Evidence map›Paper›PMID 36277463›Full record

ArticleBrain, behavior, & immunity - health2022

Early-life inflammatory markers and subsequent psychotic and depressive episodes between 10 to 28 years of age.

Amelia J Edmondson-Stait, Xueyi Shen, Mark J Adams, Miruna C Barbu, Hannah J Jones, Veronique E Miron, Judith Allardyce, James P Boardman, Stephen M Lawrie, Andrew M McIntosh and 3 more

Open access · goldAbstract read
In one paragraph

Article in Brain, behavior, & immunity - health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 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

13 authors at 4 institutions in 1 country.

Amelia J Edmondson-StaitTranslational Neuroscience PhD Programme, Centre for Clinical Brain Sciences, University of Edinburgh, UK.
Xueyi ShenCentre for Clinical Brain Sciences, University of Edinburgh, UK.
Mark J AdamsCentre for Clinical Brain Sciences, University of Edinburgh, UK.
Miruna C BarbuCentre for Clinical Brain Sciences, University of Edinburgh, UK.
Hannah J JonesNational Institute for Health Research Bristol Biomedical Research Centre, At University Hospitals Bristol and Weston NHS Foundation Trust and the University of Bristol, UK.
Veronique E MironMedical Research Council Centre for Reproductive Health, The Queen's Medical Research Institute, The University of Edinburgh, UK.
Judith AllardyceCentre for Clinical Brain Sciences, University of Edinburgh, UK.
James P BoardmanCentre for Clinical Brain Sciences, University of Edinburgh, UK.
Stephen M LawrieCentre for Clinical Brain Sciences, University of Edinburgh, UK.
Andrew M McIntoshCentre for Clinical Brain Sciences, University of Edinburgh, UK.
Golam M KhandakerMRC Integrative Epidemiology Unit, Population Health Sciences, Bristol Medical School, University of Bristol, UK.
Alex S F KwongCentre for Clinical Brain Sciences, University of Edinburgh, UK.
Heather C WhalleyCentre for Clinical Brain Sciences, University of Edinburgh, UK.
University of Edinburgh · GBMRC Centre for Reproductive Health · GBUniversity Hospitals Bristol NHS Foundation Trust · GBUniversity of Bristol · GB

Funding

Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_PC_17213Medical Research Council MC_PC_19009Medical Research Council MR/L010305/1Medical Research Council MR/M006727/1Medical Research Council MR/M020827/1Medical Research Council MR/S037675/1Medical Research Council MR/V004905/1Medical Research Council MR/V031260/1Medical Research Council MR/W014416/1Wellcome Trust 209176/Z/17/Z
6 · The paper itself

Abstract

Inflammation is implicated in depression and psychosis, including association of childhood inflammatory markers on the subsequent risk of developing symptoms. However, it is unknown whether early-life inflammatory markers are associated with the number of depressive and psychotic symptoms from childhood to adulthood. Using the prospective Avon Longitudinal Study of Children and Parents birth cohort (N = up-to 6401), we have examined longitudinal associations of early-life inflammation [exposures: interleukin-6 (IL-6), C-reactive protein (CRP) levels at age 9y; IL-6 and CRP DNA-methylation (DNAm) scores at birth and age 7y; and IL-6 and CRP polygenic risk scores (PRSs)] with the number of depressive episodes and psychotic experiences (PEs) between ages 10-28 years. Psychiatric outcomes were assessed using the Short Mood and Feelings Questionnaire and Psychotic Like Symptoms Questionnaires, respectively. Exposure-outcome associations were tested using negative binomial models, which were adjusted for metabolic and sociodemographic factors. Serum IL-6 levels at age 9y were associated with the total number of depressive episodes between 10 and 28y in the base model (n = 4835; β = 0.066; 95%CI:0.020-0.113; pFDR = 0.041) which was weaker when adjusting for metabolic and sociodemographic factors. Weak associations were observed between inflammatory markers (serum IL-6 and CRP DNAm scores) and total number of PEs. Other inflammatory markers were not associated with depression or PEs. Early-life inflammatory markers are associated with the burden of depressive episodes and of PEs subsequently from childhood to adulthood. These findings support a potential role of early-life inflammation in the aetiology of depression and psychosis and highlight inflammation as a potential target for treatment and prevention.

Indexed as

ALSPACDepressionInflammationLife courseOmicsPsychotic experiences

Identifiers

PMID36277463
PMCPMC9582583
OpenAlexW4304091938

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.