Cargando…
Neural activation of regions involved in food reward and cognitive control in young females with anorexia nervosa and atypical anorexia nervosa versus healthy controls
Anorexia nervosa (AN) and atypical AN (AtypAN) are complex neurobiological illnesses that typically onset in adolescence with an often treatment-refractory and chronic illness trajectory. Aberrant eating behaviors in this population have been linked to abnormalities in food reward and cognitive cont...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290133/ https://www.ncbi.nlm.nih.gov/pubmed/37353543 http://dx.doi.org/10.1038/s41398-023-02494-3 |
_version_ | 1785062427010793472 |
---|---|
author | Eddy, Kamryn T. Plessow, Franziska Breithaupt, Lauren Becker, Kendra R. Slattery, Meghan Mancuso, Christopher J. Izquierdo, Alyssa M. Van De Water, Avery L. Kahn, Danielle L. Dreier, Melissa J. Ebrahimi, Seda Deckersbach, Thilo Thomas, Jennifer J. Holsen, Laura M. Misra, Madhusmita Lawson, Elizabeth A. |
author_facet | Eddy, Kamryn T. Plessow, Franziska Breithaupt, Lauren Becker, Kendra R. Slattery, Meghan Mancuso, Christopher J. Izquierdo, Alyssa M. Van De Water, Avery L. Kahn, Danielle L. Dreier, Melissa J. Ebrahimi, Seda Deckersbach, Thilo Thomas, Jennifer J. Holsen, Laura M. Misra, Madhusmita Lawson, Elizabeth A. |
author_sort | Eddy, Kamryn T. |
collection | PubMed |
description | Anorexia nervosa (AN) and atypical AN (AtypAN) are complex neurobiological illnesses that typically onset in adolescence with an often treatment-refractory and chronic illness trajectory. Aberrant eating behaviors in this population have been linked to abnormalities in food reward and cognitive control, but prior studies have not examined respective contributions of clinical characteristics and metabolic state. Research is needed to identify specific disruptions and inform novel intervention targets to improve outcomes. Fifty-nine females with AN (n = 34) or AtypAN (n = 25), ages 10–22 years, all ≤90% expected body weight, and 34 age-matched healthy controls (HC) completed a well-established neuroimaging food cue paradigm fasting and after a standardized meal, and we used ANCOVA models to investigate main and interaction effects of Group and Appetitive State on blood oxygenation level-dependent (BOLD) activation for the contrast of exposure to high-calorie food images minus objects. We found main effects of Group with greater BOLD activation in the dorsal anterior cingulate cortex (dACC), dorsolateral prefrontal cortex (DLPFC), hippocampus, caudate, and putamen for AN/AtypAN versus HC groups, and in the three-group model including AN, AtypAN, and HC (sub-)groups, where differences were primarily driven by greater activation in the AtypAN subgroup versus HC group. We found a main effect of Appetitive State with increased premeal BOLD activation in the hypothalamus, amygdala, nucleus accumbens, and caudate for models that included AN/AtypAN and HC groups, and in BOLD activation in the nucleus accumbens for the model that included AN, AtypAN, and HC (sub-)groups. There were no interaction effects of Group with Appetitive State for any of the models. Our findings demonstrate robust feeding-state independent group effects reflecting greater neural activation of specific regions typically associated with reward and cognitive control processing across AN and AtypAN relative to healthy individuals in this food cue paradigm. Differential activation of specific brain regions in response to the passive viewing of high-calorie food images may underlie restrictive eating behavior in this clinical population. |
format | Online Article Text |
id | pubmed-10290133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102901332023-06-25 Neural activation of regions involved in food reward and cognitive control in young females with anorexia nervosa and atypical anorexia nervosa versus healthy controls Eddy, Kamryn T. Plessow, Franziska Breithaupt, Lauren Becker, Kendra R. Slattery, Meghan Mancuso, Christopher J. Izquierdo, Alyssa M. Van De Water, Avery L. Kahn, Danielle L. Dreier, Melissa J. Ebrahimi, Seda Deckersbach, Thilo Thomas, Jennifer J. Holsen, Laura M. Misra, Madhusmita Lawson, Elizabeth A. Transl Psychiatry Article Anorexia nervosa (AN) and atypical AN (AtypAN) are complex neurobiological illnesses that typically onset in adolescence with an often treatment-refractory and chronic illness trajectory. Aberrant eating behaviors in this population have been linked to abnormalities in food reward and cognitive control, but prior studies have not examined respective contributions of clinical characteristics and metabolic state. Research is needed to identify specific disruptions and inform novel intervention targets to improve outcomes. Fifty-nine females with AN (n = 34) or AtypAN (n = 25), ages 10–22 years, all ≤90% expected body