Evidence map›Paper›PMID 31851304›Full record

ArticleJAMA psychiatry2020

Association of Gray Matter and Personality Development With Increased Drunkenness Frequency During Adolescence.

Gabriel H Robert, Qiang Luo, Tao Yu, Congying Chu, Alex Ing, Tianye Jia, Dimitri Papadopoulos Orfanos, Erin Burke-Quinlan, Sylvane Desrivières, Barbara Ruggeri and 24 more

Open access · bronzeAbstract read
In one paragraph

Article in JAMA psychiatry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
8.7field-weighted citation impact, top 2% 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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it, 43 citations in OpenAlex.

  1. Pooled it
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  13. Alcohol and Cannabis Use and the Developing Brain.Alcohol research : current reviews · 2021
    Review
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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

34 authors at 17 institutions in 8 countries.

Gabriel H RobertInstitute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
Qiang LuoInstitute of Science and Technology for Brain-Inspired Intelligence, Fudan University, Shanghai, China.
Tao YuBio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Shanghai Jiao Tong University, Shanghai, China.
Congying ChuInstitute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
Alex IngInstitute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
Tianye JiaInstitute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
Dimitri Papadopoulos OrfanosDepartment of Systems Neuroscience, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Erin Burke-QuinlanInstitute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
Sylvane DesrivièresInstitute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
Barbara RuggeriInstitute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
Philip SpechlerDepartments of Psychiatry and Psychology, University of Vermont, Burlington.
Bader ChaaraniDepartments of Psychiatry and Psychology, University of Vermont, Burlington.
Nicole TayInstitute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
Tobias BanaschewskiDepartment of Child and Adolescent Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
Arun L W BokdeSchool of Medicine and Trinity College Institute of Neuroscience, Discipline of Psychiatry, Trinity College Dublin, Dublin, Ireland.
Uli BrombergDepartment of Systems Neuroscience, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Herta FlorDepartment of Cognitive and Clinical Neuroscience, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
Vincent FrouinDepartment of Systems Neuroscience, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Penny GowlandSir Peter Mansfield Imaging Centre School of Physics and Astronomy, University of Nottingham, University Park, Nottingham, United Kingdom.
Andreas HeinzDepartment of Psychiatry and Psychotherapy, Campus Charité Mitte, Charité, Universitätsmedizin Berlin, Berlin, Germany.
Bernd IttermannPhysikalisch-Technische Bundesanstalt, Braunschweig and Berlin, Berlin, Germany.
Jean-Luc MartinotInstitut National de la Santé et de la Recherche Médicale, INSERM Unit 1000 Neuroimaging & Psychiatry, Faculté de Médecine, Université Paris-Sud, Le Kremlin-Bicêtre, Sorbonne Paris Cité, Paris, France.
Marie-Laure Paillère MartinotInstitut National de la Santé et de la Recherche Médicale, INSERM Unit 1000 Neuroimaging & Psychiatry, Université Paris-Sud, University Paris Descartes-Sorbonne Paris Citél, Paris, France.
Frauke NeesDepartment of Psychology, School of Social Sciences, University of Mannheim, Mannheim, Germany.
Luise PoustkaDepartment of Child and Adolescent Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria.
Michael N SmolkaDepartment of Psychiatry and Neuroimaging Center, Technische Universität Dresden, Dresden, Germany.
Nora C VetterDepartment of Psychiatry and Neuroimaging Center, Technische Universität Dresden, Dresden, Germany.
Henrik WalterDepartment of Psychiatry and Psychotherapy, Campus Charité Mitte, Charité, Universitätsmedizin Berlin, Research Division of Mind and Brain Berlin, Berlin, Germany.
Robert WhelanDepartment of Psychology, University College Dublin, Belfield, Dublin, Ireland.
Patricia ConrodDepartment of Psychiatry and Addictology, Medical Faculty, University of Montreal, Montréal, Québec, Canada.
Ted BarkerInstitute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
Hugh GaravanDepartments of Psychiatry and Psychology, University of Vermont, Burlington.
Gunter SchumannInstitute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
IMAGEN Consortium
King's College London · GBUniversität Hamburg · DEUniversity of Vermont · USCharité - Universitätsmedizin Berlin · DETechnische Universität Dresden · DEUniversité Paris-Sud · FRUniversity of Mannheim · DEFudan University · CNHeidelberg University · DEInserm · FRMedical University of Vienna · ATPhysikalisch-Technische Bundesanstalt · DEShanghai Jiao Tong University · CNTrinity College Dublin · IEUniversité de Montréal · CAUniversity College Dublin · IEUniversity of Nottingham · GB

