Evidence map›Paper›PMID 42253625›Full record

ArticleBrain, behavior, & immunity - health2026

Childhood and contemporaneous inflammation in depersonalisation and derealisation: Longitudinal evidence from the Avon Longitudinal Study of Parents and Children.

Evelyn Dilkes, Helge Gillmeister, Katie Daughters

Abstract read
In one paragraph

Article in Brain, behavior, & immunity - health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Evelyn DilkesInstitute of Social and Economic Research, University of Essex, Essex, UK.
Helge GillmeisterDepartment of Psychology, University of Essex, Essex, UK.
Katie DaughtersDepartment of Psychology, University of Essex, Essex, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Depersonalisation (DP) and derealisation (DR) are dissociative experiences that disrupt an individual's perception of themself and their environment. Recent evidence suggests a potential role for inflammatory processes. This study examined longitudinal associations between interleukin-6 (IL-6), C-reactive protein (CRP), and DP and DR across development. Methods: Data were drawn from the Avon Longitudinal Study of Parents and Children. IL-6 was measured at age 9 (n = 2606) and CRP at ages 9, 15, and 24 (n = 3323). DP and DR symptoms were assessed at ages 12, 17, and 24. Generalised linear mixed models examined associations between inflammatory markers and DP and DR using both early-life and time-varying approaches. Results: IL-6 at age 9 was not associated with DP or DR at any age. Higher CRP at age 9 was associated with increased odds of DR at age 12 but reduced odds of DR at ages 17 and 24. Higher CRP at age 9 was also associated with reduced odds of DP at age 24. Time-varying analyses differed: higher CRP at 24 was associated with reduced odds of DR at 24, but CRP measured in mid-adolescence was not associated with DR at 17, highlighting differences between fixed childhood and time-varying inflammatory models. Conclusions: Inflammatory processes may relate differently to DP and DR across development. Childhood CRP showed associations with later DP and DR, whereas contemporaneous CRP was associated only with DR, suggesting differing developmental patterns. These findings may reflect immune adaptation or cognitive mechanisms involved in the maintenance of symptoms.

Indexed as

AnxietyC-Reactive proteinDepersonalisationDerealisationDissociationInflammationInterleukin-6

Identifiers

PMID42253625
PMCPMC13235410

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