DAT1 polymorphism is associated with risk taking in the Balloon Analogue Risk Task (BART).

Twin-studies suggest that a significant portion of individual differences in the propensity to take risks resides in people's genetic make-up and there is evidence that variability in dopaminergic systems relates to individual differences in risky choice. We examined the link between risk takin...

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Main Authors: Rui Mata, Robin Hau, Andreas Papassotiropoulos, Ralph Hertwig
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22723947/?tool=EBI
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spelling doaj-f707f8635e144de6bcc01610b544f3352021-03-03T20:28:41ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0176e3913510.1371/journal.pone.0039135DAT1 polymorphism is associated with risk taking in the Balloon Analogue Risk Task (BART).Rui MataRobin HauAndreas PapassotiropoulosRalph HertwigTwin-studies suggest that a significant portion of individual differences in the propensity to take risks resides in people's genetic make-up and there is evidence that variability in dopaminergic systems relates to individual differences in risky choice. We examined the link between risk taking in a risk taking task (the Balloon Analogue Risk Task, BART) and a variable number tandem repeat (VNTR) polymorphism in the 3'UTR of the dopamine transporter gene (SLC6A3/DAT1). Behavior in BART is known to be associated with activity in striatal reward-processing regions, and DAT1 is assumed to modulate striatal dopamine levels. We find that carriers of DAT1 alleles, which presumably result in lower striatal dopamine availability, showed more risk taking, relative to carriers of the alleles associated with higher striatal dopamine availability. Our analyses suggest that the mechanism underlying this association is diminished sensitivity to rewards among those who take more risks. Overall, our results support the notion that a behavioral genetic approach can be helpful in uncovering the basis of individual differences in risk taking.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22723947/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Rui Mata
Robin Hau
Andreas Papassotiropoulos
Ralph Hertwig
spellingShingle Rui Mata
Robin Hau
Andreas Papassotiropoulos
Ralph Hertwig
DAT1 polymorphism is associated with risk taking in the Balloon Analogue Risk Task (BART).
PLoS ONE
author_facet Rui Mata
Robin Hau
Andreas Papassotiropoulos
Ralph Hertwig
author_sort Rui Mata
title DAT1 polymorphism is associated with risk taking in the Balloon Analogue Risk Task (BART).
title_short DAT1 polymorphism is associated with risk taking in the Balloon Analogue Risk Task (BART).
title_full DAT1 polymorphism is associated with risk taking in the Balloon Analogue Risk Task (BART).
title_fullStr DAT1 polymorphism is associated with risk taking in the Balloon Analogue Risk Task (BART).
title_full_unstemmed DAT1 polymorphism is associated with risk taking in the Balloon Analogue Risk Task (BART).
title_sort dat1 polymorphism is associated with risk taking in the balloon analogue risk task (bart).
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Twin-studies suggest that a significant portion of individual differences in the propensity to take risks resides in people's genetic make-up and there is evidence that variability in dopaminergic systems relates to individual differences in risky choice. We examined the link between risk taking in a risk taking task (the Balloon Analogue Risk Task, BART) and a variable number tandem repeat (VNTR) polymorphism in the 3'UTR of the dopamine transporter gene (SLC6A3/DAT1). Behavior in BART is known to be associated with activity in striatal reward-processing regions, and DAT1 is assumed to modulate striatal dopamine levels. We find that carriers of DAT1 alleles, which presumably result in lower striatal dopamine availability, showed more risk taking, relative to carriers of the alleles associated with higher striatal dopamine availability. Our analyses suggest that the mechanism underlying this association is diminished sensitivity to rewards among those who take more risks. Overall, our results support the notion that a behavioral genetic approach can be helpful in uncovering the basis of individual differences in risk taking.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22723947/?tool=EBI
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