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1.
Conscious Cogn ; 42: 1-8, 2016 05.
Artículo en Inglés | MEDLINE | ID: mdl-26954487

RESUMEN

Flow is a special mental state characterized by deep concentration that occurs during the performance of optimally challenging tasks. In prior studies, proneness to experience flow has been found to be moderately heritable. In the present study, we investigated whether individual differences in flow proneness are related to a polymorphism of the dopamine D2 receptor coding gene (DRD2 C957T rs6277). This polymorphism affects striatal D2 receptor availability, a factor that has been shown to be related to flow proneness. To our knowledge, this is the first study to investigate the association between this trait and a specific gene variant. In a sample of 236 healthy Hungarian adults, we found that CC homozygotes report higher flow proneness than do T allele carriers, but only during mandatory activities (i.e., studying and working), not during leisure time. We discuss implications of this result, e.g., the potential mediators of the relationship.


Asunto(s)
Atención/fisiología , Individualidad , Receptores de Dopamina D2/genética , Análisis y Desempeño de Tareas , Adulto , Femenino , Humanos , Masculino , Adulto Joven
2.
Neuropsychopharmacol Hung ; 14(4): 252-8, 2012 Dec.
Artículo en Húngaro | MEDLINE | ID: mdl-23269212

RESUMEN

Impairment of executive control functions in depression is well documented, and performance on the Stroop Test is one of the most widely used markers to measure the decline. This tool provides reliable quantitative phenotype data that can be used efficiently in candidate gene studies investigating inherited components of executive control. Aim of the present review is to summarize research on genetic factors of Stroop performance. Interestingly, only a few such candidate gene studies have been carried out to date. Twin studies show a 30-60% heritability estimate for the Stroop test, suggesting a significant genetic component. A single genome-wide association study has been carried out on Stroop performance, and it did not show any significant association with any of the tested polymorphisms after correction for multiple testing. Candidate gene studies to date pointed to the polymorphisms of several neurotransmitter systems (dopamine, serotonin, acetylcholine) and to the role of the APOE ε4 allele. Surprisingly, little is known about the genetic role of neurothrophic factors and survival factors. In conclusion, further studies are needed for clarifying the genetic background of Stroop performance, characterizing attentional functions.


Asunto(s)
Atención , Trastornos del Conocimiento/genética , Función Ejecutiva , Polimorfismo Genético , Desempeño Psicomotor , Test de Stroop , Apolipoproteína A-I/genética , Apolipoproteína C-III/genética , Apolipoproteínas E/genética , Factor Neurotrófico Derivado del Encéfalo/genética , Proteína C-Reactiva/genética , Trastornos del Conocimiento/metabolismo , Trastornos del Conocimiento/psicología , Dopamina/genética , Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil/genética , Predisposición Genética a la Enfermedad , Estudio de Asociación del Genoma Completo , Humanos , Proteína Huntingtina , Proteínas del Tejido Nervioso/genética , Neurotransmisores/genética , Polimorfismo de Nucleótido Simple , Receptores Nicotínicos/genética , Serotonina/genética , Estatmina/genética
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