Evidence map›Paper›PMID 39038862›Full record

ArticleBMJ open2024

Childhood neurodivergent traits, inflammation and chronic disabling fatigue in adolescence: a longitudinal case-control study.

Lisa Quadt, Jenny Csecs, Rod Bond, Neil A Harrison, Hugo D Critchley, Kevin A Davies, Jessica Eccles

Abstract read
In one paragraph

Article in BMJ open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

  1. Predictors of Somatic Symptom Severity in Adult Psychiatric Outpatients: A Cross-sectional Heart Rate Variability and Quantitative Electroencephalography Study.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2026
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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

7 authors.

Lisa QuadtDepartment of Clinical Neuroscience, Brighton and Sussex Medical School, Brighton, UK l.quadt@bsms.ac.uk.ORCID 0000-0002-5896-916X
Jenny CsecsBerkshire Healthcare NHS Foundation Trust, Bracknell, Bracknell Forest, UK.
Rod BondSchool of Psychology, University of Sussex, Brighton, UK.
Neil A HarrisonCardiff University Brain Research Imaging Centre, Cardiff University, Cardiff, UK.
Hugo D CritchleyDepartment of Clinical Neuroscience, Brighton and Sussex Medical School, Brighton, UK.
Kevin A DaviesDepartment of Clinical and Experimental Medicine, Brighton and Sussex Medical School, Brighton, UK.
Jessica EcclesDepartment of Clinical Neuroscience, Brighton and Sussex Medical School, Brighton, UK.ORCID 0000-0002-0062-1216

Funding

Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_PC_19009Wellcome Trust
6 · The paper itself

Abstract

objectivesTo test whether inflammatory processes link the expression of childhood neurodivergent traits to chronic disabling fatigue in adolescence.

designLongitudinal case-control study.

settingWe analysed data from The Avon Longitudinal Study of Parents and Children (ALSPAC).

participants8115 and 8036 children of the ALSPAC cohort at ages 7 and 9 years, respectively, 4563 of whom also completed self-report measures at age 18 years. PRIMARY AND SECONDARY OUTCOME MEASURES: We assessed if children scoring above screening threshold for autism/attention deficit hyperactivity disorder (ADHD) at ages 7 and 9 years had increased risk of chronic disabling fatigue at age 18 years, computing ORs and CIs for effects using binary logistic regression. Mediation analyses were conducted to test if an inflammatory marker (interleukin 6 (IL-6)) at age 9 years linked neurodivergent traits to chronic disabling fatigue at age 18 years.

resultsChildren with neurodivergent traits at ages 7 and 9 years were two times as likely to experience chronic disabling fatigue at age 18 years (likely ADHD OR=2.18 (95% CI=1.33 to 3.56); p=0.002; likely autism OR=1.78 (95% CI=1.17 to 2.72); p=0.004). Levels of IL-6 at age 9 were associated with chronic disabling fatigue at age 18 (OR=1.54 (95% CI=1.13 to 2.11); p=0.006). Inflammation at age 9 years mediated effects of neurodivergent traits on chronic disabling fatigue (indirect effect via IL-6: ADHD b=1.08 (95% CI=1.01 to 1.15); autism b=1.06; (95% CI=1.03 to 1.10)). All effects remained significant when controlling for the presence of depressive symptoms.

conclusionsOur results indicate higher risk of chronic disabling fatigue for children with neurodivergent traits, likely linked to higher levels of inflammation. The implementation of transdiagnostic screening criteria to inform support strategies to counteract risk early in life is recommended.

Indexed as

InflammationInterleukin-6AdolescentAttention Deficit Disorder with HyperactivityAutistic DisorderCase-Control StudiesChildFatigueFatigue Syndrome, ChronicFemaleHumansLogistic ModelsLongitudinal StudiesMaleInterleukin-6adolescentsdevelopmental neurology & neurodisabilityfatigue

Identifiers

PMID39038862
PMCPMC11733788

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