Evidence map›Paper›PMID 37353490›Full record

ArticleTranslational psychiatry2023

Developmental manifestations of polygenic risk for bipolar disorder from infancy to middle childhood.

Ragna Bugge Askeland, Laurie J Hannigan, Kevin S O'Connell, Elizabeth C Corfield, Oleksandr Frei, Anita Thapar, George Davey Smith, Ted Reichborn-Kjennerud, Ole A Andreassen, Helga Ask and 1 more

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
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

11 authors at 4 institutions in 2 countries.

Ragna Bugge AskelandDepartment of Mental Disorders, Norwegian Institute of Public Health, 0473, Oslo, Norway. ragnabugge.askeland@fhi.no.ORCID 0000-0002-7465-0634
Laurie J HanniganDepartment of Mental Disorders, Norwegian Institute of Public Health, 0473, Oslo, Norway.ORCID 0000-0003-3123-5411
Kevin S O'ConnellNORMENT Centre, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Elizabeth C CorfieldDepartment of Mental Disorders, Norwegian Institute of Public Health, 0473, Oslo, Norway.ORCID 0000-0002-0119-157X
Oleksandr FreiNORMENT Centre, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Anita ThaparDivision of Psychological Medicine and Clinical Neurosciences; Centre for Neuropsychiatric Genetics and Genomics; Wolfson Centre for Young People's Mental Health, Cardiff University School of Medicine, Cardiff, Wales, UK.ORCID 0000-0002-3689-737X
George Davey SmithMedical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.ORCID 0000-0002-1407-8314
Ted Reichborn-KjennerudDepartment of Mental Disorders, Norwegian Institute of Public Health, 0473, Oslo, Norway.ORCID 0000-0003-4653-0034
Ole A AndreassenNORMENT Centre, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0002-4461-3568
Helga Ask *Department of Mental Disorders, Norwegian Institute of Public Health, 0473, Oslo, Norway.ORCID 0000-0003-0149-5319
Alexandra Havdahl *Department of Mental Disorders, Norwegian Institute of Public Health, 0473, Oslo, Norway.
Norwegian Institute of Public Health · NOOslo University Hospital · NOCardiff University · GBUniversity of Bristol · GB

Funding

Medical Research Council MC_UU_00032/1Medical Research Council MR/L010305/1
6 · The paper itself

Abstract

Knowledge on how genetic risk for bipolar disorder manifests in developmental, emotional or behavioral traits during childhood is lacking. This issue is important to address to inform early detection and intervention efforts. We investigated whether polygenic risk for bipolar disorder is associated with developmental outcomes during early to middle childhood in the general population, and if associations differ between boys and girls. Our sample consisted of 28 001 children from the Norwegian Mother, Father and Child Cohort study, a prospective pregnancy cohort with available genotype and developmental data. Mothers reported on a range of developmental outcomes in their children at 6 and 18 months, 3, 5 and 8 years. Polygenic risk scores reflecting common variant liability to bipolar disorder were calculated. Linear regression models were used in a multi-group framework to investigate associations between polygenic risk score and developmental outcomes, using sex as a grouping variable. We found robust evidence for an association between polygenic risk scores for bipolar disorder and conduct difficulties (β = 0.041, CI = 0.020-0.062) and oppositional defiant difficulties (β = 0.032, CI = 0.014-0.051) at 8 years. Associations with most other outcomes were estimated within the region of practical equivalence to zero (equivalence range D = -0.1 to 0.1), with the exceptions of negative association for activity levels (β = -0.028, CI = -0.047- -0.010) at age 5 and benevolence (β = -0.025, CI = -0.043 to -0.008) at age 8, and positive association for motor difficulties (β = 0.025, CI = 0.008-0.043) at age 3, inattention (β = 0.021, CI = 0.003-0.041) and hyperactivity (β = 0.025, CI = 0.006-0.044) at age 8. Our results suggest that genetic risk for bipolar disorder manifests as disruptive behaviors like oppositional defiant and conduct difficulties in childhood in the general population.

Indexed as

Attention Deficit Disorder with HyperactivityBipolar DisorderChildChild, PreschoolCohort StudiesEmotionsFemaleHumansInfantMaleMothersProspective Studies

Identifiers

PMID37353490
PMCPMC10290060
OpenAlexW4381798517

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.