  2. Article
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

13 authors.

Elena RhoDivision of Nephrology, University Hospital Zurich, Zürich, Switzerland.
Lukas WeidmannDivision of Nephrology, University Hospital Zurich, Zürich, Switzerland.
Raphael KorachDivision of Nephrology, University Hospital Zurich, Zürich, Switzerland.
Nicola BortelDivision of Nephrology, University Hospital Zurich, Zürich, Switzerland.
Nicolas SchmidDivision of Nephrology, University Hospital Zurich, Zürich, Switzerland.
Dusan HarmacekDivision of Nephrology, University Hospital Zurich, Zürich, Switzerland.
Kai Castrezana LopezDivision of Nephrology, University Hospital Zurich, Zürich, Switzerland.
Britta GeorgeDivision of Nephrology, University Hospital Zurich, Zürich, Switzerland.
Seraina von MoosDivision of Nephrology, Cantonal Hospital of Lucerne, Luzern, Switzerland.
Birgit Maria HelmchenDivision of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.
Ariana GaspertDivision of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.
Fabian RösslerDivision of Surgery and Transplantation, University Hospital Zurich, Zürich, Switzerland.
Thomas SchachtnerDivision of Nephrology, University Hospital Zurich, Zürich, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Biopsy-based transcripts associated with antibody-mediated rejection (AMR) hold promise as substitutes for C4d positivity. However, their utility in cases with additional diagnoses other than rejection remains inadequately studied. Methods: In our comprehensive analysis of 326 kidney allograft biopsies, assessed by histology and the Molecular Microscope Diagnostic System, we identified 68 cases characterized by additional pathologies, including pyelonephritis (n = 15), BK nephropathy (n = 20), acute interstitial nephritis (n = 5), and glomerular diseases (n = 28). Results: Among cases with pyelonephritis, 7 of 15 cases (46%) showed a rejection-like signal, 4 above (16%) and 3 (20%) below diagnostic thresholds. Notably, the T cell-mediated rejection (TCMR) archetype score R2 (median, 0.13; interquartile range [IQR], 0.04-0.34) predominantly contributed to this observation. In BK nephropathy, 13 of 20 cases (65%) showed a rejection-like signal, 10 (50%) above and 3 (15%) below diagnostic thresholds. Elevated TCMR R2 (median, 0.07; IQR, 0.00-0.41) and all AMR archetype scores R4-6 (median, 0.23; IQR, 0.07-0.53) were driving factors. Among cases with acute interstitial nephritis, 3 of 5 cases (60%) showed TCMR-like signal with elevated R2 scores (median, 0.13; IQR, 0.00-0.54). Conversely, only 5 of 28 cases (18%) showed a rejection-like signal in glomerular disease cases, whereas 57% displayed all AMR archetype scores of ≥0.30. Conclusions: Additional pathologies can affect the Molecular Microscope Diagnostic System output, giving a molecular rejection-like signal. The prevalence of rejection-like signals below diagnostic thresholds is noteworthy, warranting caution and prompting further investigation.

Identifiers

PMID39936135
PMCPMC11809974

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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.