Abstract

BackgroundEnthesitis is a hallmark of spondyloarthritis (SpA) with a substantial impact on quality of life. Reports of treatment effectiveness across individual enthesitis sites in real-world patients with axial SpA (axSpA) are limited. We investigated the evolution of enthesitis following tumor necrosis factor inhibitor (TNFi) initiation in axSpA patients, both cumulatively and at specific axial and peripheral sites.MethodsAxSpA patients in the Swiss Clinical Quality Management Registry were included if they initiated a TNFi, had an available Maastricht Ankylosing Spondylitis Enthesitis Score, modified to include the plantar fascia (mMASES, 0–15), at start of treatment and after 6 and/or 12 months and ≥12 months follow-up. Logistic regression models were utilized to analyze explanatory variables for enthesitis resolution.ResultsOverall, 1668 TNFi treatment courses (TCs) were included, of which 1117 (67%) had active enthesitis at baseline. Reduction in mMASES at the 6- and 12-month timepoints was experienced in 72% and 70% of TCs, respectively. Enthesitis resolution at 6/12 months occurred in 37.9%/43.0% of all TNFi TCs and 40.7%/50.9% of first TNFi TCs. At 6 months, a significant reduction in the frequency of enthesitis was observed at all sites, except for the Achilles tendon and plantar fascia among first TNFi TCs, while at 12 months, reduction was significant at all sites in both TC groups. Enthesitis resolved in 60.3–77% across anatomical sites, while new incident enthesitis occurred in 4.0–13.5% of all TNFi TCs at 12 months. Both baseline and new-incident enthesitis occurred most frequently at the posterior superior iliac spine and the fifth lumbar spinous process. Younger age and lower mMASES at baseline were predictors of complete enthesitis resolution, while female sex and second- or later-line TNFi treatment were associated with persistence of enthesitis at 12 months.ConclusionIn real-world axSpA patients treated with a TNFi, enthesitis improved in the majority of patients across all anatomical sites. Significant improvement at the Achilles and plantar fascia entheses was observed only at 12 months. Complete and site-specific enthesitis resolution occurred in ≥40% and ≥60% of TCs evaluated at 12 months, with a low incidence of new site-specific enthesitis.Trial registrationNot applicable.

Highlights

  • Axial spondyloarthritis is an inflammatory rheumatic disease with a diverse clinical presentation [1, 2]

  • Of 3325 identified treatment courses (TCs) in 2130 patients with axial SpA (axSpA) who initiated tumor necrosis factor inhibitor (TNFi) therapy, 1668 TCs in 1393 patients met all 3 entry criteria of a Modified Maastricht Ankylosing Spondylitis Enthesitis Score (mMASES) available at baseline, at least another mMASES reported during followup, and available follow-up of at least 12 months (Fig. 1)

  • The median mMASES was 2 (IQR, 0–4) and 67% of TCs (1117 of 1668) were enthesitis positive at baseline; 23.5% were simultaneously co-treated with a csDMARD, and most TCs included patients receiving first-line TNFi therapy (62.7%)

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Summary

Introduction

Axial spondyloarthritis (axSpA) is an inflammatory rheumatic disease with a diverse clinical presentation [1, 2]. Extra-articular manifestations, such as acute anterior uveitis, psoriasis, and inflammatory bowel disease are characteristic of axSpA [1, 2]. AxSpA carries a significant patient burden and has a substantial impact on patients’ quality of life [1, 2, 5,6,7,8]. Enthesitis is a hallmark of spondyloarthritis (SpA) with a substantial impact on quality of life. Reports of treatment effectiveness across individual enthesitis sites in real-world patients with axial SpA (axSpA) are limited. We investigated the evolution of enthesitis following tumor necrosis factor inhibitor (TNFi) initiation in axSpA patients, both cumulatively and at specific axial and peripheral sites

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