دورية أكاديمية

Neural activation of regions involved in food reward and cognitive control in young females with anorexia nervosa and atypical anorexia nervosa versus healthy controls.

التفاصيل البيبلوغرافية
العنوان: Neural activation of regions involved in food reward and cognitive control in young females with anorexia nervosa and atypical anorexia nervosa versus healthy controls.
المؤلفون: Eddy KT; Eating Disorders Clinical and Research Program, Massachusetts General Hospital, Boston, MA, USA. keddy@mgh.harvard.edu.; Department of Psychiatry, Harvard Medical School, Boston, MA, USA. keddy@mgh.harvard.edu., Plessow F; Neuroendocrine Unit, Massachusetts General Hospital, Boston, MA, USA.; Department of Medicine, Harvard Medical School, Boston, MA, USA., Breithaupt L; Eating Disorders Clinical and Research Program, Massachusetts General Hospital, Boston, MA, USA.; Department of Psychiatry, Harvard Medical School, Boston, MA, USA., Becker KR; Eating Disorders Clinical and Research Program, Massachusetts General Hospital, Boston, MA, USA.; Department of Psychiatry, Harvard Medical School, Boston, MA, USA., Slattery M; Neuroendocrine Unit, Massachusetts General Hospital, Boston, MA, USA., Mancuso CJ; Neuroendocrine Unit, Massachusetts General Hospital, Boston, MA, USA., Izquierdo AM; Neuroendocrine Unit, Massachusetts General Hospital, Boston, MA, USA., Van De Water AL; Neuroendocrine Unit, Massachusetts General Hospital, Boston, MA, USA.; Division of Women's Health, Department of Medicine, and Department of Psychiatry, Brigham and Women's Hospital, Boston, MA, USA., Kahn DL; Neuroendocrine Unit, Massachusetts General Hospital, Boston, MA, USA., Dreier MJ; Eating Disorders Clinical and Research Program, Massachusetts General Hospital, Boston, MA, USA., Ebrahimi S; Cambridge Eating Disorders Center, Cambridge, MA, USA., Deckersbach T; Department of Psychiatry, Harvard Medical School, Boston, MA, USA.; University of Applied Sciences, Diploma Hochschule, Bad Sooden-Allendorf, Germany., Thomas JJ; Eating Disorders Clinical and Research Program, Massachusetts General Hospital, Boston, MA, USA.; Department of Psychiatry, Harvard Medical School, Boston, MA, USA., Holsen LM; Department of Psychiatry, Harvard Medical School, Boston, MA, USA.; Division of Women's Health, Department of Medicine, and Department of Psychiatry, Brigham and Women's Hospital, Boston, MA, USA., Misra M; Neuroendocrine Unit, Massachusetts General Hospital, Boston, MA, USA.; Department of Medicine, Harvard Medical School, Boston, MA, USA.; Division of Pediatric Endocrinology, Mass General for Children, Boston, MA, USA., Lawson EA; Neuroendocrine Unit, Massachusetts General Hospital, Boston, MA, USA.; Department of Medicine, Harvard Medical School, Boston, MA, USA.
المصدر: Translational psychiatry [Transl Psychiatry] 2023 Jun 23; Vol. 13 (1), pp. 220. Date of Electronic Publication: 2023 Jun 23.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Nature Pub. Group Country of Publication: United States NLM ID: 101562664 Publication Model: Electronic Cited Medium: Internet ISSN: 2158-3188 (Electronic) Linking ISSN: 21583188 NLM ISO Abbreviation: Transl Psychiatry Subsets: MEDLINE
أسماء مطبوعة: Original Publication: New York, NY : Nature Pub. Group
مواضيع طبية MeSH: Anorexia Nervosa*/diagnostic imaging, Adolescent ; Female ; Humans ; Magnetic Resonance Imaging/methods ; Food ; Cognition ; Reward
مستخلص: 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.
(© 2023. The Author(s).)
