Evidence map›Paper›PMID 37020541›Full record

ArticleFrontiers in immunology2023

Biomarkers of fibrosis, kidney tissue injury and inflammation may predict severity and outcome of renal ANCA - associated vasculitis.

Veronika Satrapova, Nadja Sparding, Federica Genovese, Morten Asser Karsdal, Lenka Bartonova, Doubravka Frausova, Eva Honsova, Marek Kollar, Miloslav Suchanek, Helena Koprivova and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.1field-weighted citation impact, top 6% of its field
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

11 citing papers in PubMed, 16 citations in OpenAlex.

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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

14 authors at 5 institutions in 2 countries.

Veronika SatrapovaDepartment of Nephrology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czechia.
Nadja SpardingNordic Bioscience, Herlev, Denmark.
Federica GenoveseNordic Bioscience, Herlev, Denmark.
Morten Asser KarsdalNordic Bioscience, Herlev, Denmark.
Lenka BartonovaDepartment of Pathology, Institute for Clinical and Experimental Medicine, Prague, Czechia.
Doubravka FrausovaDepartment of Nephrology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czechia.
Eva HonsovaDepartment of Pathology, Institute for Clinical and Experimental Medicine, Prague, Czechia.
Marek KollarDepartment of Pathology, Institute for Clinical and Experimental Medicine, Prague, Czechia.
Miloslav SuchanekFaculty of Environment, Jan Evangelista Purkyně University in Ústí nad Labem, Ústí nad Labem, Czechia.
Helena KoprivovaInstitute of Medical Biochemistry and Laboratory Diagnostics, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czechia.
Romana RysavaDepartment of Nephrology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czechia.
Vladimira BednarovaDepartment of Nephrology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czechia.
Vladimir TesarDepartment of Nephrology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czechia.
Zdenka HruskovaDepartment of Nephrology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czechia.
General University Hospital in Prague · CZCharles University · CZInstitute of Clinical and Experimental Medicine · CZNordic Bioscience (Denmark) · DKJan Evangelista Purkyně University in Ústí nad Labem · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Activity and chronicity of kidney involvement in ANCA-associated vasculitis (AAV) can be currently reliably evaluated only by kidney biopsy. In this study, we measured a panel of serum and urinary biomarkers collected at the time of kidney biopsy and hypothesized that they could reflect specific histopathological parameters in the biopsy and help to predict prognosis. Methods: We examined a cohort of 45 patients with AAV and 10 healthy controls. Biomarker levels (DKK-3, CD163, EGF, PRO-C6 and C3M) were measured in this study by ELISA. Biopsies were scored with a scoring system for AAV (focal x crescentic x sclerotic x mixed class) and interstitial fibrosis was quantified. Results: Levels of urinary DKK-3, CD163, EGF, PRO-C6 and C3M significantly differed among biopsy classes in AAV, with urinary DKK-3 and PRO-C6 levels being highest in the sclerotic class and lowest in the focal class, urinary CD163 levels highest in the crescentic class and urinary C3M levels highest in the focal class. Moreover, the urinary biomarkers were able to discriminate focal biopsy class from the other classes. Urinary DKK-3, EGF, PRO-C6 and C3M levels measured at the time of biopsy were also significantly related to the extent of fibrosis and to the final kidney function at the end of follow-up. Conclusions: This small pilot study suggests that selected urinary biomarkers of fibrosis and inflammation may reflect changes in the kidney biopsy and be prognostic of kidney outcome in patients with AAV.

Indexed as

Antibodies, Antineutrophil CytoplasmicAnti-Neutrophil Cytoplasmic Antibody-Associated VasculitisBiomarkersEpidermal Growth FactorFibrosisHumansInflammationKidneyPilot ProjectsAntibodies, Antineutrophil CytoplasmicBiomarkersEpidermal Growth FactorANCA- associated vasculitisbiomarkerschronic kidney diseaseDKK-3kidney biopsykidney fibrosisPRO-C6

Identifiers

PMID37020541
PMCPMC10067901
OpenAlexW4327979162

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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 OpenQuestion graph.