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Dopamine Genes (DRD2/ANKK1-TaqA1 and DRD4-7R) and Executive Function: Their Interaction with Obesity
Obesity is a multifactorial disease caused by the interaction between genotype and environment, and it is considered to be a type of addictive alteration. The A1 allele of the DRD2/ANKK1-TaqIA gene has been associated with addictive disorders, with obesity and with the performance in executive funct...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405092/ https://www.ncbi.nlm.nih.gov/pubmed/22848508 http://dx.doi.org/10.1371/journal.pone.0041482 |
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author | Ariza, Mar Garolera, Maite Jurado, Maria Angeles Garcia-Garcia, Isabel Hernan, Imma Sánchez-Garre, Consuelo Vernet-Vernet, Maria Sender-Palacios, Maria Jose Marques-Iturria, Idoia Pueyo, Roser Segura, Barbara Narberhaus, Ana |
author_facet | Ariza, Mar Garolera, Maite Jurado, Maria Angeles Garcia-Garcia, Isabel Hernan, Imma Sánchez-Garre, Consuelo Vernet-Vernet, Maria Sender-Palacios, Maria Jose Marques-Iturria, Idoia Pueyo, Roser Segura, Barbara Narberhaus, Ana |
author_sort | Ariza, Mar |
collection | PubMed |
description | Obesity is a multifactorial disease caused by the interaction between genotype and environment, and it is considered to be a type of addictive alteration. The A1 allele of the DRD2/ANKK1-TaqIA gene has been associated with addictive disorders, with obesity and with the performance in executive functions. The 7 repeat allele of the DRD4 gene has likewise been associated with the performance in executive functions, as well as with addictive behaviors and impulsivity. Participants were included in the obesity group (N = 42) if their body mass index (BMI) was equal to or above 30, and in the lean group (N = 42) if their BMI was below 25. The DRD2/ANKK1-TaqIA and DRD4 VNTR polymorphisms were obtained. All subjects underwent neuropsychological assessment. Eating behavior traits were evaluated. The ‘DRD2/ANKK1-TaqIA A1-allele status’ had a significant effect on almost all the executive variables, but no significant ‘DRD4 7R-allele status’ effects were observed for any of the executive variables analyzed. There was a significant ‘group’ x ‘DRD2/ANKK1-TaqIA A1-allele status’ interaction effect on LN and ‘group’ x ‘DRD4 7R-allele status’ interaction effect on TMT B-A score. Being obese and a carrier of the A1 allele of DRD2/ANKK1-TaqIA or the 7R allele of DRD4 VNTR polymorphisms could confer a weakness as regards the performance of executive functions. |
format | Online Article Text |
id | pubmed-3405092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34050922012-07-30 Dopamine Genes (DRD2/ANKK1-TaqA1 and DRD4-7R) and Executive Function: Their Interaction with Obesity Ariza, Mar Garolera, Maite Jurado, Maria Angeles Garcia-Garcia, Isabel Hernan, Imma Sánchez-Garre, Consuelo Vernet-Vernet, Maria Sender-Palacios, Maria Jose Marques-Iturria, Idoia Pueyo, Roser Segura, Barbara Narberhaus, Ana PLoS One Research Article Obesity is a multifactorial disease caused by the interaction between genotype and environment, and it is considered to be a type of addictive alteration. The A1 allele of the DRD2/ANKK1-TaqIA gene has been associated with addictive disorders, with obesity and with the performance in executive functions. The 7 repeat allele of the DRD4 gene has likewise been associated with the performance in executive functions, as well as with addictive behaviors and impulsivity. Participants were included in the obesity group (N = 42) if their body mass index (BMI) was equal to or above 30, and in the lean group (N = 42) if their BMI was below 25. The DRD2/ANKK1-TaqIA and DRD4 VNTR polymorphisms were obtained. All subjects underwent neuropsychological assessment. Eating behavior traits were evaluated. The ‘DRD2/ANKK1-TaqIA A1-allele status’ had a significant effect on almost all the executive variables, but no significant ‘DRD4 7R-allele status’ effects were observed for any of the executive variables analyzed. There was a significant ‘group’ x ‘DRD2/ANKK1-TaqIA A1-allele status’ interaction effect on LN and ‘group’ x ‘DRD4 7R-allele status’ interaction effect on TMT B-A score. Being obese and a carrier of the A1 allele of DRD2/ANKK1-TaqIA or the 7R allele of DRD4 VNTR polymorphisms could confer a weakness as regards the performance of executive functions. Public Library of Science 2012-07-25 /pmc/articles/PMC3405092/ /pubmed/22848508 http://dx.doi.org/10.1371/journal.pone.0041482 Text en Ariza et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Ariza, Mar Garolera, Maite Jurado, Maria Angeles Garcia-Garcia, Isabel Hernan, Imma Sánchez-Garre, Consuelo Vernet-Vernet, Maria Sender-Palacios, Maria Jose Marques-Iturria, Idoia Pueyo, Roser Segura, Barbara Narberhaus, Ana Dopamine Genes (DRD2/ANKK1-TaqA1 and DRD4-7R) and Executive Function: Their Interaction with Obesity |
title | Dopamine Genes (DRD2/ANKK1-TaqA1 and DRD4-7R) and Executive Function: Their Interaction with Obesity |
title_full | Dopamine Genes (DRD2/ANKK1-TaqA1 and DRD4-7R) and Executive Function: Their Interaction with Obesity |
title_fullStr | Dopamine Genes (DRD2/ANKK1-TaqA1 and DRD4-7R) and Executive Function: Their Interaction with Obesity |
title_full_unstemmed | Dopamine Genes (DRD2/ANKK1-TaqA1 and DRD4-7R) and Executive Function: Their Interaction with Obesity |
title_short | Dopamine Genes (DRD2/ANKK1-TaqA1 and DRD4-7R) and Executive Function: Their Interaction with Obesity |
title_sort | dopamine genes (drd2/ankk1-taqa1 and drd4-7r) and executive function: their interaction with obesity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405092/ https://www.ncbi.nlm.nih.gov/pubmed/22848508 http://dx.doi.org/10.1371/journal.pone.0041482 |
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