Evidence map›Paper›PMID 39289297›Full record

ArticleJournal of nephrology2025

Gut mucosa alterations after kidney transplantation: a cross sectional study.

Rashmi Joshi, Carmine Secondulfo, Alessandro Caputo, Pio Zeppa, Candida Iacuzzo, Luca Apicella, Margherita Borriello, Giancarlo Bilancio, Davide Viggiano

Abstract read
In one paragraph

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

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Rashmi Joshi *Department of Translational Medical Sciences, University of Campania, Via Pansini, 5, 80131, Naples, Italy.
Carmine Secondulfo *Department of Medicine, Surgery and Dentistry, University of Salerno, Salerno, Italy.
Alessandro CaputoUnit of Pathology, University Hospital of Salerno, Salerno, Italy.
Pio ZeppaUnit of Pathology, University Hospital of Salerno, Salerno, Italy.
Candida IacuzzoUnit of Nephrology, Dialysis and Transplantation, University Hospital of Salerno, Salerno, Italy.
Luca ApicellaUnit of Nephrology, Dialysis and Transplantation, University Hospital of Salerno, Salerno, Italy.
Margherita BorrielloDepartment of Precision Medicine, University of Campania, Naples, Italy.
Giancarlo BilancioDepartment of Medicine, Surgery and Dentistry, University of Salerno, Salerno, Italy.
Davide ViggianoDepartment of Translational Medical Sciences, University of Campania, Via Pansini, 5, 80131, Naples, Italy. davide.viggiano@unicampania.it.ORCID http://orcid.org/0000-0002-2425-6057

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKidney transplant recipients (KTRs) rely on immunosuppressants like mycophenolate to prevent organ rejection. However, mycophenolate often causes intestinal symptoms and inflammation in various organs, including the skin and the colon. While KTRs have an increased risk for skin cancer, the risk of colorectal cancer is not increased. Elucidating the histological alterations in the colon of KTRs and comparing these changes with known skin alterations would help understand how immunosuppressants influence cancer development and progression.

methodsWhole slide images from gut biopsies (Non-transplanted subjects n = 35, KTRs n = 49) were analyzed using the ImageJ and R programming environment. A total of 22,035 epithelial cells, 38,870 interstitial cells, 3465 epithelial cell mitoses, and 7477 endothelial cells, each characterized by multiple microscopy parameters, from a total of 1788 glands were analyzed. The large database was subsequently analyzed to verify the changes of inflammatory milieu in KTRs and in cancer.

resultsKTRs without colon-cancer showed a significantly higher density of interstitial cells in the colon compared to non-transplanted patients. Moreover, the increase in interstitial cell number was accompanied by subtle modifications in the architecture of the colon glands, without altering the epithelial cell density. We could not identify significant structural modifications in cancer samples between KTRs and non-transplanted patients.

conclusionsOur findings demonstrate an increased number of resident interstitial cells in the colon of KTRs, as in other patients treated with mycophenolate. These changes are associated with subtle alterations in the architecture of colon glands.

Indexed as

ColonImmunosuppressive AgentsIntestinal MucosaKidney TransplantationAdultAgedBiopsyCross-Sectional StudiesFemaleHumansMaleMiddle AgedMycophenolic AcidImmunosuppressive AgentsMycophenolic AcidBiopsyGutImage analysisKidney transplant

Identifiers

PMID39289297
PMCPMC12187894

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