Abstract

The initial management of rheumatoid arthritis (RA) has a high impact on disease prognosis. Therefore, we need to select the most appropriate treatment as soon as possible. This goal requires biomarkers of disease severity and prognosis. One such biomarker may be the presence of anti-carbamylated protein antibodies (ACarPA) because it is associated with adverse long term outcomes as radiographic damage and mortality. Here, we have assessed the ACarPA as short-term prognostic biomarkers. The study was conducted in 978 prospective early arthritis (EA) patients that were followed for two years. Our results show the association of ACarPA with increased levels of all the disease activity measures in the first visit after arthritis onset. However, the associations were more significant with the high levels in local measures of inflammation and physician assessment than with the increases in systemic inflammation and patient-reported outcomes. More notably, disease activity was persistently increased in the ACarPA positive patients during the two years of follow-up. These differences were significant even after accounting for the presence of other RA autoantibodies. Therefore, the ACarPA could be considered short-term prognostic biomarkers of increased disease activity in the EA patients.

Highlights

  • The initial management of rheumatoid arthritis (RA) has a high impact on disease prognosis

  • Median disease activity was moderate at onset (DAS28-erythrocyte sedimentation rate (ESR) = 4.4)

  • This reduction of the disease activity was reflected in the fraction of early arthritis (EA) patients with high disease activity (i.e., DAS28-ESR > 5.1): from 33.8% in the first visit to ≤ 9.2% in subsequent visits

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Summary

Introduction

The initial management of rheumatoid arthritis (RA) has a high impact on disease prognosis. The carbamylated proteins have undergone a posttranslational modification changing lysine to homocitrulline, which is structurally related to citrulline These antibodies have favorable characteristics as a potential biomarker in EA: their presence and specificity for RA are widely reproducible between laboratories and they are already present at arthritis o­ nset[13,14,15,16]. Regarding the short-term outcomes, the presence of ACarPA has been associated with higher disease activity (assessed with DAS28-ESR) at arthritis onset in several large EA c­ ohorts[18,22,23,24]. We have addressed the association of ACarPA with disease activity trying to clarify the value of ACarPA as short-term prognostic biomarkers at arthritis onset

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