Holocaust Exposure Induced Intergenerational Effects on FKBP5 Methylation

• Published in: Biological psychiatry (1969) 2016-09, Vol.80 (5), p.372-380
• Main Authors: Yehuda, Rachel, Daskalakis, Nikolaos P, Bierer, Linda M, Bader, Heather N, Klengel, Torsten, Holsboer, Florian, Binder, Elisabeth B
• Format: Article
• Language: English
• Subjects: Adult Children - psychology; Child of Impaired Parents; Cohort Studies; Cortisol; Cytosine; DNA Methylation - genetics; Epigenetics; Female; FKBP5; Holocaust - psychology; Humans; Intergenerational; Male; Parents; Psychiatric Status Rating Scales; Psychiatry; PTSD; Stress; Stress Disorders, Post-Traumatic - genetics; Surveys and Questionnaires; Survivors - psychology; Tacrolimus Binding Proteins - genetics
• ISSN: 0006-3223; 1873-2402
• DOI: 10.1016/j.biopsych.2015.08.005

Abstract Background The involvement of epigenetic mechanisms in intergenerational transmission of stress effects has been demonstrated in animals but not in humans. Methods Cytosine methylation within the gene encoding for FK506 binding protein 5 (FKBP5) was measured in Holocaust survivors ( n = 32), their adult offspring ( n = 22), and demographically comparable parent ( n = 8) and offspring ( n = 9) control subjects, respectively. Cytosine-phosphate-guanine sites for analysis were chosen based on their spatial proximity to the intron 7 glucocorticoid response elements. Results Holocaust exposure had an effect on FKBP5 methylation that was observed in exposed parents as well in their offspring. These effects were observed at bin 3/site 6. Interestingly, in Holocaust survivors, methylation at this site was higher in comparison with control subjects, whereas in Holocaust offspring, methylation was lower. Methylation levels for exposed parents and their offspring were significantly correlated. In contrast to the findings at bin 3/site 6, offspring methylation at bin 2/sites 3 to 5 was associated with childhood physical and sexual abuse in interaction with an FKBP5 risk allele previously associated with vulnerability to psychological consequences of childhood adversity. The findings suggest the possibility of site specificity to environmental influences, as sites in bins 3 and 2 were differentially associated with parental trauma and the offspring’s own childhood trauma, respectively. FKBP5 methylation averaged across the three bins examined was associated with wake-up cortisol levels, indicating functional relevance of the methylation measures. Conclusions This is the first demonstration of an association of pre-conception parental trauma with epigenetic alterations that is evident in both exposed parent and offspring, providing potential insight into how severe psychophysiological trauma can have intergenerational effects.