Abstract | OBJECTIVE: METHOD: Predictive pursuit and closed-loop gains of 62 patients with schizophrenia and 53 healthy comparison subjects with Val-Val, Val-Met, and Met-Met genotypes were compared. RESULTS: There was a significant diagnosis-by-genotype interaction: patients with the Met-Met genotype showed poor predictive pursuit. The Met-Met genotype in healthy subjects was associated with significantly higher predictive pursuit gain values than the Val-Val genotype in healthy subjects. The COMT genotype explained about 10% of the variance in each group's predictive pursuit performance. DISCUSSION: These preliminary data suggest that the COMT gene is associated with predictive eye tracking performance in healthy subjects. Predictive pursuit abnormality in schizophrenia is not attributable to the Val allele. These findings suggest a complex interaction with other etiological factors (e.g., another gene), and/or with prefrontal cortical dopaminergic activity.
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Authors | Gunvant K Thaker, Ikwunga Wonodi, Matthew T Avila, L Elliot Hong, O Colin Stine |
Journal | The American journal of psychiatry
(Am J Psychiatry)
Vol. 161
Issue 12
Pg. 2320-2
(Dec 2004)
ISSN: 0002-953X [Print] United States |
PMID | 15569909
(Publication Type: Comparative Study, Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Methionine
- Catechol O-Methyltransferase
- Valine
- Dopamine
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Topics |
- Adult
- Catechol O-Methyltransferase
(genetics, metabolism)
- Dopamine
(physiology)
- Genotype
- Humans
- Methionine
(genetics)
- Ocular Motility Disorders
(diagnosis, genetics)
- Polymorphism, Genetic
- Prefrontal Cortex
(physiology)
- Pursuit, Smooth
(genetics, physiology)
- Schizophrenia
(diagnosis, enzymology, genetics)
- Valine
(genetics)
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