Evidence map›Paper›PMID 35151465›Full record

ArticleBiological psychiatry2022

Persistent Childhood and Adolescent Anxiety and Risk for Psychosis: A Longitudinal Birth Cohort Study.

Isabel Morales-Muñoz, Edward R Palmer, Steven Marwaha, Pavan K Mallikarjun, Rachel Upthegrove

Open access · hybridAbstract read
In one paragraph

Article in Biological psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

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  3. Perceived connectedness during the perinatal period: Implications for parent and child well-being.Journal of family psychology : JFP : journal of the Division of Family Psychology of the American Psychological Association (Division 43) · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 2 countries.

Isabel Morales-MuñozInstitute for Mental Health, School of Psychology, University of Birmingham, Birmingham, United Kingdom; Department of Public Health Solutions, Finnish Institute for Health and Welfare, Helsinki, Finland. Electronic address: I.Morales-Munoz@bham.ac.uk.
Edward R PalmerInstitute for Mental Health, School of Psychology, University of Birmingham, Birmingham, United Kingdom; Birmingham and Solihull Mental Health Foundation Trust, Birmingham, United Kingdom.
Steven MarwahaInstitute for Mental Health, School of Psychology, University of Birmingham, Birmingham, United Kingdom; Specialist Mood Disorders Clinic, Zinnia Centre, Birmingham, United Kingdom; Barberry National Centre for Mental Health, Birmingham, United Kingdom.
Pavan K MallikarjunInstitute for Mental Health, School of Psychology, University of Birmingham, Birmingham, United Kingdom; Early Intervention Service, Birmingham Women's and Children's NHS Trust, Birmingham, United Kingdom.
Rachel UpthegroveInstitute for Mental Health, School of Psychology, University of Birmingham, Birmingham, United Kingdom; Early Intervention Service, Birmingham Women's and Children's NHS Trust, Birmingham, United Kingdom.
Birmingham Women’s and Children’s NHS Foundation Trust · GBBirmingham and Solihull Mental Health NHS Foundation Trust · GBCentre for Mental Health · GBFinnish Institute for Health and Welfare · FI

Funding

Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_PC_19009Medical Research Council MR/S037675/1Wellcome TrustWellcome Trust 217065/Z/19/Z
6 · The paper itself

Abstract

backgroundPersistent anxiety in childhood and adolescence could represent a novel treatment target for psychosis, potentially targeting activation of stress pathways and secondary nonresolving inflammatory response. Here, we examined the association between persistent anxiety through childhood and adolescence with individuals with psychotic experiences (PEs) or who met criteria for psychotic disorder (PD) at age 24 years. We also investigated whether C-reactive protein mediated any association.

methodsData from the Avon Longitudinal Study of Parents and Children (ALSPAC) were available in 8242 children at age 8 years, 7658 at age 10 years, 6906 at age 13 years, and 3889 at age 24 years. The Development and Well-Being Assessment was administered to capture child and adolescent anxiety. We created a composite score of generalized anxiety at ages 8, 10, and 13. PEs and PD were assessed at age 24, derived from the Psychosis-like Symptoms Interview. The mean of C-reactive protein at ages 9 and 15 years was used as a mediator.

resultsIndividuals with persistent high levels of anxiety were more likely to develop PEs (odds ratio 2.02, 95% CI 1.26-3.23, p = .003) and PD at age 24 (odds ratio 4.23, 95% CI 2.27-7.88, p < .001). The mean of C-reactive protein at ages 9 and 15 mediated the associations of persistent anxiety with PEs (bias-corrected estimate -0.001, p = .013) and PD (bias-corrected estimate 0.001, p = .003).

conclusionsPersistent high levels of anxiety through childhood and adolescence could be a risk factor for psychosis. Persistent anxiety is potentially related to subsequent psychosis via activation of stress hormones and nonresolving inflammation. These results contribute to the potential for preventive interventions in psychosis, with the novel target of early anxiety.

Indexed as

C-Reactive ProteinPsychotic DisordersAdolescentAdultAnxietyBirth CohortChildCohort StudiesHumansLongitudinal StudiesYoung AdultC-Reactive ProteinALSPACAnxietyC-reactive proteinInflammationPsychosisTrajectories

Identifiers

PMID35151465
PMCPMC9302897
OpenAlexW4200425664

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.