Performance of an MRI scoring system for inflammation of joints and entheses in peripheral SpA: post-hoc analysis of the CRESPA trial

Abstract

Abstract Objectives The aim of this study was to investigate the reliability, validity, and sensitivity to change of a novel MRI scoring system in early peripheral SpA (pSpA). Methods MRI of the pelvis and lower extremities was performed before initiation of the TNF inhibitor golimumab in 56 patients and repeated in 46 patients who achieved sustained clinical remission after 24, 36 or 48 weeks. Three readers applied a semi-quantitative MRI scoring system for lower-extremity joint and entheseal inflammation. Four lesion types were assessed: entheseal osteitis, entheseal soft-tissue inflammation, joint osteitis, and joint synovitis/effusion. MRI response was defined as a decrease in MRI lower-extremity inflammation index (sum of scores from 75 sites, each scored 0–3) above the smallest detectable change (SDC). Results At follow-up, the MRI index decreased in 34 of 46 patients (74%), and 15 (33%) patients achieved MRI response, i.e. a decrease above SDC of 2.8. When restricting the analysis to patients with clinical involvement of lower-extremity sites that were assessed by MRI, 13 of 28 (46%) achieved MRI response. Interreader reliability was very good, with an average-measure intraclass correlation coefficient of 0.92 (95% CI: 0.85–0.95) for status scores and 0.89 (0.80–0.94) for change in scores. The MRI index correlated with other measures of disease activity, including CRP [Spearman’s rho 0.41 (0.23–0.56)], swollen joint count of 6 joints [0.47 (0.27–0.63)], tender enthesis count of 14 entheses [0.32 (0.12–0.50)] and pain score [0.28 (0.08–0.46)], all P < 0.05. Conclusion The proposed MRI lower-extremity inflammation index demonstrated reliability, validity, and sensitivity to change in patients with early pSpA. Trial registration Clinicaltrials.gov, http://clinicaltrials.gov, NCT01426815.