Early-life and pubertal stress differentially modulate grey matter development in human adolescents.
Anna TyborowskaInge VolmanHannah C M NiermannJ Loes PouwelsSanny SmeekensAntonius H N CillessenIvan ToniKarin RoelofsPublished in: Scientific reports (2018)
Animal and human studies have shown that both early-life traumatic events and ongoing stress episodes affect neurodevelopment, however, it remains unclear whether and how they modulate normative adolescent neuro-maturational trajectories. We characterized effects of early-life (age 0-5) and ongoing stressors (age 14-17) on longitudinal changes (age 14 to17) in grey matter volume (GMV) of healthy adolescents (n = 37). Timing and stressor type were related to differential GMV changes. More personal early-life stressful events were associated with larger developmental reductions in GMV over anterior prefrontal cortex, amygdala and other subcortical regions; whereas ongoing stress from the adolescents' social environment was related to smaller reductions over the orbitofrontal and anterior cingulate cortex. These findings suggest that early-life stress accelerates pubertal development, whereas an adverse adolescent social environment disturbs brain maturation with potential mental health implications: delayed anterior cingulate maturation was associated with more antisocial traits - a juvenile precursor of psychopathy.
Keyphrases
- early life
- mental health
- young adults
- functional connectivity
- prefrontal cortex
- white matter
- resting state
- endothelial cells
- physical activity
- stress induced
- healthcare
- induced pluripotent stem cells
- mental illness
- emergency department
- spinal cord injury
- childhood cancer
- climate change
- human health
- case control
- adverse drug