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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
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.
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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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