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Developmental pathways to amygdala-prefrontal function and internalizing symptoms in adolescence

Previous work demonstrates that early life stress (ELS) and HPA-axis function predict later psychopathology. Animal work and cross-sectional human studies suggest that this process might operate through amygdala-ventromedial prefrontal cortical (vmPFC) circuitry implicated in emotion regulation. The...

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Detalles Bibliográficos
Autores principales: Burghy, Cory A., Stodola, Diane E., Ruttle, Paula L., Molloy, Erin K., Armstrong, Jeffrey M., Oler, Jonathan A., Fox, Michelle E., Hayes, Andrea S., Kalin, Ned H., Essex, Marilyn J., Davidson, Richard J., Birn, Rasmus M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3509229/
https://www.ncbi.nlm.nih.gov/pubmed/23143517
http://dx.doi.org/10.1038/nn.3257
Descripción
Sumario:Previous work demonstrates that early life stress (ELS) and HPA-axis function predict later psychopathology. Animal work and cross-sectional human studies suggest that this process might operate through amygdala-ventromedial prefrontal cortical (vmPFC) circuitry implicated in emotion regulation. The current study prospectively investigated the roles of ELS and childhood basal cortisol in the development of adolescent resting-state functional connectivity (fcMRI) in the amygdala-PFC circuit. In females only, greater ELS predicted increased childhood cortisol levels, which, in turn, predicted decreased amygdala-vmPFC fcMRI 14 years later. Further, for females, amygdala-vmPFC fcMRI was inversely correlated with concurrent anxious symptoms, but positively associated with depressive symptoms, suggesting differing pathways from childhood cortisol function through adolescent amygdala-vmPFC functional connectivity to anxiety and depression. These data highlight that, for females, the effects of ELS and early HPA-axis function may be detected much later in the intrinsic processing of emotion-related brain circuits.