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. 2011 Mar;41(2):175-83.
doi: 10.1007/s10519-010-9384-7. Epub 2010 Aug 11.

Heritability of delay discounting in adolescence: a longitudinal twin study

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Heritability of delay discounting in adolescence: a longitudinal twin study

Andrey P Anokhin et al. Behav Genet. 2011 Mar.

Abstract

Delay discounting (DD) refers to the preference for smaller immediate rewards over larger but delayed rewards, and is considered to be a distinct component of a broader "impulsivity" construct. Although greater propensity for discounting the value of delayed gratification has been associated with a range of problem behaviors and substance abuse, particularly in adolescents, the origins of individual differences in DD remain unclear. We examined genetic and environmental influences on a real-life behavioral measure of DD using a longitudinal twin design. Adolescent participants were asked to choose between a smaller ($7) reward available immediately and a larger ($10) reward to be received in 7 days. Biometrical genetic analysis using linear structural equation modeling showed significant heritability of DD at ages 12 and 14 (30 and 51%, respectively) and suggested that the same genetic factors influenced the trait at both ages. DD was significantly associated with symptoms of conduct disorder, attention deficit hyperactivity disorder, substance use, and with higher novelty seeking and poor self-regulation. This study provides the first evidence for heritability of DD in humans and suggests that DD can be a promising endophenotype for genetic studies of addiction and externalizing disorders.

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Figures

Fig. 1
Fig. 1
Path diagram for the best-fitting structural equation model. The paths retained in the model along with the estimated path coefficients are shown in black, and the paths that could be dropped without significant deterioration of fit are shown in grey. Rectangles represent the observed phenotype (choice of immediate versus delayed reward) measured at ages 12 and 14; circles represent the corresponding latent additive genetic, non-additive genetic, and non-shared environmental factors (A, D, and E, respectively). Standardized parameter estimates are shown for each path retained in the final model

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