Repurposing the Fibrosis-4 Score in Rheumatoid Arthritis: Data from the ESPOIR Cohort

Author:

Felten Renaud1ORCID,Fabacher Thibaut2,Sedmak Nathanaël2,Sibilia Jean1,Sordet Christelle1,Chatelus Emmanuel1,Berenbaum Francis3ORCID,Combe Bernard4,Ruyssen-Witrand Adeline5,Vittecoq Olivier6,Meyer Nicolas2ORCID,Gottenberg Jacques-Eric1

Affiliation:

1. National Reference Center for Rare Auto-Immune Diseasesest Sud-Ouest (RESO), Department of Rheumatology, Hôpitaux Universitaires de Strasbourg, 67091 Strasbourg, France

2. Department of Public Health, Hôpitaux Universitaires de Strasbourg, 67091 Strasbourg, France

3. Department of Rheumatology, INSERM, AP-HP Saint-Antoine Hospital, Sorbonne University, 75005 Paris, France

4. Faculty of Medicine, Montpellier University, 34090 Montpellier, France

5. Department of Rheumatology, Toulouse University Toulouse III Paul Sabatier, 31400 Toulouse, France

6. Department of Rheumatology & CIC-CRB1404, Rouen University Hospital, Normandie University, UNIROUEN, 76000 Rouen, France

Abstract

Background: We aimed to evaluate the value of the Fibrosis-4 (FIB-4) score as a prognostic factor in RA in the prospective ESPOIR cohort. Methods: We included patients from the ESPOIR cohort with a diagnosis of RA according to ACR/EULAR criteria. The formula for the FIB-4 score is as follows: [age (years) × aspartate transaminase level (U/L)]/[platelet count (109/L) × alanine aminotransferase level (U/L)1/2]. We used a linear mixed-effects model with a random effect of patient to account for repeated measures over time. Results: Overall, 647 of the 813 patients included met the ACR/EULAR criteria for RA, with no differential diagnosis during the first 10 years of follow-up. Of these patients, at baseline, 633 had a calculable FIB-4 score. Median FIB-4 score was 0.75 (interquartile range 0.53–0.99). On multivariate analysis, FIB-4 score was not independently associated with progression of Disease Activity Score in 28 joints over 10 years of follow-up, unlike baseline C-reactive protein level and SJC. Baseline FIB-4 score was not associated with the modified Sharp score at 5-year follow-up, unlike age and ACPAs. FIB-4 score was not associated with mortality (hazard ratio 1.1 [95% CI 0.46; 2.8], p = 0.77) or major adverse cardiovascular events (0.46 [0.13; 1.6], p = 0.22) over the 10-year follow-up. No significant change in FIB-4 score over time was related to treatments. Conclusions: The present prospective cohort study did not find a prognostic role of FIB-4 score in RA. Reassuringly, FIB-4 score was not increased with DMARD treatment after 10 years of follow-up.

Funder

Merck Sharp and Dohme

INSERM

The French Society of Rheumatology, Pfizer, Abbvie, Lilly, and more recently Fresenius and Galapagos

Publisher

MDPI AG

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