Epigenetic modification of the glucocorticoid receptor gene is linked to traumatic memory and post-traumatic stress disorder risk in genocide survivors

摘要

Recent evidence suggests that altered expression and epigenetic modification of the glucocorticoid receptor gene (NR3C1) are related to the risk of post-traumatic stress disorder (PTSD). The underlying mechanisms, however, remain unknown. Because glucocorticoid receptor signaling is known to regulate emotional memory processes, particularly in men, epigenetic modifications of NR3C1mightaffect the strength oftraumatic memories. Here, we found thatincreased DNA methylation atthe NGFI-A (nerve growth factor-induced protein A) binding site of the NR3C1promoter was associated with less intrusive memory of the traumatic event and reduced PTSD risk in male, but not female survivors of the Rwandan genocide.NR3C1methylation was not significantly related to hyperarousal or avoidance symptoms. We further investigated the relationship between NR3C1methylation and memory functions in a neuroimaging study in healthy subjects. Increased NR3C1methylation-which was associated with lower NR3C1expression-was related to reduced picture recognition in male, but not female subjects. Furthermore, we found methylation-dependent differences in recognition memory-related brain activity in men. Together, these findings indicate that an epigenetic modification of the glucocorticoid receptor gene promoter is linked to interindividual and gender-specific differences in memory functions and PTSD risk.