References: Psychoneuroendocrinology. 2021 Jul;129:105243. (PMID: 34049199)
PLoS Comput Biol. 2018 Aug 24;14(8):e1006370. (PMID: 30142152)
Addict Biol. 2013 Sep;18(5):855-62. (PMID: 22974271)
Neuroimage. 2002 Jan;15(1):273-89. (PMID: 11771995)
Trends Neurosci. 2013 Feb;36(2):110-20. (PMID: 23333342)
Neuroimage. 2007 Aug 1;37(1):343-60. (PMID: 17553704)
Annu Rev Neurosci. 2016 Jul 8;39:149-70. (PMID: 27090954)
Appetite. 2015 Apr;87:98-107. (PMID: 25528694)
Eur Arch Psychiatry Clin Neurosci. 2004 Aug;254(4):245-51. (PMID: 15309395)
Neuropsychopharmacology. 2012 Aug;37(9):2031-46. (PMID: 22549118)
Neuropsychopharmacology. 2010 Jan;35(1):169-91. (PMID: 19625997)
Compr Psychiatry. 2014 Nov;55(8):1773-84. (PMID: 25214371)
Am J Psychiatry. 2008 Feb;165(2):245-50. (PMID: 18198267)
Brain Cogn. 2016 Dec;110:20-42. (PMID: 27156016)
Int J Obes (Lond). 2018 Apr;42(4):785-793. (PMID: 28894291)
Int J Obes (Lond). 2012 May;36(5):648-55. (PMID: 21712804)
Int J Eat Disord. 2018 Mar;51(3):250-261. (PMID: 29405338)
Proc Natl Acad Sci U S A. 2010 Aug 17;107(33):14811-6. (PMID: 20679212)
Neuroimage Clin. 2015 Mar 24;8:1-31. (PMID: 26110109)
Nat Neurosci. 2009 Jul;12(7):939-45. (PMID: 19503087)
Neurosci Biobehav Rev. 2022 Jul;138:104721. (PMID: 35667634)
Cell Metab. 2008 May;7(5):400-9. (PMID: 18460331)
Int J Eat Disord. 2023 Apr;56(4):798-820. (PMID: 36508318)
Biol Psychiatry. 2011 Oct 15;70(8):736-743. (PMID: 21714958)
Neuroimage. 2012 Mar;60(1):213-20. (PMID: 22230946)
Am J Clin Nutr. 2014 Jun;99(6):1319-30. (PMID: 24760977)
Biol Psychiatry. 2013 May 1;73(9):836-42. (PMID: 23380716)
Sci Rep. 2017 Feb 13;7:42066. (PMID: 28198813)
Am J Clin Nutr. 2012 Nov;96(5):989-99. (PMID: 22990034)
J Eat Disord. 2016 May 18;4:19. (PMID: 27195123)
J Eat Disord. 2018 Nov 1;6:31. (PMID: 30410758)
Biol Psychiatry. 2022 May 15;91(10):869-878. (PMID: 34593204)
J Clin Psychiatry. 2017 Feb;78(2):184-189. (PMID: 28002660)
Int J Eat Disord. 2021 Aug;54(8):1328-1357. (PMID: 33864277)
Soc Cogn Affect Neurosci. 2023 Feb 6;18(1):. (PMID: 33830272)
J Psychiatry Neurosci. 2012 Sep;37(5):322-32. (PMID: 22498079)
Psychiatr Clin North Am. 2019 Mar;42(1):75-91. (PMID: 30704641)
Psychol Med. 2010 Oct;40(10):1735-44. (PMID: 20047706)
Psychoneuroendocrinology. 2020 Mar;113:104556. (PMID: 31918391)
Int J Eat Disord. 2020 Apr;53(4):631-636. (PMID: 32198943)
Ann N Y Acad Sci. 2018 Sep;1428(1):208-220. (PMID: 29543993)
Curr Neuropharmacol. 2018;16(8):1150-1163. (PMID: 29046154)
J Clin Child Adolesc Psychol. 2022 Sep-Oct;51(5):715-725. (PMID: 35476589)
Psychoneuroendocrinology. 2020 Sep;119:104722. (PMID: 32512249)
Nat Neurosci. 2016 Apr 26;19(6):656-664. (PMID: 29162973)
Am J Clin Nutr. 2018 Feb 1;107(2):145-154. (PMID: 29529147)
Eur J Neurosci. 2009 Oct;30(8):1625-35. (PMID: 19811532)
Neuropsychopharmacology. 2018 Feb;43(3):638-645. (PMID: 28930284)
Science. 1997 Mar 14;275(5306):1593-9. (PMID: 9054347)
PLoS One. 2011;6(7):e22259. (PMID: 21799807)
Front Behav Neurosci. 2014 Dec 09;8:410. (PMID: 25538579)
معلومات مُعتمدة: MH103402 U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH); MH112485 U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH); MH111127 U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH); MH108595 U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH); MH103402 U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH); MH103402, MH108595, MH120568 U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH); DK040561 U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases)
تواريخ الأحداث: Date Created: 20230623 Date Completed: 20230626 Latest Revision: 20231116
رمز التحديث: 20240829
مُعرف محوري في PubMed: PMC10290133
DOI: 10.1038/s41398-023-02494-3
PMID: 37353543
قاعدة البيانات: MEDLINE
الوصف
تدمد:2158-3188
DOI:10.1038/s41398-023-02494-3