Chronotype, Longitudinal Volumetric Brain Variations Throughout Adolescence, and Depressive Symptom Development

计时型 心理学 舌回 邻苯二酚-O-甲基转移酶 纵向研究 前额叶皮质 精神科 昼夜节律 听力学 临床心理学 医学 认知 神经科学 等位基因 生物化学 病理 基因 化学
作者
Hélène Vulser,Hervé Lemaître,Stella Guldner,Pauline Bezivin-Frère,Martin Löffler,Anna S Sarvasmaa,J. Massicotte-Marquez,Éric Artiges,Marie‐Laure Paillère Martinot,Irina Filippi,Rubén Miranda,Argyris Stringaris,Betteke van Noort,Jani Penttilä,Yvonne Grimmer,Andreas Becker,Tobias Banaschewski,Arun L.W. Bokde,Sylvane Desrivières,Juliane H. Fröhner,Hugh Garavan,Antoine Grigis,Penny Gowland,Andreas Heinz,Dimitri Papadopoulos Orfanos,Luise Poustka,Michael N. Smolka,Philip A. Spechler,Henrik Walter,Robert Whelan,Günter Schumann,Herta Flor,Jean‐Luc Martinot,Frauke Nees
出处
期刊:Journal of the American Academy of Child and Adolescent Psychiatry [Elsevier]
卷期号:62 (1): 48-58 被引量:7
标识
DOI:10.1016/j.jaac.2022.06.003
摘要

Adolescence is a critical period for circadian rhythm, with a strong shift toward eveningness around age 14. Also, eveningness in adolescence has been found to predict later onset of depressive symptoms. However, no previous study has investigated structural variations associated with chronotype in early adolescence and how this adds to the development of depressive symptoms.Assessment of 128 community-based adolescents (51% girls) at age 14 and 19 years was performed. Using whole-brain voxel-based morphometry, baseline (at age 14) regional gray matter volumes (GMVs), follow-up (at age 19) regional GMVs, and longitudinal changes (between 14 and 19) associated with Morningness/Eveningness Scale in Children score and sleep habits at baseline were measured. The association of GMV with depressive symptoms at 19 years was studied, and the role of potential clinical and genetic factors as mediators and moderators was assessed.Higher eveningness was associated with larger GMV in the right medial prefrontal cortex at ages 14 and 19 in the whole sample. GMV in this region related to depressive symptoms at age 19 in catechol-O-methyltransferase (COMT) Val/Val, but not in Met COMT, carriers. Larger GMV also was observed in the right fusiform gyrus at age 14, which was explained by later wake-up time during weekends.In adolescence, eveningness and its related sleep habits correlated with distinct developmental patterns. Eveningness was specifically associated with GMV changes in the medial prefrontal cortex; this could serve as a brain vulnerability factor for later self-reported depressive symptoms in COMT Val/Val carriers.
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