Evidence map›Paper›PMID 25490859›Full record

ArticleBMC psychiatry2014

Chronic multisite pain in major depression and bipolar disorder: cross-sectional study of 149,611 participants in UK Biobank.

Barbara I Nicholl, Daniel Mackay, Breda Cullen, Daniel J Martin, Zia Ul-Haq, Frances S Mair, Jonathan Evans, Andrew M McIntosh, John Gallagher, Beverly Roberts and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 7% of its field
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

64 citing papers in PubMed, 2 syntheses or guidelines pooled it, 130 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Observational
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  8. Patterns of shared genetic risk between chronic pain, psychopathologies, and neuroticism.Clinical psychological science : a journal of the Association for Psychological Science · 2025
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  13. Pain in women with and without bipolar spectrum disorder.Frontiers in global women's health · 2025
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  14. Article
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  16. The pain and mental health comorbidity.Epidemiology and psychiatric sciences · 2024
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4 more citing papers are in PubMed but not listed here.

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

13 authors at 2 institutions in 1 country.

Barbara I NichollInstitute of Health & Wellbeing, University of Glasgow, Glasgow, Scotland, UK. Barbara.Nicholl@glasgow.ac.uk.
Daniel MackayInstitute of Health & Wellbeing, University of Glasgow, Glasgow, Scotland, UK. Daniel.Mackay@glasgow.ac.uk.
Breda CullenInstitute of Health & Wellbeing, University of Glasgow, Glasgow, Scotland, UK. Breda.Cullen@glasgow.ac.uk.
Daniel J MartinInstitute of Health & Wellbeing, University of Glasgow, Glasgow, Scotland, UK. Daniel.Martin@glasgow.ac.uk.
Zia Ul-HaqInstitute of Health & Wellbeing, University of Glasgow, Glasgow, Scotland, UK. z.ul-haq.2@research.gla.ac.uk.
Frances S MairInstitute of Health & Wellbeing, University of Glasgow, Glasgow, Scotland, UK. Frances.Mair@glasgow.ac.uk.
Jonathan EvansInstitute of Health & Wellbeing, University of Glasgow, Glasgow, Scotland, UK. Jonathan.Evans@glasgow.ac.uk.
Andrew M McIntoshDivision of Psychiatry, University of Edinburgh, Edinburgh, UK. andrew.mcintosh@ed.ac.uk.
John GallagherInstitute of Health & Wellbeing, University of Glasgow, Glasgow, Scotland, UK. Gallacher@cf.ac.uk.
Beverly RobertsCentre for Cognitive Ageing and Cognitive Epidemiology, Department of Psychology, University of Edinburgh, Edinburgh, UK. beverly.roberts@ed.ac.uk.
Ian J DearyCentre for Cognitive Ageing and Cognitive Epidemiology, Department of Psychology, University of Edinburgh, Edinburgh, UK. iand@staffmail.ed.ac.uk.
Jill P PellInstitute of Health & Wellbeing, University of Glasgow, Glasgow, Scotland, UK. Jill.Pell@glasgow.ac.uk.
Daniel J SmithInstitute of Health & Wellbeing, University of Glasgow, Glasgow, Scotland, UK. Daniel.Smith@glasgow.ac.uk.
University of Glasgow · GBUniversity of Edinburgh · GB

Funding

Medical Research Council G0700704Medical Research Council MC_QA137853Medical Research Council MR/K026992/1Wellcome Trust 093707Wellcome Trust 104036
6 · The paper itself

Abstract

backgroundChronic pain has a strong association with major depressive disorder (MDD), but there is a relative paucity of studies on the association between chronic multisite pain and bipolar disorder (BD). Such studies are required to help elucidate the complex biological and psychological overlap between pain and mood disorders. The aim of this study is to investigate the relationship between chronic multisite pain and mood disorder across the unipolar-bipolar spectrum.

methodsWe conducted a cross-sectional study of 149,611 UK Biobank participants. Self-reported depressive and bipolar features were used to categorise participants into MDD and BD groups and a non-mood disordered comparison group. Multinomial logistic regression was used to establish whether there was an association between extent of chronic pain (independent variable) and mood disorder category (dependent variable), using no pain as the referent category, and adjusting for a wide range of potential sociodemographic, lifestyle and comorbidity confounders.

resultsMultisite pain was significantly more prevalent in participants with BD and MDD, for example, 4-7 pain sites: BD 5.8%, MDD 4.5%, and comparison group 1.8% (p < 0.001). A relationship was observed between extent of chronic pain and risk of BD and persisted after adjusting for confounders (relative to individuals with no chronic pain): 2-3 sites RRR of BD 1.84 (95% CI 1.61, 2.11); 4-7 sites RRR of BD 2.39 (95% CI 1.88, 3.03) and widespread pain RRR of BD 2.37 (95% CI 1.73, 3.23). A similar relationship was observed between chronic pain and MDD: 2-3 sites RRR of MDD 1.59 (95% CI 1.54, 1.65); 4-7 sites RRR of MDD 2.13 (95% CI 1.98, 2.30); widespread pain RRR of MDD 1.86 (95% CI 1.66, 2.08).

conclusionsIndividuals who report chronic pain and multiple sites of pain are more likely to have MDD and are at higher risk of BD. These findings highlight an important aspect of comorbidity in MDD and BD and may have implications for understanding the shared neurobiology of chronic pain and mood disorders.

Indexed as

Biological Specimen BanksAdultAgedBipolar DisorderChronic PainCohort StudiesComorbidityCross-Sectional StudiesFemaleHumansMajor Depressive DisorderMaleMiddle AgedMood DisordersUnited Kingdom

Identifiers

PMID25490859
PMCPMC4297369
OpenAlexW1984330336

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.