Hippocampal dysfunction during declarative memory encoding in schizophrenia and effects of genetic liability
Tara Pirnia1, Roger P Woods1, Liberty S Hamilton2
1Department of Neurology, Ahmanson-Lovelace Brain Mapping Center, Geffen School of Medicine, and Jane and Terry Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, USA.
Schizophrenia impairs declarative memory encoding, with brain activity differences seen in patients and relatives. These changes in the medial temporal lobe memory system suggest both disease and genetic factors influence memory.
Area of Science:
- Neuroscience
- Cognitive Psychology
- Psychiatry
Background:
- Declarative memory (DM) deficits are common in schizophrenia and their relatives.
- Neural mechanisms of encoding and genetic influences on DM in schizophrenia are not fully understood.
Purpose of the Study:
- To investigate neural correlates of successful and unsuccessful memory encoding in schizophrenia patients, unaffected relatives, and controls.
- To explore the impact of genetic liability on medial temporal lobe (MTL) memory system function.
Main Methods:
- Event-related functional MRI (fMRI) was used to compare brain activations during face-name associative memory encoding.
- Participants included 26 schizophrenia patients, 30 controls, and 14 unaffected relatives.
- Regions-of-interest analysis focused on hippocampal activity and hippocampal volume.
Main Results:
- Schizophrenia patients exhibited hyper-activations in visual and temporo-parietal areas during successful encoding.
- Patients showed right anterior hippocampus hyper-activation and left anterior hippocampus hypo-activation during successful encoding.
- Unaffected relatives displayed similar left anterior hippocampus hypo-activations, suggesting genetic liability. Patients had reduced hippocampal volume, but relatives did not.
Conclusions:
- DM encoding deficits in schizophrenia involve both disease-specific and genetic liability factors affecting the MTL memory system.
- Hyper-activations in temporo-occipital and parietal regions indicate disease-related influences in patients.
- Shared hippocampal hypo-activations in patients and relatives point to genetic factors influencing memory encoding.
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