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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.
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.
Abstract:
This study examined whether there is a biological basis in the child's resting brain activity for the intergenerational link between maternal interpersonal violence-related posttraumatic stress disorder (IPV-PTSD) and child subclinical symptoms. We used high-density EEG recordings to investigate the resting brain activity in a sample of 57 children, 34 from mothers with IPV-PTSD, and 23 from mothers without PTSD. These children were part of a prospective, longitudinal study focusing on the offspring of mothers with and without IPV-PTSD, reporting how the severity of a mother's IPV-PTSD can impact her child's emotional regulation and risk for developing mental illness. However, we had not yet looked into potential EEG biomarkers during resting state that might mediate and/or moderate effects of maternal IPV-PTSD severity on child mental health, and in particular the risk for PTSD. The alpha band spectral power as well as the aperiodic exponent of the power spectrum (PLE; power-law exponent) were examined as mediators of maternal IPV-PTSD and child PTSD. While there was no difference in alpha spectral power between the two groups, PLE was significantly reduced in children of mothers with IPV-PTSD compared to control children, indicating cortical hyper-arousal. Interestingly, child PLE was negatively correlated with the severity of maternal IPV-PTSD, suggesting an intergenerational interaction. This interpretation was reinforced by a negative correlation between child PLE and child PTSD symptoms. Finally, causal analyses using structural equation modelling indicated that child PLE mediated the relationship between maternal PTSD severity and child PTSD. Our observations suggest that maternal IPV-PTSD has an intergenerational impact on the child neurobehavioral development through a correlated abnormal marker of brain arousal (i.e. child PLE). These findings are potentially relevant to psychotherapy research and to the development of more effective psycho-neurobehavioral therapies (i.e. neurofeedback) among affected individuals.
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