Related Experiment Videos
P300 and genetic risk for schizophrenia
Georg Winterer1, Michael F Egan, Thomas Raedler
1Clinical Brain Disorders Branch, National Institute of Mental Health, National Institutes of Health, Building 10, Room 4s229A, MSC 1379, Bethesda, MD 20892, USA. wintereg@intra.nimh.nih.gov
Archives of General Psychiatry
|November 12, 2003
Summary
Event-related potential P300 amplitude changes in the frontal and temporoparietal regions may serve as useful quantitative phenotypes for schizophrenia genetics. These findings enhance statistical power in genetic studies of schizophrenia risk.
Area of Science:
- Neuroscience
- Psychiatry
- Genetics
Background:
- Investigating event-related potential (ERP) P300 changes as intermediate phenotypes for schizophrenia genetics.
- Addressing limitations of previous studies that did not identify localized P300 changes predicting schizophrenia risk.
Purpose of the Study:
- To assess the suitability of frontal and temporoparietal P300 changes as intermediate phenotypes in genetic studies of schizophrenia.
- To utilize principal component analysis for understanding widespread cortical generator networks in P300 abnormalities.
Main Methods:
- Studied P300 changes in schizophrenic patients, their healthy siblings, and unrelated controls using an auditory oddball paradigm.
- Calculated principal components for frontal and temporoparietal P300 amplitude and latency.
- Determined intraclass correlations (ICCs) and relative risk ratios (lambda) for P300 components between sib-pairs.
Main Results:
- Schizophrenic patients and siblings showed reduced temporoparietal P300 amplitude and increased frontal P300 amplitude compared to controls.
- Significant ICCs and increased relative risk ratios were observed for both frontal and temporoparietal P300 amplitude components.
Conclusions:
- Temporoparietal P300 amplitude reduction and frontal P300 amplitude increase are quantitative phenotypes linked to schizophrenia risk.
- These P300 amplitude measures can potentially increase statistical power in genetic studies of schizophrenia.