A new serum biochemical marker of synovium turnover predicts radiographic progression in patients with early arthritis.

Rheumatoid arthritis biochemical marker collagen progression risk factor synovium

Journal

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

Informations de publication

Date de publication:
20 Jul 2023
Historique:
received: 09 03 2023
revised: 28 06 2023
accepted: 04 07 2023
medline: 20 7 2023
pubmed: 20 7 2023
entrez: 20 7 2023
Statut: aheadofprint

Résumé

To investigate whether serum Col 3-4, a new biochemical marker of synovial tissue turnover, was associated with progression of joint damage in patients with early arthritis. 788 early arthritis patients (<6-months symptoms, 82% diagnosis of RA, 18% undifferentiated arthritis) from the prospective ESPOIR study were investigated. Progression was defined as an increase of 1 or 5 unit(s) in radiographic van der Heijde modified Sharp score between baseline and 1 or 5 years, respectively. Associations between baseline Col 3-4 and progression were assessed by logistic regression. Each standard deviation increase of baseline Col 3-4 levels was associated with an increased 5-yr total damage progression with an odds-ratio (OR, 95 CI) of 1.51 (1.21-1.88), which remained significant when DAS28, C-reactive protein and anti-citrullinated protein antibodies positivity were included in the model [OR (95 CI): 1.34 (1.01-1.76)]. Further adjustment for bone erosion did not modify the association. Patients with both Col 3-4 in the highest quintile and bone erosion had a more than 2-fold higher risk of progression [OR (95 CI): 7.16 (2.31-22)] than patients with either high Col 3-4 [2.91 (1.79-4.73)] or bone erosion [2.36 (2.38-3.70)] alone. Similar associations were observed for prediction of 12 months progression. Increased serum Col 3-4 is associated with a higher risk of structural progression, independently of major risk factors. Col 3-4 may be useful in association with bone erosion to identify patients with early arthritis at higher risk.

Identifiants

pubmed: 37471609
pii: 7227067
doi: 10.1093/rheumatology/kead375
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2023. 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

Patrick Garnero (P)

INSERM, UMR1033, Hôpital Edouard Herriot, Pavillon F, Lyon, France.

Evelyne Gineyts (E)

INSERM, UMR1033, Hôpital Edouard Herriot, Pavillon F, Lyon, France.

Jean-Charles Rousseau (JC)

INSERM, UMR1033, Hôpital Edouard Herriot, Pavillon F, Lyon, France.

Pascal Richette (P)

Université Paris 7, UFR Médicale, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Lariboisière, Fédération de Rhumatologie, Paris, France.

Jérémie Sellam (J)

INSERM, UMRS 938, service de rhumatologie, Sorbonne Université, hôpital Saint-Antoine, AP-HP, Paris, France.

Roland Chapurlat (R)

INSERM, UMR1033, Hôpital Edouard Herriot, Pavillon F, Lyon, France.
Hospices Civils de Lyon, Hôpital Edouard Herriot, Lyon, France.

Classifications MeSH