Interplay of early negative life events, development of orbitofrontal cortical thickness and depression in young adulthood

Author:

Backhausen Lea L.12ORCID,Granzow Jonas2,Fröhner Juliane H.1,Artiges Eric34,Paillère‐Martinot Marie‐Laure35,Lemaître Hervé6,Sticca Fabio7,Banaschewski Tobias8,Desrivières Sylvane9,Grigis Antoine6,Heinz Andreas10,Brühl Rüdiger11,Papadopoulos‐Orfanos Dimitri6,Poustka Luise12,Hohmann Sarah813,Robinson Lauren14,Walter Henrik10,Winterer Jeanne1015,Schumann Gunter91617,Martinot Jean‐Luc3,Smolka Michael N.1ORCID,Vetter Nora C.1218,

Affiliation:

1. Department of Psychiatry and Psychotherapy TUD Dresden University of Technology Dresden Germany

2. Department of Child and Adolescent Psychiatry Medical Faculty and University Hospital Carl Gustav Carus, TUD Dresden University of Technology Dresden Germany

3. Institut National de la Santé et de la Recherche Médicale INSERM U1299 “Trajectoires développementales en psychiatrie” Université Paris‐Saclay Ecole Normale supérieure Paris‐Saclay CNRS Centre Borelli Gif‐sur‐Yvette France

4. Department of Psychiatry Lab‐D‐Psy EPS Barthélémy Durand Etampes France

5. Department of Child and Adolescent Psychiatry Pitié‐Salpêtrière Hospital Paris France

6. NeuroSpin CEA Université Paris‐Saclay Gif‐sur‐Yvette France

7. Institute for Educational Support for Behaviour, Social‐Emotional, and Psychomotor Development University of Teacher Education in Special Needs Zurich Switzerland

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

9. Centre for Population Neuroscience and Precision Medicine (PONS) Institute of Psychiatry, Psychology & Neuroscience SGDP Centre King's College London London UK

10. Department of Psychiatry and Neurosciences Charité – Universitätsmedizin Berlin Corporate Member of Freie Universität Berlin Humboldt‐Universität zu Berlin, and Berlin Institute of Health Berlin Germany

11. Physikalisch‐Technische Bundesanstalt (PTB) Braunschweig and Berlin Berlin Germany

12. Department of Child and Adolescent Psychiatry and Psychotherapy University Medical Centre Göttingen Göttingen Germany

13. Department of Child and Adolescent Psychiatry Psychotherapy and Psychosomatics University Medical Center Hamburg Eppendorf Hamburg Germany

14. Department of Psychological Medicine Section for Eating Disorders Institute of Psychiatry, Psychology and Neuroscience King's College London London UK

15. Department of Education and Psychology Freie Universität Berlin Berlin Germany

16. Department of Psychiatry and Psychotherapy PONS Research Group Campus Charite Mitte Humboldt University Berlin and Leibniz Institute for Neurobiology Magdeburg Germany

17. Institute for Science and Technology of Brain‐inspired Intelligence (ISTBI) Fudan University Shanghai China

18. Department of Psychology MSB Medical School Berlin Berlin Germany

Abstract

AbstractBackgroundEarly negative life events (NLE) have long‐lasting influences on neurodevelopment and psychopathology. Reduced orbitofrontal cortex (OFC) thickness was frequently associated with NLE and depressive symptoms. OFC thinning might mediate the effect of NLE on depressive symptoms, although few longitudinal studies exist. Using a complete longitudinal design with four time points, we examined whether NLE during childhood and early adolescence predict depressive symptoms in young adulthood through accelerated OFC thinning across adolescence.MethodsWe acquired structural MRI from 321 participants at two sites across four time points from ages 14 to 22. We measured NLE with the Life Events Questionnaire at the first time point and depressive symptoms with the Center for Epidemiologic Studies Depression Scale at the fourth time point. Modeling latent growth curves, we tested whether OFC thinning mediates the effect of NLE on depressive symptoms.ResultsA higher burden of NLE, a thicker OFC at the age of 14, and an accelerated OFC thinning across adolescence predicted young adults' depressive symptoms. We did not identify an effect of NLE on OFC thickness nor OFC thickness mediating effects of NLE on depressive symptoms.ConclusionsUsing a complete longitudinal design with four waves, we show that NLE in childhood and early adolescence predict depressive symptoms in the long term. Results indicate that an accelerated OFC thinning may precede depressive symptoms. Assessment of early additionally to acute NLEs and neurodevelopment may be warranted in clinical settings to identify risk factors for depression.

Funder

Horizon 2020 Framework Programme

Fédération pour la Recherche sur le Cerveau

Bundesministerium für Bildung und Forschung

NIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer Research

Medical Research Council

Fondation pour la Recherche Médicale

Fondation de France

European Union Agency for Cybersecurity

Publisher

Wiley

Subject

General Medicine

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