Abstract

BackgroundSerum levels of calprotectin, a major S100 leucocyte protein, are associated with disease activity in rheumatoid arthritis (RA) and psoriatic arthritis (PsA) patients. Higher drug trough serum levels are associated with good response in patients treated with tumour necrosis factor inhibitors (TNFi). Power Doppler ultrasound (PDUS) synovitis is predictive of flare and progression of structural damage in patients in clinical remission. The purpose of this study was to analyse the accuracy of calprotectin and TNFi trough serum levels in detecting PDUS synovitis in RA and PsA patients in clinical remission or with low disease activity who were receiving TNFi.MethodsWe conducted a cross-sectional study of 92 patients (42 with RA, 50 with PsA) receiving adalimumab (ADA), etanercept (ETN) or infliximab who were in remission or had low disease activity (28-joint Disease Activity Score based on erythrocyte sedimentation rate <3.2). Associations of calprotectin, TNFi trough serum levels and acute phase reactants with PDUS synovitis were assessed using correlation and linear regression analyses. The accuracy and discriminatory capacity in detecting PDUS synovitis was assessed using ROC curves.ResultsPDUS synovitis was found in 62.4 % of RA patients and 32 % of PsA patients. Both RA and PsA patients with PDUS synovitis had higher calprotectin levels and lower TNFi trough serum levels. Calprotectin positively correlated with ultrasound scores (all r coefficients >0.50 in RA). Calprotectin correlated with the PDUS synovitis score in patients treated with ADA and ETN. Using PDUS synovitis (yes or no) as the reference variable, calprotectin had an AUC of 0.826. The best cut-off was ≥1.66 μg/ml, with a likelihood ratio of 2.77. C-reactive protein (AUC 0.673) and erythrocyte sedimentation rate (AUC 0.731) had a lower discriminatory capacity. TNFi trough serum levels were significantly associated with PDUS synovitis (OR 0.67, 95 % CI 0.52–0.85, p < 0.001) but their accuracy (AUC <0.5) was less than that of calprotectin. TNFi trough serum levels were inversely correlated with calprotectin and PDUS synovitis in RA and PsA patients receiving ADA and ETN.ConclusionsCalprotectin and TNFi trough serum levels may help identify PDUS synovitis in RA and PsA patients in clinical remission or with low disease activity.

Highlights

  • Serum levels of calprotectin, a major S100 leucocyte protein, are associated with disease activity in rheumatoid arthritis (RA) and psoriatic arthritis (PsA) patients

  • Calprotectin and tumour necrosis factor inhibitors (TNFi) trough serum levels may help identify Power Doppler ultrasound (PDUS) synovitis in RA and PsA patients in clinical remission or with low disease activity

  • All patients were in remission (28-joint Disease Activity Score based on erythrocyte sedimentation rate [DAS28ESR] ≤2.6) or had low disease activity (DAS28-ESR ≤3.2) in two consecutive visits ≥3 months apart and had been taking adalimumab (ADA), etanercept (ETN) or infliximab (IFX) for ≥3 months

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Summary

Introduction

A major S100 leucocyte protein, are associated with disease activity in rheumatoid arthritis (RA) and psoriatic arthritis (PsA) patients. The purpose of this study was to analyse the accuracy of calprotectin and TNFi trough serum levels in detecting PDUS synovitis in RA and PsA patients in clinical remission or with low disease activity who were receiving TNFi. New therapeutic strategies, including early therapy, treatto-target approaches and biological therapies, have led to substantial improvements in the prognosis of patients with rheumatoid arthritis (RA) and other types of inflammatory arthritis, such as ankylosing spondylitis and psoriatic arthritis (PsA) [1]. MSUS has revealed that a significant proportion of patients classified as being in clinical remission exhibit power Doppler ultrasound (PDUS) synovitis, which may explain the joint damage progression observed in some patients despite no clinical findings of disease activity. PDUS synovitis is predictive of clinical flares [12,13,14,15]

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