Evidence map›Paper›PMID 38508678›Full record

ArticleRMD open2024

Pain sensitisation and joint inflammation in patients with active rheumatoid arthritis.

Khaldoun Chaabo, Estee Chan, Toby Garrood, Zoe Rutter-Locher, Alex Vincent, James Galloway, Sam Norton, Bruce W Kirkham

Abstract read
In one paragraph

Article in RMD open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Towards an individualised approach to pain management in inflammatory arthritis.Therapeutic advances in musculoskeletal disease · 2026
    Review
  8. Article
  9. Article
  10. Review
  11. Observational
  12. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Khaldoun ChaaboRheumatology, Guy's and St Thomas' Hospitals NHS Trust, London, UK.
Estee ChanRheumatology, Guy's and St Thomas' Hospitals NHS Trust, London, UK.
Toby GarroodRheumatology, Guy's and St Thomas' Hospitals NHS Trust, London, UK.
Zoe Rutter-LocherRheumatology, Guy's and St Thomas' Hospitals NHS Trust, London, UK.ORCID 0000-0001-8251-4037
Alex VincentGuy's and St Thomas' Hospitals NHS Trust, London, UK.
James GallowayAcademic Department of Rheumatology, King's College London, London, UK.
Sam NortonAcademic Department of Rheumatology, King's College London, London, UK.ORCID 0000-0003-1714-9963
Bruce W KirkhamRheumatology, Guy's and St Thomas' Hospitals NHS Trust, London, UK bruce.kirkham@gstt.nhs.uk.ORCID 0000-0002-5110-3320

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDespite better therapies and strategies, many people with rheumatoid arthritis (RA) have persistent pain, often from abnormal pain processing, now termed nociplastic pain. However, RA patients with fibromyalgia (FM), a central nociplastic pain syndrome, also have power doppler ultrasound (PDUS+) joint inflammation. To understand the complex causes of pain, we performed clinical examination and patient-reported outcome measures (PROMs) plus comprehensive PDUS evaluation not previously combined.

methodsIn a cross-sectional study of sequential RA patients with at least moderate DAS28 erythrocyte sedimentation rate disease activity, we assessed 66/68 joints for swelling and tenderness, respectively, FM American College of Rheumatology 2010 diagnostic criteria, completed PROMs for function, quality of life and mood, alongside PDUS examination of 44 joints. Statistical analysis included logistic regression modelling and regularised (lasso) logistic regression methods.

resultsFrom 158 patients, 72 (46%) patients met FM criteria, with significantly worse tender joint counts and PROMs, but no differences in PDUS compared with the non-FM group. Categorising patients by PDUS+ joint presence and/or FM criteria, we identified four distinct groups: 43 (27.2%) patients with -FM-PD, 43 (27.2%) with -FM+PD, 42 (26.6%) with +FM-PD and 30 (19%) with +FM+PD. Both FM+ groups had worse PROMs for fatigue, mood and pain, compared with the FM- groups. We were unable to develop algorithms to identify different groups.

conclusionThe unexpected group -FM-PD group may have peripheral nociplastic pain, not commonly recognised in rheumatology. Only 46% of patients demonstrated PDUS+ inflammation. However clinical examination and PROMs did not reliably differentiate groups, emphasising PDUS remains an important tool.

Indexed as

Arthritis, RheumatoidFibromyalgiaCross-Sectional StudiesHumansInflammationPainQuality of LifeArthritis, RheumatoidFibromyalgiaPatient Reported Outcome Measures

Identifiers

PMID38508678
PMCPMC10953307

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.