Title of article
Variations in the Catechol O-methyltransferase Polymorphism and Prefrontally Guided Behaviors in Adolescents
Author/Authors
Dustin Wahlstrom، نويسنده , , Tonya White، نويسنده , , Catalina J. Hooper، نويسنده , , Suzanne Vrshek-Schallhorn، نويسنده , , William S. Oetting، نويسنده , , Marcia J. Brott، نويسنده , , Monica Luciana، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2007
Pages
7
From page
626
To page
632
Abstract
Background
The catechol-O-methyltransferase (COMT) gene codes for an enzyme that degrades prefrontal cortex (PFC) synaptic dopamine. Of two identified alleles (Met and Val), the Met allele results in COMT activity that is up to 4 times less pronounced than that conferred by the Val allele, resulting in greater PFC dopamine concentrations. Met-Met homozygotes perform better than individuals who possess the Val allele on PFC-mediated cognitive tasks. These genotypic variations and their associations with executive functions have been described in adults and prepubescent children, but there is a paucity of research assessing these relations in adolescent samples.
Methods
In this study, 70 children aged 9–17 were genotyped for COMT and completed measures of working memory, attention, fine motor coordination, and motor speed.
Results
COMT genotype modulated all but the motor speed measures. The Val-Met genotype was optimal for performance in this adolescent sample.
Conclusions
Results are discussed within the context of developmental changes in the dopaminergic system during adolescence.
Keywords
Neuropsychology , prefrontalcortex , genetics , cognition , Adolescence , Dopamine
Journal title
Biological Psychiatry
Serial Year
2007
Journal title
Biological Psychiatry
Record number
503285
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