Spondyloarthritis & psoriatic arthritis

Association of nociplastic and neuropathic pain components with the presence of residual symptoms in patients with axial spondyloarthritis receiving biological disease-modifying antirheumatic drugs

RMD OpenPublished Cross-sectional analysis of a prospective inception cohort

An erratum to this article was published (RMD Open, 4 Apr 2024 ↗)

Authors' conclusion

Both NoP and NP components seem to be associated with residual symptoms in patients with r-axSpA receiving treatment with bDMARDs.

Study context

Population
Patients with radiographic axial spondyloarthritis (r-axSpA) from the GErman SPondyloarthritis Inception Cohort receiving a bDMARD for at least 3 months
Participants
78 patients
Outcome
Association of nociplastic (NoP) (WPI) and neuropathic pain (NP) (PainDETECT) components with residual symptoms (ASDAS, BASDAI)
Methodological detailsunivariable and multivariable regression, cluster analysis
  • Univariable and multivariable regression
  • Cluster analysis

Main finding

As reported in the abstract

Widespread Pain Index (WPI) with Axial Spondyloarthritis Disease Activity Score (ASDAS), b

0.1 (0.04 to 0.17) (95% CI)

PainDETECT (PD) with ASDAS, b

0.05 (0.02 to 0.08) (95% CI)

WPI with Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), b

0.24 (0.08 to 0.39) (95% CI)

PD with BASDAI, b

0.17 (0.1 to 0.25) (95% CI)

Observational data: associations, not effects.

Further findings

Relevant residual symptoms (BASDAI ≥4)

WPI, OR
1.93 (1.09 to 4.15) (95% CI)
PD, OR
1.32 (1.04 to 1.85) (95% CI)

Patients with normal C reactive protein (CRP)

The effects were present also in patients with normal level of CRP

Cluster analysis

Distinct pain distribution profiles
3
Specific sensory symptom constellations
4

Original publication

Association of nociplastic and neuropathic pain components with the presence of residual symptoms in patients with axial spondyloarthritis receiving biological disease-modifying antirheumatic drugs. RMD Open. Published 15 February 2024. doi:10.1136/rmdopen-2023-004009

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