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Objective: Exposure to maltreatment in childhood increases risk for mental health difficulties across generations, affecting the development of offspring. In particular, maternal exposure to childhood maltreatment can shape the neurobiological development of offspring, especially in brain regions implicated in emotional health. However, relevant studies are cross-sectional, limiting understanding of how maternal childhood maltreatment might affect offspring neurodevelopment.
Method: Using data from the Growing Up in Singapore Towards healthy Outcomes (GUSTO) study, the authors investigated whether maternal report of childhood maltreatment was related to the development of offspring amygdala volume across 4 time points (ages 4.5-10.5 years; 1,143 scans from 430 children), how maltreatment-related alterations in amygdala volume development were related to anxiety symptoms in children at age 10.5 years (n = 267), and whether these associations differed by offspring sex.
Results: Greater maternal childhood maltreatment was associated with larger amygdala volume in girls at ages 4.5 to 10.5 years, which, in turn, was associated with lower levels of anxiety symptoms at age 10.5 years in girls, but not in boys. Maternal childhood maltreatment was not associated with the development of amygdala volume in boys.
Conclusion: These findings support the formulation that maternal childhood maltreatment has a sex-differentiated effect on brain development and mental health outcomes of offspring. These results advance understanding of the effects of maternal childhood maltreatment on children's brain development and risk for psychopathology.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12353134 | PMC |
http://dx.doi.org/10.1016/j.jaac.2025.03.027 | DOI Listing |
BJPsych Open
September 2025
Swansea University Medical School, Swansea University, UK.
Background: Pupils in alternative education provision, known as 'Educated in Other Than At School' (EOTAS) in Wales, UK, are among the most vulnerable learners and who, for reasons such as mental health or behavioural challenges, do not attend a mainstream or special school.
Aims: We compared self-harm, neurodevelopmental disorders and mental health conditions between EOTAS pupils and controls with similar characteristics, before and after being in EOTAS provision.
Method: This population-based electronic cohort study included pupils in Wales aged 7-18 years, from the academic years 2010-11 to 2018-19.
Biol Psychiatry
September 2025
Developmental Neuroscience and Neurogenetics Program, The Saban Research Institute, Los Angeles, CA; Child and Brain Development Program, Canadian Institute for Advanced Research, Toronto, Canada; Division of Endocrinology, Children's Hospital LA, Los Angeles, CA; Department of Pediatrics, Keck Scho
Background: Exposure to early life adversity (ELA), including childhood maltreatment, is one of the most significant risk factors for the emergence of psychosomatic disorders in adolescence and adulthood. Most investigations into biological processes that have been perturbed by ELA have profiled DNA methylation in whole blood and coalesced around perturbations of immunobiology being centrally insulted by ELA.
Methods: To identify novel molecular signatures that are enduringly perturbed by childhood maltreatment, we isolated circulating extracellular vesicles (EVs) from plasma collected from adolescent rhesus macaques that had either experienced nurturing maternal care (CONT, n = 7, 4M 3F) or maltreatment in infancy (MALT, n = 6, 3M 3F).
Front Psychiatry
August 2025
Neurobiology of Stress Research Group, Szentágothai Research Centre, University of Pécs, Pécs, Hungary.
Background: Previous studies indicate that hippocampal (subfield) and amygdala volumes may correlate with specific cognitive functions, coping strategies and emotion regulation. Here, we investigated associations between emotional processing and volumes of hippocampal subfields and amygdala. We focused on depressed patients since emotional dysregulation and hippocampal volume shrinkage are characteristic of them.
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September 2025
Center for Depression, Anxiety and Stress Research, McLean Hospital, Belmont, MA, USA.
Dysregulated dopaminergic signaling has been implicated in the pathophysiology of major depressive disorder (MDD) and childhood sexual abuse (CSA), but inconsistencies abound. In a multimodal PET-functional MRI study, harnessing the highly selective tracer [C]altropane, we investigated dopamine transporter availability (DAT) and resting-state functional connectivity (rsFC) within reward-related regions among 112 unmedicated individuals (MDD: n = 37, MDD/CSA: n = 18; CSA no MDD: n = 14; controls: n = 43). Striatal DAT and seed-based rsFC were assessed in the dorsal and ventral striatum and the ventral tegmental area.
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