Funding

Training U54EB020403 · NIBIB · UNIVERSITY OF SOUTHERN CALIFORNIA · PI THOMPSON, PAUL M · 2014 to 2018
$10.1M
Axon, Testosterone and Mental Health during AdolescenceR01MH085772 · NIMH · BAYCREST CENTRE FOR GERIATRIC CARE · PI PAUS, TOMAS · 2010 to 2014
$1.5M
Medical Research Council MR/N000390/1Medical Research Council MR/N027558/1NIBIB NIH HHS U54 EB020403NIMH NIH HHS R01 MH085772
6 · The paper itself

Abstract

Importance: Alcohol abuse correlates with gray matter development in adolescents, but the directionality of this association remains unknown. Objective: To investigate the directionality of the association between gray matter development and increase in frequency of drunkenness among adolescents. Design, Setting, and Participants: This cohort study analyzed participants of IMAGEN, a multicenter brain imaging study of healthy adolescents in 8 European sites in Germany (Mannheim, Dresden, Berlin, and Hamburg), the United Kingdom (London and Nottingham), Ireland (Dublin), and France (Paris). Data from the second follow-up used in the present study were acquired from January 1, 2013, to December 31, 2016, and these data were analyzed from January 1, 2016, to March 31, 2018. Analyses were controlled for sex, site, socioeconomic status, family history of alcohol dependency, puberty score, negative life events, personality, cognition, and polygenic risk scores. Personality and frequency of drunkenness were assessed at age 14 years (baseline), 16 years (first follow-up), and 19 years (second follow-up). Structural brain imaging scans were acquired at baseline and second follow-up time points. Main Outcomes and Measures: Increases in drunkenness frequency were measured by latent growth modeling, a voxelwise hierarchical linear model was used to observe gray matter volume, and tensor-based morphometry was used for gray matter development. The hypotheses were formulated before the data analyses. Results: A total of 726 adolescents (mean [SD] age at baseline, 14.4 [0.38] years; 418 [58%] female) were included. The increase in drunkenness frequency was associated with accelerated gray matter atrophy in the left posterior temporal cortex (peak: t1,710 = -5.8; familywise error (FWE)-corrected P = 7.2 × 10-5; cluster: 6297 voxels; P = 2.7 × 10-5), right posterior temporal cortex (cluster: 2070 voxels; FWE-corrected P = .01), and left prefrontal cortex (peak: t1,710 = -5.2; FWE-corrected P = 2 × 10-3; cluster: 10 624 voxels; P = 1.9 × 10-7). According to causal bayesian network analyses, 73% of the networks showed directionality from gray matter development to drunkenness increase as confirmed by accelerated gray matter atrophy in late bingers compared with sober controls (n = 20 vs 60; β = 1.25; 95% CI, -2.15 to -0.46; t1,70 = 0.3; P = .004), the association of drunkenness increase with gray matter volume at age 14 years (β = 0.23; 95% CI, 0.01-0.46; t1,584 = 2; P = .04), the association between gray matter atrophy and alcohol drinking units (β = -0.0033; 95% CI, -6 × 10-3 to -5 × 10-4; t1,509 = -2.4; P = .02) and drunkenness frequency at age 23 years (β = -0.16; 95% CI, -0.28 to -0.03; t1,533 = -2.5; P = .01), and the linear exposure-response curve stratified by gray matter atrophy and not by increase in frequency of drunkenness. Conclusions and Relevance: This study found that gray matter development and impulsivity were associated with increased frequency of drunkenness by sex. These results suggest that neurotoxicity-related gray matter atrophy should be interpreted with caution.

Indexed as

Personality DevelopmentAdolescentAdolescent DevelopmentAlcoholic IntoxicationFemaleFrontal LobeGray MatterHumansImpulsive BehaviorMaleRisk FactorsSex FactorsTemporal LobeYoung Adult

Identifiers

PMID31851304
PMCPMC6990803
OpenAlexW2995530444

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.