Evidence map›Paper›PMID 37787636›Full record

ArticleEarly intervention in psychiatry2024

Polygenic risk scores and the prediction of onset of mood and psychotic disorders in adolescents and young adults.

Jan Scott, Jacob J Crouse, Sarah Medland, Enda Byrne, Frank Iorfino, Brittany Mitchell, Nathan A Gillespie, Nicholas Martin, Naomi Wray, Ian B Hickie

Open access · bronzeAbstract readTwin Study
In one paragraph

Article in Early intervention in psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Article
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

10 authors at 4 institutions in 3 countries.

Jan ScottBrain and Mind Centre, The University of Sydney, Sydney, Australia.ORCID 0000-0002-7203-8601
Jacob J CrouseBrain and Mind Centre, The University of Sydney, Sydney, Australia.
Sarah MedlandQIMR Berghofer Institute of Medical Research, Brisbane, Australia.
Enda ByrneQIMR Berghofer Institute of Medical Research, Brisbane, Australia.
Frank IorfinoBrain and Mind Centre, The University of Sydney, Sydney, Australia.
Brittany MitchellQIMR Berghofer Institute of Medical Research, Brisbane, Australia.
Nathan A GillespieVirginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, Virginia, USA.
Nicholas MartinQIMR Berghofer Institute of Medical Research, Brisbane, Australia.
Naomi WrayInstitute of Molecular Bioscience, The University of Queensland, Brisbane, Australia.
Ian B HickieBrain and Mind Centre, The University of Sydney, Sydney, Australia.
The University of Sydney · AUQIMR Berghofer Medical Research Institute · AUThe University of Queensland · AUVirginia Commonwealth University · US

Funding

Genetic & environmental pathways to drug use, abuse & dependenceR00DA023549 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI GILLESPIE, NATHAN ALEXANDER · 2010 to 2012
$717k
Genetic & environmental pathways to drug use, abuse & dependenceK99DA023549 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI GILLESPIE, NATHAN ALEXANDER · 2008 to 2009
$166k
National Health and Medical Research Council, Australia 1031119National Health and Medical Research Council, Australia 1049911National Health and Medical Research Council, Australia APP10499110National Institute of Health, USA R00DA023549NIDA NIH HHS K99 DA023549NIDA NIH HHS R00 DA023549
6 · The paper itself

Abstract

aimTo examine whether polygenic risk scores (PRS) for neuroticism, depression, bipolar disorder and schizophrenia are higher in individuals manifesting trans-diagnostic risk factors for the development of major mental disorders and whether PRS enhance prediction of early onset full-threshold disorders.

methodsUsing data from the Brisbane Longitudinal Twin Study, we examined individual PRS for neuroticism, depression, bipolar disorder and schizophrenia, recorded evidence of subthreshold syndromes and family history of mood and/or psychotic disorders and noted progression to trans-diagnostic clinical caseness (onset of major mental disorders) at follow-up. We undertook multivariate, receiver operating curve and logistic regression analyses that were adjusted for known variables of influence (age, twin status, and so on).

resultsOf 1473 eligible participants (female = 866, 59%; mean age 26.3 years), 28% (n = 409) met caseness criteria for a mood and/or psychotic disorder. All PRS were higher in cases versus non-cases but associations with different levels of risk were inconsistent. The prediction of caseness (reported as area under the curve with 95% confidence intervals [CI]) improved from 0.68 (95% CI: 0.65, 0.71) when estimated using clinical risk factors alone up to 0.71 (95% CI: 0.69, 0.73) when PRS were added to the model. Logistic regression identified five variables that optimally classified individuals according to caseness: age, sex, individual risk characteristics, PRS for depression and mental health case status of cotwins or siblings.

conclusionsThe findings need replication. However, this exploratory study suggests that combining PRS with other risk factors has the potential to improve outcome prediction in youth.

Indexed as

Multifactorial InheritancePsychotic DisordersAdolescentAdultAge of OnsetBipolar DisorderFemaleGenetic Predisposition to DiseaseGenetic Risk ScoreHumansLongitudinal StudiesMaleMood DisordersNeuroticismRisk FactorsSchizophreniafamily historymental disordersonsetpolygenic risk scoresyouth

Identifiers

PMID37787636
PMCPMC11100301
OpenAlexW4387296202

What OpenQuestion holds

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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.