Evidence map›Paper›PMID 27476619›Full record

ArticlePsychological medicine2017

Childhood interleukin-6, C-reactive protein and atopic disorders as risk factors for hypomanic symptoms in young adulthood: a longitudinal birth cohort study.

J F Hayes, G M Khandaker, J Anderson, D Mackay, S Zammit, G Lewis, D J Smith, D P J Osborn

Open access · hybridAbstract read
In one paragraph

Article in Psychological medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 37 citations in OpenAlex.

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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 at 4 institutions in 2 countries.

J F HayesDivision of Psychiatry,UCL,London,UK.
G M KhandakerDepartment of Psychiatry,University of Cambridge,Cambridge,UK.
J AndersonInstitute of Health and Wellbeing,University of Glasgow,Glasgow,UK.
D MackayInstitute of Health and Wellbeing,University of Glasgow,Glasgow,UK.
S ZammitInstitute of Psychological Medicine and Clinical Neurosciences,Cardiff University School of Medicine,Cardiff,UK.
G LewisDivision of Psychiatry,UCL,London,UK.
D J SmithInstitute of Health and Wellbeing,University of Glasgow,Glasgow,UK.
D P J OsbornDivision of Psychiatry,UCL,London,UK.
University College Lahore · PKUniversity of Glasgow · GBUniversity of Bristol · GBUniversity of Cambridge · GB

Funding

Medical Research Council G0801418Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MR/K021362/1Wellcome TrustWellcome Trust 102215/2/13/2
6 · The paper itself

Abstract

backgroundThere are no existing longitudinal studies of inflammatory markers and atopic disorders in childhood and risk of hypomanic symptoms in adulthood. This study examined if childhood: (1) serum interleukin-6 (IL-6) and C-reactive protein (CRP); and (2) asthma and/or eczema are associated with features of hypomania in young adulthood.

methodParticipants in the Avon Longitudinal Study of Parents and Children, a prospective general population UK birth cohort, had non-fasting blood samples for IL-6 and CRP measurement at the age of 9 years (n = 4645), and parents answered a question about doctor-diagnosed atopic illness before the age of 10 years (n = 7809). These participants completed the Hypomania Checklist at age 22 years (n = 3361).

resultsAfter adjusting for age, sex, ethnicity, socio-economic status, past psychological and behavioural problems, body mass index and maternal postnatal depression, participants in the top third of IL-6 values at 9 years, compared with the bottom third, had an increased risk of hypomanic symptoms by age 22 years [adjusted odds ratio 1.77, 95% confidence interval (CI) 1.10-2.85, p < 0.001]. Higher IL-6 levels in childhood were associated with adult hypomania features in a dose-response fashion. After further adjustment for depression at the age of 18 years this association remained (adjusted odds ratio 1.70, 95% CI 1.03-2.81, p = 0.038). There was no evidence of an association of hypomanic symptoms with CRP levels, asthma or eczema in childhood.

conclusionsHigher levels of systemic inflammatory marker IL-6 in childhood were associated with hypomanic symptoms in young adulthood, suggesting that inflammation may play a role in the pathophysiology of mania. Inflammatory pathways may be suitable targets for the prevention and intervention for bipolar disorder.

Indexed as

AsthmaC-Reactive ProteinEczemaAdolescentAdultBipolar DisorderChildHumansInterleukin-6Longitudinal StudiesRisk FactorsUnited KingdomYoung AdultC-Reactive ProteinIL6 protein, humanInterleukin-6Atopic disorderscohort studieshypomaniainflammation

Identifiers

PMID27476619
PMCPMC5197925
OpenAlexW2504888768

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LicenceCC BY
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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.