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Original article
Functional limitations in the phase of clinically suspect arthralgia are as serious as in early clinical arthritis; a longitudinal study
  1. Robin M ten Brinck1,
  2. Hanna W van Steenbergen1,
  3. Lukas Mangnus1,
  4. Leonie E Burgers1,
  5. Monique Reijnierse2,
  6. Tom WJ Huizinga1 and
  7. Annette HM van der Helm-van Mil1
  1. 1 Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands
  2. 2 Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands
  1. Correspondence to Robin M ten Brinck; r.m.ten_brinck{at}lumc.nl

Abstract

Introduction A phase of arthralgia may precede the emergence of rheumatoid arthritis (RA). Although several studies have focused on biomarkers, the relevance of this phase for patients is less studied. It is unknown if patients already have functional limitations and if this is correlated to the extent of subclinical inflammation. Therefore, we assessed functional disability in patients with clinically suspect arthralgia (CSA), its association with MRI-detected subclinical inflammation and its course during progression to clinical arthritis.

Methods From April 2012 to March 2015, 241 patients had arthralgia for <1 year and were, based on clinical presentation, considered at risk for RA by their rheumatologists. At baseline, Health Assessment Questionnaire (HAQ) scores were determined and unilateral 1.5 T MRI of metacarpophalangeal, wrist and metatarsophalangeal joints were made. Presence of MRI-detected subclinical inflammation was assessed by summing synovitis, tenosynovitis and bone marrow oedema scores (range 0–189). Patients were followed on arthritis development and HAQ scores were repeated when clinical arthritis had developed.

Results The median HAQ score at presentation with CSA was 0.50. Higher MRI-inflammation scores were associated with higher HAQ scores (β=0.017, 95% CI=0.004 to 0.030). During median 103 weeks follow-up, 44 patients progressed to clinical arthritis. HAQ scores ≥1.0 were associated with arthritis development (HR=2.50, 95% CI=1.03 to 6.10). Within converters, median HAQ scores did not increase from presentation with CSA to arthritis development (0.88 and 0.75, p=0.36).

Conclusions HAQ scores ≥1.0 at presentation were associated with the development of clinical arthritis. Functional limitations in the prearthritis phase of CSA were as serious as in the early clinical phase, demonstrating the relevance of CSA from patients’ perspectives.

  • Rheumatoid Arthritis
  • Outcome Measures
  • Magnetic Resonance Imaging.

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

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Footnotes

  • Contributors RMtB and AHMvdH-vM contributed to the conception and study design. RMtB analysed the data. RMtB, HWvS, LM, LEB, MR, TWJH and AHMvdH-vM contributed to interpretation of the data. HWvS and LM contributed to acquisition of the data. RMtB and AHMvdH-vM wrote the first version of the manuscript and RMtB, HWvS, LM, LEB, MR, TWJH and AHMvdH-vM revised it critically. RMtB, HWvS, LM, LEB, MR, TWJH and AHMvdH-vM read and approved the final manuscript.

  • Funding This work was supported by the Dutch Arthritis Foundation and a Vidi grant by the Netherlands Organisation of Health Research and Development. The funding sources had no role in the design and conduct of the study; collection, management, analysis and interpretation of the data; preparation, review or approval of the manuscript or decision to submit the manuscript for publication.

  • Competing interests None declared.

  • Ethics approval The study was approved by the medical ethical committee of the Leiden University Medical Center. All patients signed informed consent.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data sharing statement No additional data are available.