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Visual sensory processing deficits in patients with bipolar disorder revealed through high-density electrical mapping
Sherlyn Yeap1, Simon P Kelly, Richard B Reilly
1The Cognitive Neurophysiology Laboratory, St. Vincent's Hospital, Richmond Road, Fairview, Dublin, Republic of Ireland.
Journal of Psychiatry & Neuroscience : JPN
|December 2, 2009
Summary
Patients with bipolar disorder exhibit reduced P1 visual evoked potential (VEP) amplitude, indicating early visual processing deficits similar to those in schizophrenia. This finding suggests a potential shared genetic liability for psychosis.
Area of Science:
- Neuroscience
- Psychiatry
- Genetics
Background:
- Bipolar disorder and schizophrenia share etiological commonalities, including auditory processing deficits.
- Schizophrenia patients show visual sensory processing deficits, but this is unconfirmed in bipolar disorder.
Purpose of the Study:
- To investigate early visual sensory processing deficits in bipolar disorder patients.
- To compare visual evoked potential (VEP) P1 component amplitude in bipolar disorder with schizophrenia findings.
- To explore the P1 deficit as a potential endophenotype for common genetic liability.
Main Methods:
- Euthymic bipolar disorder patients and healthy controls underwent visual presentation of isolated-check stimuli.
- A simple go/no-go task was employed during high-density electroencephalography (72-channel) recording of VEPs.
Main Results:
- A substantial reduction in P1 VEP amplitude was observed in bipolar disorder patients.
- The observed effect size (f = 0.56) indicates a large effect, consistent with Cohen's criteria.
Conclusions:
- Reduced P1 amplitude in bipolar disorder signifies early visual processing dysfunction, mirroring schizophrenia findings.
- This P1 deficit may be a broader indicator of psychosis development and a candidate endophenotype for bipolar disorder.
- Further research is warranted to explore the P1 deficit's relation to psychosis susceptibility genes.