Structural differences in adolescent brains can predict alcohol misuse

Author:

Rane Roshan Prakash1ORCID,de Man Evert Ferdinand2,Kim JiHoon3ORCID,Görgen Kai14ORCID,Tschorn Mira5,Rapp Michael A5,Banaschewski Tobias6,Bokde Arun LW7,Desrivieres Sylvane8,Flor Herta910,Grigis Antoine11,Garavan Hugh12,Gowland Penny A13,Brühl Rüdiger14ORCID,Martinot Jean-Luc15,Martinot Marie-Laure Paillere1516,Artiges Eric1517,Nees Frauke6918,Papadopoulos Orfanos Dimitri11ORCID,Lemaitre Herve1119,Paus Tomas2021,Poustka Luise22,Fröhner Juliane23,Robinson Lauren24,Smolka Michael N23ORCID,Winterer Jeanne13,Whelan Robert25,Schumann Gunter18,Walter Henrik1,Heinz Andreas1,Ritter Kerstin1,

Affiliation:

1. Charité – Universitätsmedizin Berlin (corporate member of Freie Universiät at Berlin, Humboldt-Universiät at zu Berlin, and Berlin Institute of Health), Department of Psychiatry and Psychotherapy, Bernstein Center for Computational Neuroscience

2. Faculty IV – Electrical Engineering and Computer Science, Technische Universität Berlin

3. Department of Education and Psychology, Freie Universität Berlin

4. Science of Intelligence, Research Cluster of Excellence

5. Social and Preventive Medicine, Department of Sports and Health Sciences, Intra-faculty unit “Cognitive Sciences”, Faculty of Human Science, and Faculty of Health Sciences Brandenburg, Research Area Services Research and e-Health, University of Potsdam

6. Department of Child and Adolescent Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University

7. Discipline of Psychiatry, School of Medicine and Trinity College Institute of Neuroscience, Trinity College Dublin

8. Centre for Population Neuroscience and Precision Medicine (PONS), Institute of Psychiatry, Psychology Neuroscience SGDP Centre, King’s College London

9. Institute of Cognitive and Clinical Neuroscience, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University

10. Department of Psychology, School of Social Sciences, University of Mannheim

11. NeuroSpin, CEA, Université Paris-Saclay

12. Departments of Psychiatry and Psychology, University of Vermont

13. Sir Peter Mansfield Imaging Centre School of Physics and Astronomy, University of Nottingham

14. Physikalisch-Technische Bundesanstalt

15. Institut National de la Santé et de la Recherche Médicale, INSERM U A10 ”Trajectoires développementales en psychiatrie” Universite Paris-Saclay, Ecole Normale Supérieure Paris-Saclay, CNRS, Centre Borelli

16. AP-HP Sorbonne Université, Department of Child and Adolescent Psychiatry, Pitié-Salpêtrière Hospital

17. Psychiatry Department, EPS Barthélémy Durand

18. PONS Research Group, Dept of Psychiatry and Psychotherapy, Campus Charite Mitte, Humboldt University

19. Institut des Maladies Neurodégénératives, UMR 5293, CNRS, CEA, University of Bordeaux

20. Department of Psychiatry, Faculty of Medicine and Centre Hospitalier Universitaire Sainte-Justine, University of Montreal

21. Departments of Psychiatry and Psychology, University of Toronto

22. Department of Child and Adolescent Psychiatry and Psychotherapy, University Medical Centre Göttingen

23. Department of Psychiatry and Neuroimaging Center, Technische Universität Dresden

24. Department of Psychological Medicine, Section for Eating Disorders, Institute of Psychiatry, Psychology and Neuroscience, King’s College London

25. School of Psychology and Global Brain Health Institute, Trinity College Dublin

Abstract

Alcohol misuse during adolescence (AAM) has been associated with disruptive development of adolescent brains. In this longitudinal machine learning (ML) study, we could predict AAM significantly from brain structure (T1-weighted imaging and DTI) with accuracies of 73 -78% in the IMAGEN dataset (n∼1182). Our results not only show that structural differences in brain can predict AAM, but also suggests that such differences might precede AAM behavior in the data. We predicted 10 phenotypes of AAM at age 22 using brain MRI features at ages 14, 19, and 22. Binge drinking was found to be the most predictable phenotype. The most informative brain features were located in the ventricular CSF, and in white matter tracts of the corpus callosum, internal capsule, and brain stem. In the cortex, they were spread across the occipital, frontal, and temporal lobes and in the cingulate cortex. We also experimented with four different ML models and several confound control techniques. Support Vector Machine (SVM) with rbf kernel and Gradient Boosting consistently performed better than the linear models, linear SVM and Logistic Regression. Our study also demonstrates how the choice of the predicted phenotype, ML model, and confound correction technique are all crucial decisions in an explorative ML study analyzing psychiatric disorders with small effect sizes such as AAM.

Funder

German Research Foundation

Research Foundation for International Scientists

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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