RESUMEN
The present study examined the genetic and environmental etiology of decision-making (Iowa Gambling Task; Bechara, Damásio, Damásio, & Anderson, 1994), in a sample of twins at ages 11-13, 14-15, and 16-18 years. The variance across five 20-trial blocks could be explained by a latent "decision-making'' factor within each of the three times of IGT administration. This latent factor was modestly influenced by genetic factors, explaining 35%, 20% and 46% of the variance within each of the three times of IGT administration. The remaining variance was explained by the non-shared environment (65%, 80% and 54%, respectively). Block-specific non-shared environmental influences were also observed. The stability of decision-making was modest across development. Youth showed a trend to choose less risky decks at later ages, suggesting some improvement in task performance across development. These findings contribute to our understanding of decision-making by highlighting the particular importance of each person's unique experiences on individual differences.
Asunto(s)
Toma de Decisiones , Interacción Gen-Ambiente , Adolescente , Análisis de Varianza , California , Niño , Femenino , Juego de Azar/genética , Humanos , Masculino , Modelos Genéticos , Estudios Prospectivos , Factores SexualesRESUMEN
The orienting response is a widely used experimental paradigm that reflects the association between electrodermal activity and psychological processes. The present study examined the genetic and environmental etiology of skin conductance orienting response (SCOR) magnitude in a sample of twins assessed at ages 9-10, 11-13 and 14-16 years. Structural equation modeling at each visit showed that genetic influences explained 56%, 83%, and 48% of the total variance in SCOR at visits 1, 2, and 3, respectively, with the remaining variance explained by non-shared environmental factors. SCOR was moderately stable across ages, with phenotypic correlations between time points ranging from .35 to .45. A common genetic factor explained 36%, 45% and 49% of the variance in SCOR magnitude across development. Additional age-specific genetic effects were found at ages 9-10 and 11-13 years, explaining 18% and 35% of the variance, respectively. The genetic correlations among the three time points were high, ranging from .55 to .73, indicating a substantial continuity in genetic influences from ages 9 to 16. These findings suggest that genetic factors are important influences in SCOR magnitude during late childhood and adolescence.