Context
Abnormalities in associative memory processes, such as Pavlovian fear conditioning and extinction, have been observed in schizophrenia. The retrieval of fear extinction memories (‘safety signals’) may be particularly affected; although schizophrenia patients can extinguish conditioned fear, they show a deficit in retrieving fear extinction memories after a delay. The neurobiological basis of this abnormality is unknown, but clues have emerged from studies in rodents and humans demonstrating that the ventromedial prefrontal cortex (vmPFC) is a key mediator of extinction memory retrieval.
Objective
To measure autonomic and neural responses during the acquisition and extinction of conditioned fear and the delayed recall of fear and extinction memories in patients with schizophrenia and healthy controls.
Design
Cross-sectional case-control, functional magnetic resonance imaging study.
Setting
Academic medical center.
Participants
Twenty patients with schizophrenia and 17 healthy control participants, demographically-matched to the patient group.
Main Outcome Measures
Skin conductance and blood oxygen level dependent (BOLD) responses.
Results
During fear conditioning, patients with schizophrenia showed blunted autonomic responses and abnormal BOLD responses, relative to controls, within the posterior cingulate gyrus, hippocampus and other regions. Several of these abnormalities were linked to negative symptoms. During extinction learning, patients with schizophrenia and controls showed comparable autonomic and neural responses. Twenty-four hours after the learning phases, the control subjects exhibited decreased fear and increased vmPFC responses in the extinction (safe) context as expected, indicating successful retention of the extinction memory. In contrast, the schizophrenia patients showed inappropriately elevated fear and poor vmPFC responses in the safe context.
Conclusion
Failure of extinction memory retrieval in schizophrenia is associated with vmPFC dysfunction. In future studies, abnormalities in fear learning and extinction recall may serve as quantitative phenotypes that can be linked to genetic, symptom or outcome profiles in schizophrenia and those at risk for the disorder.