American Journal of Psychiatry· 2014Q1
Influences of Maternal and Paternal PTSD on Epigenetic Regulation of the Glucocorticoid Receptor Gene in Holocaust Survivor Offspring
- 509citations
- Q1SCImago
- 2014year
Short summary
Offspring of Holocaust survivors with paternal PTSD show altered DNA methylation of the glucocorticoid receptor gene (GR-1F), with this effect moderated by maternal PTSD.
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Key points
- Paternal PTSD in Holocaust offspring is associated with higher GR-1F promoter methylation when maternal PTSD is absent.
- Offspring with both maternal and paternal PTSD show lower GR-1F promoter methylation.
- Lower GR-1F promoter methylation correlates with greater post-dexamethasone cortisol suppression.
- Maternal PTSD moderates the effects of paternal PTSD on GR-1F promoter methylation and clinical indicators.
AI-generated from the title and abstract; the full text is not read.
Abstract
OBJECTIVE: Differential effects of maternal and paternal posttraumatic stress disorder (PTSD) have been observed in adult offspring of Holocaust survivors in both glucocorticoid receptor sensitivity and vulnerability to psychiatric disorder. The authors examined the relative influences of maternal and paternal PTSD on DNA methylation of the exon 1F promoter of the glucocorticoid receptor (GR-1F) gene (NR3C1) in peripheral blood mononuclear cells and its relationship to glucocorticoid receptor sensitivity in Holocaust offspring. METHOD: Adult offspring with at least one Holocaust survivor parent (N=80) and demographically similar participants without parental Holocaust exposure or parental PTSD (N=15) completed clinical interviews, self-report measures, and biological procedures. Blood samples were collected for analysis of GR-1F promoter methylation and of cortisol levels in response to low-dose dexamethasone, and two-way analysis of covariance was performed using maternal and paternal PTSD as main effects. Hierarchical clustering analysis was used to permit visualization of maternal compared with paternal PTSD effects on clinical variables and GR-1F promoter methylation. RESULTS: A significant interaction demonstrated that in the absence of maternal PTSD, offspring with paternal PTSD showed higher GR-1F promoter methylation, whereas offspring with both maternal and paternal PTSD showed lower methylation. Lower GR-1F promoter methylation was significantly associated with greater postdexamethasone cortisol suppression. The clustering analysis revealed that maternal and paternal PTSD effects were differentially associated with clinical indicators and GR-1F promoter methylation. CONCLUSIONS: This is the first study to demonstrate alterations of GR-1F promoter methylation in relation to parental PTSD and neuroendocrine outcomes. The moderation of paternal PTSD effects by maternal PTSD suggests different mechanisms for the intergenerational transmission of trauma-related vulnerabilities.
The authors' abstract, as published at the source. American Journal of Psychiatry, 2014 · DOI ↗
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Field: Behavioral Neuroscience
Behavioral NeuroscienceNeuroscience