Evidence map›Paper›PMID 26994398›Full record

ArticleSchizophrenia bulletin2016

Shared Etiology of Psychotic Experiences and Depressive Symptoms in Adolescence: A Longitudinal Twin Study.

Helena M S Zavos, Thalia C Eley, Philip McGuire, Robert Plomin, Alastair G Cardno, Daniel Freeman, Angelica Ronald

Open access · hybridAbstract readTwin Study
In one paragraph

Article in Schizophrenia bulletin, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.8field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  3. Research Review: A review of the past decade of family and genomic studies on adolescent mental health.Journal of child psychology and psychiatry, and allied disciplines · 2025
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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 at 5 institutions in 1 country.

Helena M S ZavosDepartment of Psychology, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK; a.ronald@bbk.ac.uk.
Thalia C EleyMedical Research Council, Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK;
Philip McGuireInstitute of Psychiatry, Psychology, and Neuroscience, King's College London, London, UK;
Robert PlominMedical Research Council, Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK;
Alastair G CardnoAcademic Unit of Psychiatry and Behavioural Sciences, University of Leeds, Leeds, UK;
Daniel FreemanDepartment of Psychiatry, University of Oxford, Oxford, UK;
Angelica RonaldCentre for Brain and Cognitive Development, Birkbeck, Department of Psychological Sciences, University of London, London, UK a.ronald@bbk.ac.uk.
King's College London · GBBirkbeck, University of London · GBMedical Research Council · GBUniversity of Leeds · GBUniversity of Oxford · GB

Funding

Department of Health RP-2014-05-003Medical Research Council G0500079Medical Research Council G0901245Medical Research Council G0902308Medical Research Council G1100559Medical Research Council G19/2Medical Research Council MR/M021475/1
6 · The paper itself

Abstract

Psychotic disorders and major depression, both typically adult-onset conditions, often co-occur. At younger ages psychotic experiences and depressive symptoms are often reported in the community. We used a genetically sensitive longitudinal design to investigate the relationship between psychotic experiences and depressive symptoms in adolescence. A representative community sample of twins from England and Wales was employed. Self-rated depressive symptoms, paranoia, hallucinations, cognitive disorganization, grandiosity, anhedonia, and parent-rated negative symptoms were collected when the twins were age 16 (N = 9618) and again on a representative subsample 9 months later (N = 2873). Direction and aetiology of associations were assessed using genetically informative cross-lagged models. Depressive symptoms were moderately correlated with paranoia, hallucinations, and cognitive disorganization. Lower correlations were observed between depression and anhedonia, and depression and parent-rated negative symptoms. Nonsignificant correlations were observed between depression and grandiosity. Largely the same genetic effects influenced depression and paranoia, depression and hallucinations, and depression and cognitive disorganization. Modest overlap in environmental influences also played a role in the associations. Significant bi-directional longitudinal associations were observed between depression and paranoia. Hallucinations and cognitive disorganization during adolescence were found to impact later depression, even after controlling for earlier levels of depression. Our study shows that psychotic experiences and depression, as traits in the community, have a high genetic overlap in mid-adolescence. Future research should test the prediction stemming from our longitudinal results, namely that reducing or ameliorating positive and cognitive psychotic experiences in adolescence would decrease later depressive symptoms.

Indexed as

HallucinationsMajor Depressive DisorderParanoid DisordersPsychotic DisordersAdolescentDiseases in TwinsFemaleHumansLongitudinal StudiesMaleadolescencedepressiongeneticspsychotic experiencestwin study

Identifiers

PMID26994398
PMCPMC4988737
OpenAlexW2289419266

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.