The Neurobiological Effects and Intergenerational Transmission of Early Life Trauma on Children and Adolescents

A special issue of Children (ISSN 2227-9067). This special issue belongs to the section "Child Neurology".

Deadline for manuscript submissions: closed (31 July 2021) | Viewed by 2864

Special Issue Editor


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Guest Editor
Cumming School of Medicine, University of Calgary, 2500 University Dr. NW, Calgary AB T2N 1N4 , Canada
Interests: pediatric pain; neuroimaging; neurodevelopment; brain stimulation; mental health

Special Issue Information

Dear Colleagues,

The effects of early life trauma on multiple neurobiological processes such as genetics, epigenetics, cellular, immune, endocrine, brain and metabolic function, neurocircuitry, and neurochemistry is well-established in the literature. However, the consequences and co-morbidities of these neurobiological changes are still being realized. There is now converging evidence to support the theory that offspring are affected by previous generations’ exposure to trauma. Intergenerational risk is transferred not only through the genome, DNA methylation, and histone modification, but also through chemical exchanges in the womb during critical phases of brain development and parental modelling after birth. Considering the current COVID-19 pandemic, the global implications regarding the long-term effects of prenatal stress and trauma, and intergenerational transmission of trauma, are extremely topical. Understanding the neurobiological changes associated with exposures to trauma is necessary for developing individualized and targeted interventions to prevent the long-term repercussions of trauma in both the individual and their future progeny. Understanding and promoting factors that contribute to resilience will be important for interrupting intergenerational transmissions of trauma.

The goal of this Special Issue in Children is to highlight recent advances in trauma research examining the impact of early life traumatic experiences on children and adolescents. Reviews and/or original research articles may be focused on the basic sciences, clinical research, or both. Research involving neurobiological changes associated with early life trauma, comorbidities, intergenerational transmission, social transmission, interventions, and resiliency factors are welcomed. It is the hope that the articles submitted to this Special Issue will help to bring the field one step closer to finding solutions to the intergenerational impact of trauma.

I look forward to receiving your contributions.

Dr. Jillian Vinall Miller
Guest Editor

Manuscript Submission Information

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Keywords

  • trauma
  • posttraumatic stress symptoms
  • posttraumatic stress disorder
  • adverse early childhood experiences
  • neurobiology
  • brain
  • stress
  • neuroimaging
  • genetics
  • epigenetics
  • hormones
  • neurotransmitters
  • intergenerational transmission
  • parent
  • pregnancy
  • pandemic
  • COVID-19
  • coronavirus
  • child
  • adolescent
  • youth

Published Papers (1 paper)

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Research

14 pages, 280 KiB  
Article
Biomarkers of Allostatic Load as Correlates of Impairment in Youth with Chronic Pain: An Initial Investigation
by Sarah Nelson, Samantha Bento and Michelle Bosquet Enlow
Children 2021, 8(8), 709; https://0-doi-org.brum.beds.ac.uk/10.3390/children8080709 - 18 Aug 2021
Cited by 9 | Viewed by 2034
Abstract
Pediatric chronic pain is common and responsible for significant healthcare burden. However, the mechanisms underlying the development and/or maintenance of pediatric chronic pain remain poorly understood. Allostatic load (AL), or wear and tear on the nervous system following significant or prolonged stress, has [...] Read more.
Pediatric chronic pain is common and responsible for significant healthcare burden. However, the mechanisms underlying the development and/or maintenance of pediatric chronic pain remain poorly understood. Allostatic load (AL), or wear and tear on the nervous system following significant or prolonged stress, has been proposed to play a role in the maintenance of chronic pain, but minimal research has examined this possibility. This gap in research is particularly notable given the high exposure to adverse childhood experiences (ACEs; abuse/neglect, etc.) and psychological stress in this population. Accordingly, the current study aimed to preliminarily examine the measurement of AL in a treatment-seeking pediatric pain population. Biomarkers were collected during an already scheduled new patient pain evaluation and included salivary cortisol, dehydroepiandrosterone (DHEA), and C-reactive protein, in addition to waist–hip ratio, body-mass index, and blood pressure. A total of 61 children and adolescents with chronic pain (Mage = 14.47 years; 88.5% female and white/Caucasian) completed study procedures and were included in analyses. Preliminary results indicated that a multifactorial AL composite is feasible to assess for in a tertiary pain treatment setting and that over 50% of youth with chronic pain were classified as high risk for AL (two or more risk factors). Further, it was found that individual AL risk factors were significantly associated with functional disability and that AL may moderate the association between psychosocial and functional outcomes. Given the pilot nature of this study, results should be used to inform future investigations with larger and more diverse pediatric pain samples. Full article
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