weight, and 34 age-matched healthy controls (HC) completed a well-established neuroimaging food cue paradigm fasting and after a standardized meal, and we used ANCOVA models to investigate main and interaction effects of Group and Appetitive State on blood oxygenation level-dependent (BOLD) activation for the contrast of exposure to high-calorie food images minus objects. We found main effects of Group with greater BOLD activation in the dorsal anterior cingulate cortex (dACC), dorsolateral prefrontal cortex (DLPFC), hippocampus, caudate, and putamen for AN/AtypAN versus HC groups, and in the three-group model including AN, AtypAN, and HC (sub-)groups, where differences were primarily driven by greater activation in the AtypAN subgroup versus HC group. We found a main effect of Appetitive State with increased premeal BOLD activation in the hypothalamus, amygdala, nucleus accumbens, and caudate for models that included AN/AtypAN and HC groups, and in BOLD activation in the nucleus accumbens for the model that included AN, AtypAN, and HC (sub-)groups. There were no interaction effects of Group with Appetitive State for any of the models. Our findings demonstrate robust feeding-state independent group effects reflecting greater neural activation of specific regions typically associated with reward and cognitive control processing across AN and AtypAN relative to healthy individuals in this food cue paradigm. Differential activation of specific brain regions in response to the passive viewing of high-calorie food images may underlie restrictive eating behavior in this clinical population. Nature Publishing Group UK 2023-06-23 /pmc/articles/PMC10290133/ /pubmed/37353543 http://dx.doi.org/10.1038/s41398-023-02494-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Eddy, Kamryn T. Plessow, Franziska Breithaupt, Lauren Becker, Kendra R. Slattery, Meghan Mancuso, Christopher J. Izquierdo, Alyssa M. Van De Water, Avery L. Kahn, Danielle L. Dreier, Melissa J. Ebrahimi, Seda Deckersbach, Thilo Thomas, Jennifer J. Holsen, Laura M. Misra, Madhusmita Lawson, Elizabeth A. Neural activation of regions involved in food reward and cognitive control in young females with anorexia nervosa and atypical anorexia nervosa versus healthy controls |
title | Neural activation of regions involved in food reward and cognitive control in young females with anorexia nervosa and atypical anorexia nervosa versus healthy controls |
title_full | Neural activation of regions involved in food reward and cognitive control in young females with anorexia nervosa and atypical anorexia nervosa versus healthy controls |
title_fullStr | Neural activation of regions involved in food reward and cognitive control in young females with anorexia nervosa and atypical anorexia nervosa versus healthy controls |
title_full_unstemmed | Neural activation of regions involved in food reward and cognitive control in young females with anorexia nervosa and atypical anorexia nervosa versus healthy controls |
title_short | Neural activation of regions involved in food reward and cognitive control in young females with anorexia nervosa and atypical anorexia nervosa versus healthy controls |
title_sort | neural activation of regions involved in food reward and cognitive control in young females with anorexia nervosa and atypical anorexia nervosa versus healthy controls |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290133/ https://www.ncbi.nlm.nih.gov/pubmed/37353543 http://dx.doi.org/10.1038/s41398-023-02494-3 |
work_keys_str_mv | AT eddykamrynt neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols AT plessowfranziska neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols AT breithauptlauren neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols AT beckerkendrar neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols AT slatterymeghan neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols AT mancusochristopherj neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols AT izquierdoalyssam neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols AT vandewateraveryl neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols AT kahndaniellel neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols AT dreiermelissaj neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols AT ebrahimiseda neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols AT deckersbachthilo neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols AT thomasjenniferj neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols AT holsenlauram neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols AT misramadhusmita neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols AT lawsonelizabetha neuralactivationofregionsinvolvedinfoodrewardandcognitivecontrolinyoungfemaleswithanorexianervosaandatypicalanorexianervosaversushealthycontrols |