Evidence map›Paper›PMID 30181555›Full record

ArticleTranslational psychiatry2018

Genetics of self-reported risk-taking behaviour, trans-ethnic consistency and relevance to brain gene expression.

Rona J Strawbridge, Joey Ward, Laura M Lyall, Elizabeth M Tunbridge, Breda Cullen, Nicholas Graham, Amy Ferguson, Keira J A Johnston, Donald M Lyall, Daniel Mackay and 11 more

Abstract read
In one paragraph

Article in Translational psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

16 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

21 authors.

Rona J StrawbridgeInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK. rona.strawbridge@glasgow.ac.uk.ORCID http://orcid.org/0000-0001-8506-3585
Joey WardInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
Laura M LyallInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
Elizabeth M TunbridgeDepartment of Psychiatry, University of Oxford, Oxford, UK.
Breda CullenInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.ORCID http://orcid.org/0000-0002-7259-9505
Nicholas GrahamInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
Amy FergusonInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
Keira J A JohnstonInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
Donald M LyallInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
Daniel MackayInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
Jonathan CavanaghInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
David M HowardDivision of Psychiatry, University of Edinburgh, Royal Edinburgh Hospital, Edinburgh, EH10 5HF, UK.ORCID http://orcid.org/0000-0002-6005-1972
Mark J AdamsDivision of Psychiatry, University of Edinburgh, Royal Edinburgh Hospital, Edinburgh, EH10 5HF, UK.ORCID http://orcid.org/0000-0002-3599-6018
Ian DearyDepartment of Psychology, University of Edinburgh, Edinburgh, EH8 9YL, UK.
Valentina Escott-PriceMRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.ORCID http://orcid.org/0000-0003-1784-5483
Michael O'DonovanMRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.ORCID http://orcid.org/0000-0001-7073-2379
Andrew M McIntoshDivision of Psychiatry, University of Edinburgh, Royal Edinburgh Hospital, Edinburgh, EH10 5HF, UK.ORCID http://orcid.org/0000-0002-0198-4588
Mark E S BaileySchool of Life Sciences, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.ORCID http://orcid.org/0000-0002-9788-2278
Jill P PellInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
Paul J HarrisonDepartment of Psychiatry, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-6719-1126
Daniel J SmithInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.ORCID http://orcid.org/0000-0002-2267-1951

Funding

British Heart FoundationDepartment of HealthMedical Research Council MC_PC_17228Medical Research Council MC_QA137853Medical Research Council MR/K026992/1Medical Research Council MR/K501335/1Medical Research Council MR/L010305/1Medical Research Council MR/L023784/2Medical Research Council MR/S003061/1Wellcome Trust
6 · The paper itself

Abstract

Risk-taking behaviour is an important component of several psychiatric disorders, including attention-deficit hyperactivity disorder, schizophrenia and bipolar disorder. Previously, two genetic loci have been associated with self-reported risk taking and significant genetic overlap with psychiatric disorders was identified within a subsample of UK Biobank. Using the white British participants of the full UK Biobank cohort (n = 83,677 risk takers versus 244,662 controls) for our primary analysis, we conducted a genome-wide association study of self-reported risk-taking behaviour. In secondary analyses, we assessed sex-specific effects, trans-ethnic heterogeneity and genetic overlap with psychiatric traits. We also investigated the impact of risk-taking-associated SNPs on both gene expression and structural brain imaging. We identified 10 independent loci for risk-taking behaviour, of which eight were novel and two replicated previous findings. In addition, we found two further sex-specific risk-taking loci. There were strong positive genetic correlations between risk-taking and attention-deficit hyperactivity disorder, bipolar disorder and schizophrenia. Index genetic variants demonstrated effects generally consistent with the discovery analysis in individuals of non-British White, South Asian, African-Caribbean or mixed ethnicity. Polygenic risk scores comprising alleles associated with increased risk taking were associated with lower white matter integrity. Genotype-specific expression pattern analyses highlighted DPYSL5, CGREF1 and C15orf59 as plausible candidate genes. Overall, our findings substantially advance our understanding of the biology of risk-taking behaviour, including the possibility of sex-specific contributions, and reveal consistency across ethnicities. We further highlight several putative novel candidate genes, which may mediate these genetic effects.

Indexed as

Genome-Wide Association StudyRisk-TakingAgedAttention Deficit Disorder with HyperactivityBiological Specimen BanksBipolar DisorderCalcium-Binding ProteinsFemaleGene ExpressionGenetic Predisposition to DiseaseHumansHydrolasesMagnetic Resonance ImagingMaleMicrotubule-Associated ProteinsMiddle AgedCalcium-Binding ProteinsCGREF1 protein, humanDPYSL5 protein, humanHydrolasesMicrotubule-Associated ProteinsNerve Tissue Proteins

Identifiers

PMID30181555
PMCPMC6123450

What OpenQuestion holds

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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.