Interpretation of DAS28 and its components in the assessment of inflammatory and non-inflammatory aspects of rheumatoid arthritis
- PMID: 30886959
- PMCID: PMC6390559
- DOI: 10.1186/s41927-018-0016-9
Interpretation of DAS28 and its components in the assessment of inflammatory and non-inflammatory aspects of rheumatoid arthritis
Abstract
Background: DAS28 is interpreted as the inflammatory disease activity of RA. Non-inflammatory pain mechanisms can confound assessment. We aimed to examine the use of DAS28 components or DAS28-derived measures that have been published as indices of non-inflammatory pain mechanisms, to inform interpretation of disease activity.
Methods: Data were used from multiple observational epidemiology studies of people with RA. Statistical characteristics of DAS28 components and derived indices were assessed using baseline and follow up data from British Society for Rheumatology Biologics Registry participants (1) commencing anti-TNF therapy (n = 10,813), or (2) changing between non-biologic DMARDs (n = 2992), (3) Early Rheumatoid Arthritis Network participants (n = 813), and (4) participants in a cross-sectional study exploring fibromyalgia and pain thresholds (n = 45). Repeatability was tested in 34 patients with active RA. Derived indices were the proportion of DAS28 attributable to patient-reported components (DAS28-P), tender-swollen difference and tender:swollen ratio. Pressure pain detection threshold (PPT) was used as an index of pain sensitisation.
Results: DAS28, tender joint count, visual analogue scale, DAS28-P, tender-swollen difference and tender:swollen ratio were more strongly associated with pain, PPT and fibromyalgia status than were swollen joint count or erythrocyte sedimentation rate. DAS28-P, tender-swollen difference and tender:swollen ratio better predicted pain over 1 year than did DAS28 or its individual components.
Conclusions: DAS28 is strongly associated both with inflammation and with patient-reported outcomes. DAS28-derived indices such as tender-swollen difference are associated with non-inflammatory pain mechanisms, can predict future pain and should inform how DAS28 is interpreted as an index of inflammatory disease activity in RA.
Conflict of interest statement
No additional ethical approvals were sought for this manuscript. The BSRBR cohorts were approved by NHS North West Multicentre Research Ethics Committee (00/8/53). ERAN was approved by Trent Research Ethics Committee (01/4/047). The hospital-based study of pain pressure thresholds and pain mechanisms in people with RA were approved by the East Midlands NREC – Nottingham 2 (13/EM/0047). Written informed consent was obtained from all study participants.None was required.DFM and DAW declare grant support from Pfizer Ltd (iCRP scheme; grant #WI190792). DAW has undertaken paid consultancy, outside of this work, for Pfizer Ltd. and GSK Consumer Healthcare.Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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