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DRD4 polymorphism associated with greater positive affect in response to negative and neutral social stimuli
Despite the robustness of DRD4 polymorphism associations with brain‐based behavioral characteristics in candidate gene research, investigations have minimally explored associations between these polymorphisms and emotional responses. In particular, the prevalent single nucleotide polymorphism (SNP)...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321090/ https://www.ncbi.nlm.nih.gov/pubmed/35574658 http://dx.doi.org/10.1111/ahg.12471 |
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author | Gilman, T. Lee Ford, Matthew T. Jasnow, Aaron M. Coifman, Karin G. |
author_facet | Gilman, T. Lee Ford, Matthew T. Jasnow, Aaron M. Coifman, Karin G. |
author_sort | Gilman, T. Lee |
collection | PubMed |
description | Despite the robustness of DRD4 polymorphism associations with brain‐based behavioral characteristics in candidate gene research, investigations have minimally explored associations between these polymorphisms and emotional responses. In particular, the prevalent single nucleotide polymorphism (SNP) ‐521C/T (rs1800955) in the promoter region of DRD4 remains unexplored relative to emotions. Here, two independent samples were evaluated using different emotion elicitation tasks involving social stimuli: Study 1 (N = 120) evoked positive and negative emotional responses to validated film clips; Study 2 (N = 122) utilized Cyberball to simulate social rejection and acceptance. Across studies, C/C individuals self‐reported higher mean positive affect scores using Likert scales versus T carrier individuals, selectively when presented with neutral or negative (but not positive) social stimuli. The consistent findings across these two studies supports a functional consequence of this DRD4 SNP on emotion processing during changing social contexts. Continued investigation will help clarify if a C/C genotype enhances positive emotions under negative circumstances, or if the presence of the T allele reduces positive emotions, and how rs1800955 behavioral associations might generalize across different demographics. Future studies could also reveal if this SNP interacts with other changing environmental conditions to affect emotional responses, such as social limitations during the COVID‐19 pandemic. |
format | Online Article Text |
id | pubmed-9321090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93210902022-07-30 DRD4 polymorphism associated with greater positive affect in response to negative and neutral social stimuli Gilman, T. Lee Ford, Matthew T. Jasnow, Aaron M. Coifman, Karin G. Ann Hum Genet Short Communication Despite the robustness of DRD4 polymorphism associations with brain‐based behavioral characteristics in candidate gene research, investigations have minimally explored associations between these polymorphisms and emotional responses. In particular, the prevalent single nucleotide polymorphism (SNP) ‐521C/T (rs1800955) in the promoter region of DRD4 remains unexplored relative to emotions. Here, two independent samples were evaluated using different emotion elicitation tasks involving social stimuli: Study 1 (N = 120) evoked positive and negative emotional responses to validated film clips; Study 2 (N = 122) utilized Cyberball to simulate social rejection and acceptance. Across studies, C/C individuals self‐reported higher mean positive affect scores using Likert scales versus T carrier individuals, selectively when presented with neutral or negative (but not positive) social stimuli. The consistent findings across these two studies supports a functional consequence of this DRD4 SNP on emotion processing during changing social contexts. Continued investigation will help clarify if a C/C genotype enhances positive emotions under negative circumstances, or if the presence of the T allele reduces positive emotions, and how rs1800955 behavioral associations might generalize across different demographics. Future studies could also reveal if this SNP interacts with other changing environmental conditions to affect emotional responses, such as social limitations during the COVID‐19 pandemic. John Wiley and Sons Inc. 2022-05-16 2022-07 /pmc/articles/PMC9321090/ /pubmed/35574658 http://dx.doi.org/10.1111/ahg.12471 Text en © 2022 The Authors. Annals of Human Genetics published by University College London (UCL) and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Short Communication Gilman, T. Lee Ford, Matthew T. Jasnow, Aaron M. Coifman, Karin G. DRD4 polymorphism associated with greater positive affect in response to negative and neutral social stimuli |
title |
DRD4 polymorphism associated with greater positive affect in response to negative and neutral social stimuli |
title_full |
DRD4 polymorphism associated with greater positive affect in response to negative and neutral social stimuli |
title_fullStr |
DRD4 polymorphism associated with greater positive affect in response to negative and neutral social stimuli |
title_full_unstemmed |
DRD4 polymorphism associated with greater positive affect in response to negative and neutral social stimuli |
title_short |
DRD4 polymorphism associated with greater positive affect in response to negative and neutral social stimuli |
title_sort | drd4 polymorphism associated with greater positive affect in response to negative and neutral social stimuli |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321090/ https://www.ncbi.nlm.nih.gov/pubmed/35574658 http://dx.doi.org/10.1111/ahg.12471 |
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