Evidence map›Paper›PMID 39548536›Full record

ArticleJournal of translational medicine2024

Towards clinical translation of urinary vitronectin for non-invasive detection and monitoring of renal fibrosis in kidney transplant patients.

Marta Clos-Sansalvador, Omar Taco, Paula Rodríguez-Martínez, Sergio G Garcia, Miriam Font-Morón, Jordi Bover, Anna Vila-Santandreu, Marcella Franquesa, Javier Juega, Francesc E Borràs

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Article in Journal of translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

10 authors.

Marta Clos-Sansalvador *REMAR-IGTP Group, Germans Trias i Pujol Research Institute (IGTP) & , Nephrology Department, University Hospital Germans Trias i Pujol (HUGTiP) , Can Ruti Campus, Badalona (Barcelona), Catalonia, Spain.
Omar Taco *REMAR-IGTP Group, Germans Trias i Pujol Research Institute (IGTP) & , Nephrology Department, University Hospital Germans Trias i Pujol (HUGTiP) , Can Ruti Campus, Badalona (Barcelona), Catalonia, Spain.
Paula Rodríguez-MartínezDepartment of Pathology, University Hospital Germans Trias i Pujol, Badalona (Barcelona), Spain.
Sergio G GarciaREMAR-IGTP Group, Germans Trias i Pujol Research Institute (IGTP) & , Nephrology Department, University Hospital Germans Trias i Pujol (HUGTiP) , Can Ruti Campus, Badalona (Barcelona), Catalonia, Spain.
Miriam Font-MorónREMAR-IGTP Group, Germans Trias i Pujol Research Institute (IGTP) & , Nephrology Department, University Hospital Germans Trias i Pujol (HUGTiP) , Can Ruti Campus, Badalona (Barcelona), Catalonia, Spain.
Jordi BoverREMAR-IGTP Group, Germans Trias i Pujol Research Institute (IGTP) & , Nephrology Department, University Hospital Germans Trias i Pujol (HUGTiP) , Can Ruti Campus, Badalona (Barcelona), Catalonia, Spain.
Anna Vila-SantandreuREMAR-IGTP Group, Germans Trias i Pujol Research Institute (IGTP) & , Nephrology Department, University Hospital Germans Trias i Pujol (HUGTiP) , Can Ruti Campus, Badalona (Barcelona), Catalonia, Spain.
Marcella FranquesaREMAR-IGTP Group, Germans Trias i Pujol Research Institute (IGTP) & , Nephrology Department, University Hospital Germans Trias i Pujol (HUGTiP) , Can Ruti Campus, Badalona (Barcelona), Catalonia, Spain.
Javier JuegaREMAR-IGTP Group, Germans Trias i Pujol Research Institute (IGTP) & , Nephrology Department, University Hospital Germans Trias i Pujol (HUGTiP) , Can Ruti Campus, Badalona (Barcelona), Catalonia, Spain.
Francesc E BorràsREMAR-IGTP Group, Germans Trias i Pujol Research Institute (IGTP) & , Nephrology Department, University Hospital Germans Trias i Pujol (HUGTiP) , Can Ruti Campus, Badalona (Barcelona), Catalonia, Spain. feborras@igtp.cat.ORCID 0000-0003-4038-1912

Funding

Departament de Salut, Generalitat de Catalunya SLT017/20/000158FIPSE 4017-22HSRD VA HIR 10-001i-CERCA Ginjol 2022-10-001Instituto de Salud Carlos III FI20/00021Instituto de Salud Carlos III MS19/00018Instituto de Salud Carlos III PI19/00837'la Caixa' Foundation CI23-30015
6 · The paper itself

Abstract

backgroundInterstitial fibrosis and tubular atrophy (IFTA) is a critical factor in the prognosis of kidney health. Currently, IFTA quantitation in kidney biopsy samples is crucial for diagnosis and assessing disease severity, but the available non-invasive biomarkers are not satisfactory. Proteomic studies identified urinary vitronectin (VTN) as a potential biomarker for kidney fibrosis. As mass spectrometry techniques are not practical for use in clinical settings, we tested whether evaluation of urinary VTN levels through enzyme-linked immunosorbent assay (ELISA) can help monitor fibrotic changes in kidney transplant recipients and prove the clinical viability of the assay.

methodsA total of 58 kidney transplant (KTx) patients who underwent renal biopsy were included in the study. Patients were categorized into two groups referred as no fibrosis (0%) or with fibrosis (≥ 5%) based on their histological findings. In a subsequent/follow-up analysis, the time elapsed from transplantation was also considered. The urinary levels of VTN were measured using ELISA.

resultsVTN (p = 0.0180) and VTN normalized by urinary creatinine levels (p = 0.0037), were significantly increased in patients with fibrotic grafts. When focusing on patients with long-term grafts (> 3 years from transplantation, n = 36), VTN exhibited superior potential in identifying fibrotic grafts compared to albuminuria (VTN p = 0.0040 vs. albuminuria p = 0.0132). Importantly, in this group, while albuminuria correctly identified 71% of fibrotic patients, the combination of VTN plus albuminuria correctly classified 89% of fibrotic grafts detected by renal biopsy.

conclusionsVTN has emerged as a valid indicator of renal fibrosis. Of interest, urinary levels of VTN in combination with conventional clinical parameters (such as albuminuria) significantly improved the non-invasive detection of renal fibrosis in kidney transplant patients.

Indexed as

FibrosisKidneyKidney TransplantationVitronectinAdultBiomarkersBiopsyEnzyme-Linked Immunosorbent AssayFemaleHumansKidney DiseasesMaleMiddle AgedROC CurveTranslational Research, BiomedicalBiomarkersVitronectin(3–10): BiomarkerELISAExtracellular matrixKidney fibrosiskidney transplantLiquid biopsyNephrology

Identifiers

PMID39548536
PMCPMC11566717

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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.