Biological embedding of childhood adversity: from physiological mechanisms to clinical implications

Anne E Berens1,2,3, Sarah K G Jensen1,2,3, Charles A Nelson4,5,6,7

  • 1Boston Children's Hospital, Boston, Massachusetts, USA.

BMC Medicine
|July 21, 2017
PubMed

Insights

Early life adversity biologically embeds, increasing risks for chronic diseases like diabetes and heart disease. Understanding molecular mechanisms is key to developing interventions for better public health outcomes.

Area of Science:

  • Psychoneuroimmunology
  • Developmental Origins of Health and Disease (DOHaD)
  • Molecular Epidemiology

Background:

  • Adverse psychosocial exposures in early life (e.g., child maltreatment, caregiver stress, violence) are linked to increased lifetime risk of chronic diseases.
  • Epidemiological studies show associations between early adversity and conditions such as diabetes, heart disease, cancers, and psychiatric illnesses.
  • Emerging research explores molecular mechanisms through which early adversity impacts physiology across body systems.

Purpose of the Study:

  • To review the evidence on molecular mechanisms linking early life adversity to long-term health outcomes.
  • To highlight the biological embedding of early adversity in physiological alterations.
  • To call for action from researchers, clinicians, policymakers, and practitioners.

Main Methods:

  • Literature review of epidemiological and molecular studies.
  • Synthesis of evidence on biological pathways affected by early adversity.
  • Identification of implications for public health and clinical practice.

Main Results:

  • Childhood psychosocial adversity profoundly affects neural, endocrine, immune, and metabolic physiology.
  • Key molecular mechanisms include disrupted neural networks, neuroendocrine stress dysregulation, and chronic inflammation.
  • These physiological disruptions increase susceptibility to common diseases throughout the lifespan.

Conclusions:

  • Evidence has significant implications for clinical practice, biomedical research, and public health policy.
  • Recommendations include increased screening for early life exposures in children and adults.
  • Urgent need for scaling up interventions, policy advocacy, and continued research for evidence-based strategies.
Abstract

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