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Divergent neural substrates of inhibitory control in binge eating disorder relative to other manifestations of obesity
An important endeavor involves increasing our understanding of biobehavioral processes underlying different types of obesity. The current study investigated the neural correlates of cognitive control (involving conflict monitoring and response inhibition) in obese individuals with binge eating disor...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3610836/ https://www.ncbi.nlm.nih.gov/pubmed/23404820 http://dx.doi.org/10.1002/oby.20068 |
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author | Balodis, Iris M. Molina, Nathan D. Kober, Hedy Worhunsky, Patrick D. White, Marney A. Sinha, Rajita Grilo, Carlos M. Potenza, Marc N. |
author_facet | Balodis, Iris M. Molina, Nathan D. Kober, Hedy Worhunsky, Patrick D. White, Marney A. Sinha, Rajita Grilo, Carlos M. Potenza, Marc N. |
author_sort | Balodis, Iris M. |
collection | PubMed |
description | An important endeavor involves increasing our understanding of biobehavioral processes underlying different types of obesity. The current study investigated the neural correlates of cognitive control (involving conflict monitoring and response inhibition) in obese individuals with binge eating disorder (BED) as compared to BMI-matched non-BED obese (OB) individuals and lean comparison (LC) participants. Alterations in cognitive control may contribute to differences in behavioral control over eating behaviors in BED and obesity. Participants underwent functional magnetic resonance imaging (fMRI) while completing the Stroop color-word interference task. Relative to the OB and LC groups, activity in the BED group was differentiated by relative hypoactivity in brain areas involved in self-regulation and impulse control. Specifically, the BED group showed diminished activity in the ventromedial prefrontal cortex (vmPFC), inferior frontal gyrus (IFG) and insula during Stroop performance. In addition, dietary restraint scores were negatively correlated with right IFG and vmPFC activation in the BED group, but not in the OB or HC groups. Thus, BED individuals’ diminished ability to recruit impulse-control-related brain regions appears associated with impaired dietary restraint. The observed differences in neural correlates of inhibitory processing in BED relative to OB and LC groups suggest distinct neurobiological contributions to binge eating as a subgroup of obese individuals. |
format | Online Article Text |
id | pubmed-3610836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-36108362013-08-01 Divergent neural substrates of inhibitory control in binge eating disorder relative to other manifestations of obesity Balodis, Iris M. Molina, Nathan D. Kober, Hedy Worhunsky, Patrick D. White, Marney A. Sinha, Rajita Grilo, Carlos M. Potenza, Marc N. Obesity (Silver Spring) Article An important endeavor involves increasing our understanding of biobehavioral processes underlying different types of obesity. The current study investigated the neural correlates of cognitive control (involving conflict monitoring and response inhibition) in obese individuals with binge eating disorder (BED) as compared to BMI-matched non-BED obese (OB) individuals and lean comparison (LC) participants. Alterations in cognitive control may contribute to differences in behavioral control over eating behaviors in BED and obesity. Participants underwent functional magnetic resonance imaging (fMRI) while completing the Stroop color-word interference task. Relative to the OB and LC groups, activity in the BED group was differentiated by relative hypoactivity in brain areas involved in self-regulation and impulse control. Specifically, the BED group showed diminished activity in the ventromedial prefrontal cortex (vmPFC), inferior frontal gyrus (IFG) and insula during Stroop performance. In addition, dietary restraint scores were negatively correlated with right IFG and vmPFC activation in the BED group, but not in the OB or HC groups. Thus, BED individuals’ diminished ability to recruit impulse-control-related brain regions appears associated with impaired dietary restraint. The observed differences in neural correlates of inhibitory processing in BED relative to OB and LC groups suggest distinct neurobiological contributions to binge eating as a subgroup of obese individuals. 2013-02 /pmc/articles/PMC3610836/ /pubmed/23404820 http://dx.doi.org/10.1002/oby.20068 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Balodis, Iris M. Molina, Nathan D. Kober, Hedy Worhunsky, Patrick D. White, Marney A. Sinha, Rajita Grilo, Carlos M. Potenza, Marc N. Divergent neural substrates of inhibitory control in binge eating disorder relative to other manifestations of obesity |
title | Divergent neural substrates of inhibitory control in binge eating disorder relative to other manifestations of obesity |
title_full | Divergent neural substrates of inhibitory control in binge eating disorder relative to other manifestations of obesity |
title_fullStr | Divergent neural substrates of inhibitory control in binge eating disorder relative to other manifestations of obesity |
title_full_unstemmed | Divergent neural substrates of inhibitory control in binge eating disorder relative to other manifestations of obesity |
title_short | Divergent neural substrates of inhibitory control in binge eating disorder relative to other manifestations of obesity |
title_sort | divergent neural substrates of inhibitory control in binge eating disorder relative to other manifestations of obesity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3610836/ https://www.ncbi.nlm.nih.gov/pubmed/23404820 http://dx.doi.org/10.1002/oby.20068 |
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