Evidence map›Paper›PMID 39875287›Full record

ArticleBritish journal of anaesthesia2025

The number of central nervous system-driven symptoms predicts subsequent chronic primary pain: evidence from UK Biobank.

Eoin Kelleher, Chelsea M Kaplan, Dorna Kheirabadi, Andrew Schrepf, Irene Tracey, Daniel J Clauw, Anushka Irani

Abstract read
In one paragraph

Article in British journal of anaesthesia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
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

7 authors.

Eoin KelleherNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK. Electronic address: Eoin.kelleher@ndcn.ox.ac.uk.
Chelsea M KaplanChronic Pain and Fatigue Research Center, University of Michigan, Ann Arbor, MI, USA.
Dorna KheirabadiChronic Pain and Fatigue Research Center, University of Michigan, Ann Arbor, MI, USA.
Andrew SchrepfChronic Pain and Fatigue Research Center, University of Michigan, Ann Arbor, MI, USA.
Irene TraceyNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Daniel J ClauwChronic Pain and Fatigue Research Center, University of Michigan, Ann Arbor, MI, USA.
Anushka IraniNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK; Department of Rheumatology, Mayo Clinic, Jacksonville, FL, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic primary pain describes conditions where pain is the principal problem rather than a consequence of another disease. Primary pain is thought to be primarily owing to nociplastic pain (i.e. pain as a result of altered nociception despite the absence of tissue damage). Primary pain is often accompanied by other bothersome central nervous system (CNS)-driven symptoms, including disturbed sleep, mood, and cognition; however, it is unclear whether these symptoms precede onset of primary pain.

methodsIn a prospective cohort study of the UK Biobank, we examined adults with no self-reported recent or chronic pain at baseline. Using linked primary care record data, we investigated the association between the number of CNS-driven symptoms and subsequent incidence of primary pain conditions. Multivariable regression analyses adjusted for sociodemographic and lifestyle factors.

resultsOf 502 369 participants, 70 630 (14.0%) met the inclusion criteria, with a mean (range) age of 56.7 (40-70) yr, 51% being female. After 7.4 (range 0.5-11.02) yr, 12.2% developed a primary pain condition. We observed a positive relationship between the number of CNS-driven symptoms at baseline and risk of future primary pain (HR 1.43, 95% CI 1.34-1.52, P<0.001). Participants with more CNS-driven symptoms at baseline were also more likely to have chronic and more severe nociplastic pain, but not non-nociplastic pain at follow-up.

conclusionsIn adults with no current self-reported pain, those with a greater number of CNS-driven symptoms at baseline were more likely to develop a primary pain condition. This suggests a potential opportunity for early intervention in mitigating the burden of primary pain.

Indexed as

Chronic PainAdultAgedBiological Specimen BanksCohort StudiesFemaleHumansMaleMiddle AgedProspective StudiesUK BiobankUnited Kingdomchronic painepidemiologymusculoskeletal painnociplastic painprimary pain

Identifiers

PMID39875287
PMCPMC11867065

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.