Memory control ability modulates intrusive memories after analogue trauma

- Retrieval suppression predicts less distressing intrusive memories.
- ERP correlates of retrieval suppression predict less distressing intrusive memories.
- ERP correlates of retrieval suppression predict reduced impact of analogue trauma.

BackgroundMost people suffer from intrusive memories in the aftermath of trauma. For survivors' well-being, it is key that these intrusions are controlled. Memory control can be exerted through retrieval suppression. Poor retrieval suppression, however, should be associated with persistent distressing intrusions and posttraumatic stress disorder (PTSD). This study tested the hypothesis that individual differences in retrieval suppression predict intrusive memories after trauma. Retrieval suppression was examined with the think/no-think task (TNT) using behavioral and event related potential (ERP) measures.MethodsTwenty-four healthy participants watched a “traumatic” film after performing the TNT task. The frequency and distress of intrusions from the “traumatic” film was measured with an electronic diary. Additionally the Impact of Event Scale (IES) was assessed.ResultsIn line with our hypothesis, behavioral measures of retrieval suppression ability predicted reduced distress ratings for intrusions (r=−.53, p<.01). Further ERP markers of retrieval suppression (a fronto-centrally distributed N2) predicted reduced distress ratings for intrusions (r=−.45, p<.05) and reduced IES Intrusion scores (r=−.56, p<.01).LimitationsThe presented film is a relatively mild stressor as compared to a real-life trauma. Further studies are needed to explore the role of memory control processes for real-life trauma.ConclusionsParticipants with lower retrieval suppression ability exhibited less distressing intrusive memories after analogue trauma. The ERP correlate of retrieval suppression was associated with less distressing intrusive memories and reduced IES Intrusion scores, suggesting that deficient memory control is a potential risk factor for developing PTSD.