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American Journal of Psychiatry· 2014Q1

Ebeveyn Travma Sonrası Stres Bozukluğunun (TSSB) Holokost Mağduru Çocuklarında Glukokortikoid Reseptör Geninin Epigenetik Düzenlenmesi Üzerindeki Etkileri

Influences of Maternal and Paternal PTSD on Epigenetic Regulation of the Glucocorticoid Receptor Gene in Holocaust Survivor Offspring

Rachel Yehuda, Nikolaos P. Daskalakis, Amy Lehrner, Frank Désarnaud ve diğerleri

Kısa özet

Holokost mağdurlarının babasında TSSB olan çocuklarda, annenin TSSB'si tarafından modifiye edilen glukokortikoid reseptör geni (GR-1F) DNA metilasyonunda değişiklikler gözlemlenmiştir.

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Ana noktalar

  • Holokost mağdurlarının çocuklarında, annede TSSB yokken babada TSSB olması durumunda daha yüksek GR-1F promoter metilasyonu görülür.
  • Hem anne hem de babada TSSB olan çocuklarda daha düşük GR-1F promoter metilasyonu gözlemlenir.
  • Daha düşük GR-1F promoter metilasyonu, daha fazla post-dexametazon kortizol baskılanması ile ilişkilidir.
  • Anne TSSB'si, baba TSSB'sinin GR-1F promoter metilasyonu ve klinik göstergeler üzerindeki etkilerini modifiye eder.

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Özet (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.

Yazarların özeti; kaynağından alınmıştır. American Journal of Psychiatry, 2014 · DOI ↗

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Alan: Davranışsal Sinirbilim

Behavioral NeuroscienceNeuroscience