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

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 d...

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Autores principales: Lopens, Steffi, Wunsch, Ewa, Milkiewicz, Malgorzata, Röber, Nadja, Zarske, Grit, Nasser, Abdullah, Conrad, Karsten, Laass, Martin, Rödiger, Stefan, Krawczyk, Marcin, Roggenbuck, Dirk, Milkiewicz, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689935/
https://www.ncbi.nlm.nih.gov/pubmed/36359524
http://dx.doi.org/10.3390/diagnostics12112682
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author Lopens, Steffi
Wunsch, Ewa
Milkiewicz, Malgorzata
Röber, Nadja
Zarske, Grit
Nasser, Abdullah
Conrad, Karsten
Laass, Martin
Rödiger, Stefan
Krawczyk, Marcin
Roggenbuck, Dirk
Milkiewicz, Piotr
author_facet Lopens, Steffi
Wunsch, Ewa
Milkiewicz, Malgorzata
Röber, Nadja
Zarske, Grit
Nasser, Abdullah
Conrad, Karsten
Laass, Martin
Rödiger, Stefan
Krawczyk, Marcin
Roggenbuck, Dirk
Milkiewicz, Piotr
author_sort Lopens, Steffi
collection PubMed
description 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.
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spelling pubmed-96899352022-11-25 PR3-ANCAs Detected by Third-Generation ELISA Predicts Severe Disease and Poor Survival in Primary Sclerosing Cholangitis Lopens, Steffi Wunsch, Ewa Milkiewicz, Malgorzata Röber, Nadja Zarske, Grit Nasser, Abdullah Conrad, Karsten Laass, Martin Rödiger, Stefan Krawczyk, Marcin Roggenbuck, Dirk Milkiewicz, Piotr Diagnostics (Basel) Article 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. MDPI 2022-11-03 /pmc/articles/PMC9689935/ /pubmed/36359524 http://dx.doi.org/10.3390/diagnostics12112682 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lopens, Steffi
Wunsch, Ewa
Milkiewicz, Malgorzata
Röber, Nadja
Zarske, Grit
Nasser, Abdullah
Conrad, Karsten
Laass, Martin
Rödiger, Stefan
Krawczyk, Marcin
Roggenbuck, Dirk
Milkiewicz, Piotr
PR3-ANCAs Detected by Third-Generation ELISA Predicts Severe Disease and Poor Survival in Primary Sclerosing Cholangitis
title PR3-ANCAs Detected by Third-Generation ELISA Predicts Severe Disease and Poor Survival in Primary Sclerosing Cholangitis
title_full PR3-ANCAs Detected by Third-Generation ELISA Predicts Severe Disease and Poor Survival in Primary Sclerosing Cholangitis
title_fullStr PR3-ANCAs Detected by Third-Generation ELISA Predicts Severe Disease and Poor Survival in Primary Sclerosing Cholangitis
title_full_unstemmed PR3-ANCAs Detected by Third-Generation ELISA Predicts Severe Disease and Poor Survival in Primary Sclerosing Cholangitis
title_short PR3-ANCAs Detected by Third-Generation ELISA Predicts Severe Disease and Poor Survival in Primary Sclerosing Cholangitis
title_sort pr3-ancas detected by third-generation elisa predicts severe disease and poor survival in primary sclerosing cholangitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689935/
https://www.ncbi.nlm.nih.gov/pubmed/36359524
http://dx.doi.org/10.3390/diagnostics12112682
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