TY - JOUR
T1 - Neurobiology of early life adversity
T2 - A systematic review of meta-analyses towards an integrative account of its neurobiological trajectories to mental disorders
AU - Hakamata, Yuko
AU - Suzuki, Yuhki
AU - Kobashikawa, Hajime
AU - Hori, Hiroaki
N1 - Publisher Copyright:
© 2022 The Author(s)
PY - 2022/4
Y1 - 2022/4
N2 - Adverse childhood experiences (ACEs) may leave long-lasting neurobiological scars, increasing the risk of developing mental disorders in later life. However, no review has comprehensively integrated existing evidence across the fields: hypothalamic–pituitary–adrenal axis, immune/inflammatory system, neuroimaging, and genetics/epigenetics. We thus systematically reviewed previous meta-analyses towards an integrative account of ACE-related neurobiological alterations. Following Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guideline, a total of 27 meta-analyses until October 2021 were identified. This review found that individuals with ACEs possess blunted cortisol response to psychosocial stressors, low-grade inflammation evinced by increased C-reactive protein levels, exaggerated amygdalar response to emotionally negative information, and diminished hippocampal gray matter volume. Importantly, these alterations were consistently observed in those with and without psychiatric diagnosis. These findings were integrated and discussed in a schematic model of ACE-related neurobiological alterations. Future longitudinal research based on multidisciplinary approach is imperative for ACE-related mental disorders’ prevention and treatment.
AB - Adverse childhood experiences (ACEs) may leave long-lasting neurobiological scars, increasing the risk of developing mental disorders in later life. However, no review has comprehensively integrated existing evidence across the fields: hypothalamic–pituitary–adrenal axis, immune/inflammatory system, neuroimaging, and genetics/epigenetics. We thus systematically reviewed previous meta-analyses towards an integrative account of ACE-related neurobiological alterations. Following Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guideline, a total of 27 meta-analyses until October 2021 were identified. This review found that individuals with ACEs possess blunted cortisol response to psychosocial stressors, low-grade inflammation evinced by increased C-reactive protein levels, exaggerated amygdalar response to emotionally negative information, and diminished hippocampal gray matter volume. Importantly, these alterations were consistently observed in those with and without psychiatric diagnosis. These findings were integrated and discussed in a schematic model of ACE-related neurobiological alterations. Future longitudinal research based on multidisciplinary approach is imperative for ACE-related mental disorders’ prevention and treatment.
KW - Childhood maltreatment
KW - Childhood trauma
KW - Connectivity
KW - DNA methylation
KW - Dorsolateral prefrontal cortex
KW - Gene
KW - Glucocorticoid
KW - Interleukin
KW - Norepinephrine
KW - White matter integrity
UR - http://www.scopus.com/inward/record.url?scp=85129332878&partnerID=8YFLogxK
U2 - 10.1016/j.yfrne.2022.100994
DO - 10.1016/j.yfrne.2022.100994
M3 - 総説
C2 - 35331780
AN - SCOPUS:85129332878
SN - 0091-3022
VL - 65
JO - Frontiers in Neuroendocrinology
JF - Frontiers in Neuroendocrinology
M1 - 100994
ER -