Predictive value of anti-CarP and anti-PAD3 antibodies alone or in combination with RF and ACPA for the severity of rheumatoid arthritis.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
02 10 2021
Historique:
received: 30 04 2020
accepted: 14 12 2020
pubmed: 28 1 2021
medline: 22 12 2021
entrez: 27 1 2021
Statut: ppublish

Résumé

The objective of this study was to analyse the predictive value of anti-carbamylated protein (anti-CarP) and anti-peptidyl-arginine deiminase type-3 (anti-PAD3) antibodies, alone or in combination with RF and ACPA, to identify patients at high risk of developing severe RA outcomes. Patients within the Swiss Clinical Quality Management registry with a biobank sample were tested for RF, ACPA, anti-CarP, and anti-PAD3 antibodies. We examined the association of each autoantibody with DAS28, HAQ and radiographic damage (Ratingen) at baseline and longitudinally. Analyses included 851 established RA patients and 516 disease controls [axial spondyloarthritis (axSpA = 320) and PsA (196)]. Anti-CarP and anti-PAD3 antibodies were, respectively, present in 22.4% and 10.7% of the whole RA population, and in 13.2% and 3.8% of the RF and ACPA double seronegative patients. At baseline, RA patients with anti-PAD3 had higher DAS28 (4.2 vs 3.7; P= 0.005) and significantly more radiographic damage (14.9 vs 8.8; P= 0.02) than anti-PAD3-negative patients. In the ACPA-negative subgroup, baseline Ratingen scores were significantly higher in anti-PAD3-positive patients (P= 0.01). The combination of anti-PAD3, RF IgM, and ACPA was associated with significantly higher baseline radiographic scores than the double seropositive group (P= 0.04). The presence of any two of the previous autoantibodies was associated with significantly greater radiographic progression over 10 years than if all were absent (P= 0.02). There were no differences in RA outcome measures with regards to anti-CarP. Anti-PAD3 antibodies are associated with higher disease activity and joint damage scores in RA patients.

Identifiants

pubmed: 33502443
pii: 6121325
doi: 10.1093/rheumatology/keab050
doi:

Substances chimiques

Autoantibodies 0
PADI3 protein, human EC 3.5.3.15
Protein-Arginine Deiminase Type 3 EC 3.5.3.15

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4598-4608

Subventions

Organisme : De Reuter Foundation

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Celine Lamacchia (C)

Department of Rheumatology.

Matthias Jarlborg (M)

Department of Rheumatology.

Sylvette Bas (S)

Department of Rheumatology.

Pascale Roux-Lombard (P)

Department of Immunology and Allergy, Geneva University Hospital, Geneva.

Burkhard Möller (B)

Department of Rheumatology, Immunology and Allergy, Bern University Hospital, Bern.

Adrian Ciurea (A)

Department of Rheumatology, Zurich University Hospital, Zurich, Switzerland.

Axel Finckh (A)

Department of Rheumatology.

Chelsea Bentow (C)

Research and Development, Inova Diagnostics, San Diego, CA, USA.

Laura Martinez-Prat (L)

Research and Development, Inova Diagnostics, Barcelona, Spain.

Michael Mahler (M)

Research and Development, Inova Diagnostics, San Diego, CA, USA.

Cem Gabay (C)

Department of Rheumatology.

Michael J Nissen (MJ)

Department of Rheumatology.

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Classifications MeSH