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

antibodies against serine protease proteinase-3 disease severity health-related quality of life liver biochemistry primary sclerosing cholangitis survival

Journal

Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402

Informations de publication

Date de publication:
03 Nov 2022
Historique:
received: 20 07 2022
revised: 21 09 2022
accepted: 31 10 2022
entrez: 11 11 2022
pubmed: 12 11 2022
medline: 12 11 2022
Statut: epublish

Résumé

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.

Identifiants

pubmed: 36359524
pii: diagnostics12112682
doi: 10.3390/diagnostics12112682
pmc: PMC9689935
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Steffi Lopens (S)

Institute of Biotechnology, Faculty Environment and Natural Sciences, Brandenburg University of Technology Cottbus-Senftenberg, 01968 Senftenberg, Germany.
Medipan GmbH, 15827 Dahlewitz, Germany.

Ewa Wunsch (E)

Translational Medicine Group, Pomeranian Medical University in Szczecin, 70-204 Szczecin, Poland.

Malgorzata Milkiewicz (M)

Department of Medical Biology, Pomeranian Medical University in Szczecin, 70-204 Szczecin, Poland.

Nadja Röber (N)

Institute of Immunology, Technical University Dresden, 01069 Dresden, Germany.

Grit Zarske (G)

Medipan GmbH, 15827 Dahlewitz, Germany.

Abdullah Nasser (A)

Medipan GmbH, 15827 Dahlewitz, Germany.

Karsten Conrad (K)

Institute of Immunology, Technical University Dresden, 01069 Dresden, Germany.

Martin Laass (M)

Department of Pediatrics, Technical University Dresden, 01069 Dresden, Germany.

Stefan Rödiger (S)

Institute of Biotechnology, Faculty Environment and Natural Sciences, Brandenburg University of Technology Cottbus-Senftenberg, 01968 Senftenberg, Germany.
Faculty of Health Sciences Brandenburg, Brandenburg University of Technology Cottbus-Senftenberg, 01968 Senftenberg, Germany.

Marcin Krawczyk (M)

Department of Medicine II, Saarland University Medical Center, 66421 Homburg, Germany.
Laboratory of Metabolic Liver Diseases, Department of General, Transplant and Liver Surgery, Medical University of Warsaw, 02-097 Warsaw, Poland.
European Reference Network, 66421 Homburg, Germany.

Dirk Roggenbuck (D)

Institute of Biotechnology, Faculty Environment and Natural Sciences, Brandenburg University of Technology Cottbus-Senftenberg, 01968 Senftenberg, Germany.
Faculty of Health Sciences Brandenburg, Brandenburg University of Technology Cottbus-Senftenberg, 01968 Senftenberg, Germany.

Piotr Milkiewicz (P)

Translational Medicine Group, Pomeranian Medical University in Szczecin, 70-204 Szczecin, Poland.
Laboratory of Metabolic Liver Diseases, Department of General, Transplant and Liver Surgery, Medical University of Warsaw, 02-097 Warsaw, Poland.
European Reference Network, 02-097 Warsaw, Poland.

Classifications MeSH