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Association of Gray Matter and Personality Development With Increased Drunkenness Frequency During Adolescence.
Robert, Gabriel H; Luo, Qiang; Yu, Tao; Chu, Congying; Ing, Alex; Jia, Tianye; Papadopoulos Orfanos, Dimitri; Burke-Quinlan, Erin; Desrivières, Sylvane; Ruggeri, Barbara; Spechler, Philip; Chaarani, Bader; Tay, Nicole; Banaschewski, Tobias; Bokde, Arun L W; Bromberg, Uli; Flor, Herta; Frouin, Vincent; Gowland, Penny; Heinz, Andreas; Ittermann, Bernd; Martinot, Jean-Luc; Paillère Martinot, Marie-Laure; Nees, Frauke; Poustka, Luise; Smolka, Michael N; Vetter, Nora C; Walter, Henrik; Whelan, Robert; Conrod, Patricia; Barker, Ted; Garavan, Hugh; Schumann, Gunter.
Afiliação
  • Robert GH; Institute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
  • Luo Q; Behavior and Basal Ganglia Unit (EA-4712), University of Rennes 1, Rennes, France.
  • Yu T; Pôle Hospitalo-Universitaire de Psychiatrie Adulte, Rennes, France.
  • Chu C; Social, Genetic, and Developmental Psychiatry Centre, King's College London, London, United Kingdom.
  • Ing A; U1228, Empenn, Institut National de la Santé et de la Recherche Médicale & Institut National de Recherche en Informatique et Automatique, Paris, France.
  • Jia T; Institute of Science and Technology for Brain-Inspired Intelligence, Fudan University, Shanghai, China.
  • Papadopoulos Orfanos D; State Key Laboratory of Medical Neurobiology, MOE Frontiers Center for Brain Science, Institute of Brain Science, Fudan University, Shanghai, China.
  • Burke-Quinlan E; Key Laboratory of Computational Neuroscience and Brain-Inspired Intelligence, Fudan University, Ministry of Education, Shanghai, China.
  • Desrivières S; Bio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Shanghai Jiao Tong University, Shanghai, China.
  • Ruggeri B; Shanghai Center for Women and Children's Health, Shanghai, China.
  • Spechler P; Shanghai Key Laboratory of Psychotic Disorders, Shanghai Institute of Mental Health, Shanghai Jiao Tong University, Shanghai, China.
  • Chaarani B; Brain Science and Technology Research Center, Shanghai Jiao Tong University, Shanghai, China.
  • Tay N; Institute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
  • Banaschewski T; Social, Genetic, and Developmental Psychiatry Centre, King's College London, London, United Kingdom.
  • Bokde ALW; Institute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
  • Bromberg U; Social, Genetic, and Developmental Psychiatry Centre, King's College London, London, United Kingdom.
  • Flor H; Institute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
  • Frouin V; Social, Genetic, and Developmental Psychiatry Centre, King's College London, London, United Kingdom.
  • Gowland P; Department of Systems Neuroscience, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Heinz A; Institute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
  • Ittermann B; Social, Genetic, and Developmental Psychiatry Centre, King's College London, London, United Kingdom.
  • Martinot JL; Institute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
  • Paillère Martinot ML; Social, Genetic, and Developmental Psychiatry Centre, King's College London, London, United Kingdom.
  • Nees F; Institute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
  • Poustka L; Social, Genetic, and Developmental Psychiatry Centre, King's College London, London, United Kingdom.
  • Smolka MN; Departments of Psychiatry and Psychology, University of Vermont, Burlington.
  • Vetter NC; Departments of Psychiatry and Psychology, University of Vermont, Burlington.
  • Walter H; Institute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
  • Whelan R; Social, Genetic, and Developmental Psychiatry Centre, King's College London, London, United Kingdom.
  • Conrod P; Department of Child and Adolescent Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
  • Barker T; School of Medicine and Trinity College Institute of Neuroscience, Discipline of Psychiatry, Trinity College Dublin, Dublin, Ireland.
  • Garavan H; Department of Systems Neuroscience, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Schumann G; Department of Cognitive and Clinical Neuroscience, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
JAMA Psychiatry ; 77(4): 409-419, 2020 04 01.
Article em En | MEDLINE | ID: mdl-31851304
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; ß = 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 (ß = 0.23; 95% CI, 0.01-0.46; t1,584 = 2; P = .04), the association between gray matter atrophy and alcohol drinking units (ß = -0.0033; 95% CI, -6 × 10-3 to -5 × 10-4; t1,509 = -2.4; P = .02) and drunkenness frequency at age 23 years (ß = -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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Desenvolvimento da Personalidade / Intoxicação Alcoólica / Substância Cinzenta Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Desenvolvimento da Personalidade / Intoxicação Alcoólica / Substância Cinzenta Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article