A biomarker of brain arousal mediates the intergenerational link between maternal and child post-traumatic stress

Marie-Pierre Deiber1, Virginie C Pointet Perizzolo2, Dominik A Moser3

  • 1Department of Psychiatry, University of Geneva, Geneva, Switzerland; Department of Psychiatry, University Hospitals of Geneva, Geneva, Switzerland.

PubMed

Insights

Maternal posttraumatic stress disorder (PTSD) linked to child PTSD symptoms may stem from altered brain activity. Children of mothers with PTSD show reduced power-law exponent (PLE), indicating hyper-arousal, which mediates the intergenerational risk. This suggests potential neurofeedback therapies for affected families.

Area of Science:

  • Neuroscience
  • Child Psychology
  • Psychiatry

Background:

  • Intergenerational transmission of trauma is a significant concern.
  • Maternal interpersonal violence-related posttraumatic stress disorder (IPV-PTSD) impacts child emotional regulation and mental health risk.
  • Potential EEG biomarkers mediating maternal IPV-PTSD effects on child mental health, particularly PTSD risk, were unexplored.

Purpose of the Study:

  • To investigate resting brain activity biomarkers in children of mothers with and without IPV-PTSD.
  • To examine if the aperiodic exponent of the power spectrum (PLE) mediates the link between maternal IPV-PTSD severity and child PTSD symptoms.
  • To explore the intergenerational impact of maternal IPV-PTSD on child neurobehavioral development.

Main Methods:

  • High-density EEG recordings of resting brain activity in 57 children (34 from mothers with IPV-PTSD, 23 from controls).
  • Analysis of alpha band spectral power and the aperiodic exponent of the power spectrum (PLE).
  • Structural equation modeling for causal analyses to assess mediation effects.

Main Results:

  • Children of mothers with IPV-PTSD exhibited significantly reduced PLE compared to controls, suggesting cortical hyper-arousal.
  • Child PLE was negatively correlated with maternal IPV-PTSD severity and child PTSD symptoms.
  • Causal analyses confirmed that child PLE mediates the relationship between maternal PTSD severity and child PTSD.

Conclusions:

  • Maternal IPV-PTSD is associated with altered child brain activity, specifically reduced PLE, indicating hyper-arousal.
  • Child PLE serves as a potential neurobiological marker mediating the intergenerational transmission of PTSD risk.
  • Findings support the development of targeted psycho-neurobehavioral therapies, such as neurofeedback, for affected families.

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