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Effects of PPP1R1B (DARPP-32) Polymorphism on Feedback-Related Brain Potentials Across the Life Span

Maximizing gains during probabilistic reinforcement learning requires the updating of choice – outcome expectations at the time when the feedback about a specific choice or action is given. Extant theories and evidence suggest that dopaminergic modulation plays a crucial role in reinforcement learni...

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Autores principales: Hämmerer, Dorothea, Biele, Gudio, Müller, Viktor, Thiele, Holger, Nürnberg, Peter, Heekeren, Hauke R., Li, Shu-Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586677/
https://www.ncbi.nlm.nih.gov/pubmed/23459765
http://dx.doi.org/10.3389/fpsyg.2013.00089
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author Hämmerer, Dorothea
Biele, Gudio
Müller, Viktor
Thiele, Holger
Nürnberg, Peter
Heekeren, Hauke R.
Li, Shu-Chen
author_facet Hämmerer, Dorothea
Biele, Gudio
Müller, Viktor
Thiele, Holger
Nürnberg, Peter
Heekeren, Hauke R.
Li, Shu-Chen
author_sort Hämmerer, Dorothea
collection PubMed
description Maximizing gains during probabilistic reinforcement learning requires the updating of choice – outcome expectations at the time when the feedback about a specific choice or action is given. Extant theories and evidence suggest that dopaminergic modulation plays a crucial role in reinforcement learning and the updating of choice – outcome expectations. Furthermore, recently a positive component of the event-related potential about 200 ms (P2) after feedback has been suggested to reflect such updating. The efficacy of dopaminergic modulation changes across the life span. However, to date investigations of age-related differences in feedback-related P2 during reinforcement learning are still scarce. The present study thus aims to investigate whether individual differences in the feedback-related P2 would be associated with polymorphic variations in a dopamine relevant gene PPP1R1B (also known as DARPP-32) and whether the genetic effect may differ between age groups. We observed larger P2 amplitudes in individuals carrying the genotype associated with higher dopamine receptor efficacy, i.e., a allele homozygotes of a single nucleotide polymorphism (rs907094) of the PPP1R1B gene. Moreover, this effect was more pronounced in children and older adults in comparison to adolescents and younger adults. Together, our findings indicate that polymorphic variations in a dopamine relevant gene are associated with individual differences in brain-evoked potentials of outcome updating and hint at the possibility that genotype effects on neurocognitive phenotypes may vary as a function of brain maturation and aging.
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spelling pubmed-35866772013-03-04 Effects of PPP1R1B (DARPP-32) Polymorphism on Feedback-Related Brain Potentials Across the Life Span Hämmerer, Dorothea Biele, Gudio Müller, Viktor Thiele, Holger Nürnberg, Peter Heekeren, Hauke R. Li, Shu-Chen Front Psychol Psychology Maximizing gains during probabilistic reinforcement learning requires the updating of choice – outcome expectations at the time when the feedback about a specific choice or action is given. Extant theories and evidence suggest that dopaminergic modulation plays a crucial role in reinforcement learning and the updating of choice – outcome expectations. Furthermore, recently a positive component of the event-related potential about 200 ms (P2) after feedback has been suggested to reflect such updating. The efficacy of dopaminergic modulation changes across the life span. However, to date investigations of age-related differences in feedback-related P2 during reinforcement learning are still scarce. The present study thus aims to investigate whether individual differences in the feedback-related P2 would be associated with polymorphic variations in a dopamine relevant gene PPP1R1B (also known as DARPP-32) and whether the genetic effect may differ between age groups. We observed larger P2 amplitudes in individuals carrying the genotype associated with higher dopamine receptor efficacy, i.e., a allele homozygotes of a single nucleotide polymorphism (rs907094) of the PPP1R1B gene. Moreover, this effect was more pronounced in children and older adults in comparison to adolescents and younger adults. Together, our findings indicate that polymorphic variations in a dopamine relevant gene are associated with individual differences in brain-evoked potentials of outcome updating and hint at the possibility that genotype effects on neurocognitive phenotypes may vary as a function of brain maturation and aging. Frontiers Media S.A. 2013-03-04 /pmc/articles/PMC3586677/ /pubmed/23459765 http://dx.doi.org/10.3389/fpsyg.2013.00089 Text en Copyright © 2013 Hämmerer, Biele, Müller, Thiele, Nürnberg, Heekeren and Li. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Psychology
Hämmerer, Dorothea
Biele, Gudio
Müller, Viktor
Thiele, Holger
Nürnberg, Peter
Heekeren, Hauke R.
Li, Shu-Chen
Effects of PPP1R1B (DARPP-32) Polymorphism on Feedback-Related Brain Potentials Across the Life Span
title Effects of PPP1R1B (DARPP-32) Polymorphism on Feedback-Related Brain Potentials Across the Life Span
title_full Effects of PPP1R1B (DARPP-32) Polymorphism on Feedback-Related Brain Potentials Across the Life Span
title_fullStr Effects of PPP1R1B (DARPP-32) Polymorphism on Feedback-Related Brain Potentials Across the Life Span
title_full_unstemmed Effects of PPP1R1B (DARPP-32) Polymorphism on Feedback-Related Brain Potentials Across the Life Span
title_short Effects of PPP1R1B (DARPP-32) Polymorphism on Feedback-Related Brain Potentials Across the Life Span
title_sort effects of ppp1r1b (darpp-32) polymorphism on feedback-related brain potentials across the life span
topic Psychology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586677/
https://www.ncbi.nlm.nih.gov/pubmed/23459765
http://dx.doi.org/10.3389/fpsyg.2013.00089
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