BackgroundAdolescence is a transition period characterized by heightened emotional reactivity, which for some sets the stage for emerging depressive symptoms. Prior studies suggest that adolescent depression is associated with deviant cortical and subcortical brain structure. Longitudinal studies are, however, currently scarce, but critical to detect which adolescents are at risk for developing depressive symptoms.MethodsIn this longitudinal study, a community sample of 205 participants underwent magnetic resonance imaging (MRI) in three biennial waves (522 scans) spanning 5 years across ages 8–25 years. Depressive symptomatology was assessed using self‐report at the third time point. Mixed models were used to examine the relations between structural brain development, specifically regional change in cortical thickness, surface area and subcortical volumes (hippocampus and amygdala), and depressive symptoms.ResultsAccelerated frontal lobe cortical thinning was observed in adolescents who developed depressive symptoms at the third time point. This effect remained after controlling for parent‐reported affective problems at the first time point. Moreover, the effect was driven by specific lateral orbitofrontal and precentral regions. In addition, differential developmental trajectories of parietal cortical thickness and surface area in several regions were found for participants reporting higher depressive symptomatology, but these results did not survive correction for multiple comparisons. Volumes or developmental volume changes in hippocampus or amygdala were not related to depressive symptoms.ConclusionsThis study showed that emerging depression is associated with cortical thinning in frontal regions within individuals. These findings move beyond detecting cross‐sectional correlations and set the stage for early detection, which may inform future intervention.
HighlightsHippocampal subregions develop in differential ways from childhood to adulthood.Subiculum, CA1, ML and fimbria showed nonlinear trajectories with initial increases.Parasubiculum, presubiculum, CA2/3, CA4 and GC-DG showed linear volume decreases.There were no sex differences in hippocampal subregion development.General cognitive ability associated with CA2/3 and CA4 volumes and ML development.
Detailed descriptions of the development of the hippocampus promise to shed light on the neural foundation of development of memory and other cognitive functions, as well as the emergence of major mental disorders. Hippocampus is a heterogeneous structure with a well characterized internal complexity, but development of its distinct subregions in humans has remained poorly described. We analyzed magnetic resonance imaging (MRI) data from a large longitudinal sample (270 participants, 678 scans) using an automated segmentation tool and mixed models to delineate the development of hippocampal subregion volumes from childhood to adulthood. We also examined sex differences in subregion volumes and their development, and associations between hippocampal subregions and general cognitive ability. Nonlinear developmental trajectories with early volume increases were observed for subiculum, cornu ammonis (CA) 1, molecular layer (ML) and fimbria. In contrast, parasubiculum, presubiculum, CA2/3, CA4 and the granule cell layer of the dentate gyrus (GC-DG) showed linear volume decreases. No sex differences were found in hippocampal subregion development. Finally, general cognitive ability was positively associated with CA2/3 and CA4 volumes, as well as with ML development. In conclusion, hippocampal subregions appear to develop in diversified ways across adolescence, and specific subregions may link to general cognitive level.HighlightsHippocampal subregions develop in differential ways from childhood to adulthoodSubiculum, CA1, ML and fimbria showed nonlinear trajectories with initial increasesParasubiculum, presubiculum, CA2/3, CA4 and GC-DG showed linear volume decreasesThere were no sex differences in hippocampal subregion developmentGeneral cognitive ability associated with CA2/3 and CA4 volumes and ML development
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