bioRxivNeurosciencePreprint
Early life stress alters lifespan trajectories of amygdala development: a cross-species model of amygdala burnout
Megan SheppardiD, Jalil Rasgado‐ToledoiD, Luis A. Trujillo-VillarrealiD, Marta Czime LitwińczukiD, Katie L. MoraniD, Elizabeth McManusiD, Rebecca ElliottiD, Niall W. DuncaniD, Eduardo A. Garza‐VillarrealiD, Tobias BanaschewskiiD, Gareth J. BarkeriD, Arun L.W. BokdeiD, Rüdiger BrühliD, Sylvane DesrivièresiD, Herta FloriD, Antoine GrigisiD, Andreas HeinziD, Frauke NeesiD, Dimitri Papadopoulos OrfanosiD, Luise PoustkaiD, Michael N. SmolkaiD, Nathalie E. HolziD, Nilakshi VaidyaiD, Henrik WalteriD, Robert WhelaniD, , Nils MuhlertiD
Abstract
Early-life stress is associated with alterations in amygdala volume, but findings vary across studies and species. Rodent models typically report increased amygdala volume, whereas human studies often find reductions or mixed effects. We propose the amygdala burnout hypothesis, which suggests that early-life stress alters amygdala developmental trajectories, producing initial volumetric increases that are followed by reductions later in life. To test this hypothesis, we examined amygdala development across rodent and human cohorts spanning adolescence to older adulthood. In rodents, chronic stress was associated with increased amygdala nuclei volumes during adolescence. Comparable increases were observed in adolescents from the IMAGEN consortium, with evidence of a dose-dependent association between childhood stress and amygdala developmental trajectories. In contrast, analyses of older adults from the UK Biobank revealed reduced bilateral amygdala volume associated with early-life stress. Together, these findings support a developmental model that reconciles previously conflicting observations across species and age groups. Early-life stress is associated with alterations in amygdala volume, but findings vary across studies and species. Rodent models typically report increased amygdala volume, whereas human studies often find reductions or mixed effects. We propose the amygdala burnout hypothesis, which suggests that early-life stress alters amygdala developmental trajectories, producing initial volumetric increases that are followed by reductions later in life. To test this hypothesis, we examined amygdala development across rodent and human cohorts spanning adolescence to older adulthood. In rodents, chronic stress was associated with increased amygdala nuclei volumes during adolescence. Comparable increases were observed in adolescents from the IMAGEN consortium, with evidence of a dose-dependent association between childhood stress and amygdala developmental trajectories. In contrast, analyses of older adults from the UK Biobank revealed reduced bilateral amygdala volume associated with early-life stress. Together, these findings support a developmental model that reconciles previously conflicting observations across species and age groups.
- organism: mouse
- organism: human
- assay: imaging
- research focus: cell type annotation
- research focus: spatial domain detection
- research focus: differential expression
- research focus: trajectory inference
- approach: statistical model
- Citations
- 0
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