Evidence map›Paper›PMID 36359524›Full record

ArticleDiagnostics (Basel, Switzerland)2022

PR3-ANCAs Detected by Third-Generation ELISA Predicts Severe Disease and Poor Survival in Primary Sclerosing Cholangitis.

Steffi Lopens, Ewa Wunsch, Malgorzata Milkiewicz, Nadja Röber, Grit Zarske, Abdullah Nasser, Karsten Conrad, Martin Laass, Stefan Rödiger, Marcin Krawczyk and 2 more

Open access · goldAbstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2022. 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
0.7field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

12 authors at 6 institutions in 2 countries.

Steffi LopensInstitute of Biotechnology, Faculty Environment and Natural Sciences, Brandenburg University of Technology Cottbus-Senftenberg, 01968 Senftenberg, Germany.
Ewa WunschTranslational Medicine Group, Pomeranian Medical University in Szczecin, 70-204 Szczecin, Poland.ORCID 0000-0001-8740-5243
Malgorzata MilkiewiczDepartment of Medical Biology, Pomeranian Medical University in Szczecin, 70-204 Szczecin, Poland.ORCID 0000-0002-2064-0545
Nadja RöberInstitute of Immunology, Technical University Dresden, 01069 Dresden, Germany.
Grit ZarskeMedipan GmbH, 15827 Dahlewitz, Germany.
Abdullah NasserMedipan GmbH, 15827 Dahlewitz, Germany.ORCID 0000-0001-8224-2326
Karsten ConradInstitute of Immunology, Technical University Dresden, 01069 Dresden, Germany.
Martin LaassDepartment of Pediatrics, Technical University Dresden, 01069 Dresden, Germany.ORCID 0000-0003-3670-3640
Stefan RödigerInstitute of Biotechnology, Faculty Environment and Natural Sciences, Brandenburg University of Technology Cottbus-Senftenberg, 01968 Senftenberg, Germany.ORCID 0000-0002-1441-6512
Marcin KrawczykDepartment of Medicine II, Saarland University Medical Center, 66421 Homburg, Germany.ORCID 0000-0002-0113-0777
Dirk RoggenbuckInstitute of Biotechnology, Faculty Environment and Natural Sciences, Brandenburg University of Technology Cottbus-Senftenberg, 01968 Senftenberg, Germany.ORCID 0000-0002-6861-6827
Piotr MilkiewiczTranslational Medicine Group, Pomeranian Medical University in Szczecin, 70-204 Szczecin, Poland.
Medipan (Germany) · DEBrandenburg University of Technology Cottbus-Senftenberg · DEMedical University of Warsaw · PLPomeranian Medical University · PLTechnische Universität Dresden · DEUniversity Hospital Carl Gustav Carus · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A highly sensitive detection of anti-neutrophil cytoplasmic antibodies to serine proteinase-3 (PR3-ANCAs) aids in the serological diagnosis of autoimmune liver disorders and the prediction of severity in primary sclerosing cholangitis (PSC). Here, we evaluate a novel third-generation ELISA for the detection of PR3-ANCAs. In total, 309 patients with PSC, 51 with primary biliary cholangitis (PBC), and 120 healthy blood donors (BD) were analyzed. For the survival analysis in PSC, the outcome was defined as liver-transplantation-free survival during the follow-up. Positive PR3-ANCA levels were found in 74/309 (24.0%) of patients with PSC. No BDs and one patient with PBC demonstrated PR3-ANCA positivity. PR3-ANCAs were revealed as independent predictors for a poor PSC outcome (study endpoint: liver transplantation/death, log-rank test, p = 0.02). PR3-ANCA positivity, lower albumin levels, and higher bilirubin concentrations were independent risks of a poor survival (Cox proportional-hazards regression analysis, p < 0.05). The Mayo risk score for PSC was associated with PR3-ANCA positivity (p = 0.01) and the disease severity assessed with a model of end-stage liver disease (MELD) and extended MELD-Na (p < 0.05). PR3-ANCAs detected by a third-generation ELISA are diagnostic and prognostic markers for PSC. Their wider use could help to identify patients who are at-risk of a more severe disease.

Indexed as

antibodies against serine protease proteinase-3disease severityhealth-related quality of lifeliver biochemistryprimary sclerosing cholangitissurvival

Identifiers

PMID36359524
PMCPMC9689935
OpenAlexW4308200861

What OpenQuestion holds

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LicenceCC BY
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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.