Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33625
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dc.contributor.authorRavanfar, Parsa-
dc.contributor.authorRushmore, R Jarrett-
dc.contributor.authorLyall, Amanda E-
dc.contributor.authorCropley, Vanessa-
dc.contributor.authorMakris, Nikos-
dc.contributor.authorDesmond, Patricia-
dc.contributor.authorVelakoulis, Dennis-
dc.contributor.authorShenton, Martha E-
dc.contributor.authorBush, Ashley I-
dc.contributor.authorRossell, Susan L-
dc.contributor.authorPantelis, Christos-
dc.contributor.authorSyeda, Warda T-
dc.contributor.authorPhillipou, Andrea-
dc.date2023-
dc.date.accessioned2023-08-30T07:48:19Z-
dc.date.available2023-08-30T07:48:19Z-
dc.date.issued2023-08-21-
dc.identifier.citationJournal of Eating Disorders 2023-08-21; 11(1)en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33625-
dc.description.abstractAnorexia nervosa (AN) is a potentially fatal psychiatric condition, associated with structural brain changes such as gray matter volume loss. The pathophysiological mechanisms for these changes are not yet fully understood. Iron is a crucial element in the development and function of the brain. Considering the systemic alterations in iron homeostasis in AN, we hypothesized that brain iron would be altered as a possible factor associated with structural brain changes in AN. In this study, we used quantitative susceptibility mapping (QSM) magnetic resonance imaging to investigate brain iron in current AN (c-AN) and weight-restored AN compared with healthy individuals. Whole-brain voxel wise comparison was used to probe areas with possible group differences. Further, the thalamus, caudate nucleus, putamen, nucleus accumbens, hippocampus, and amygdala were selected as the regions of interest (ROIs) for ROI-based comparison of mean QSM values. Whole-brain voxel-wise and ROI-based comparison of QSM did not reveal any differences between groups. Exploratory analyses revealed a correlation between higher regional QSM (higher iron) and lower body mass index, higher illness severity, longer illness duration, and younger age at onset in the c-AN group. This study did not find evidence of altered brain iron in AN compared to healthy individuals. However, the correlations between clinical variables and QSM suggest a link between brain iron and weight status or biological processes in AN, which warrants further investigation.en_US
dc.language.isoeng-
dc.subjectAnorexia nervosaen_US
dc.subjectBrainen_US
dc.subjectIronen_US
dc.subjectMagnetic resonance imagingen_US
dc.subjectQuantitative susceptibility mappingen_US
dc.titleInvestigation of brain iron in anorexia nervosa, a quantitative susceptibility mapping study.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Eating Disordersen_US
dc.identifier.affiliationMelbourne Neuropsychiatry Centre, Department of Psychiatry, The University of Melbourne and Royal Melbourne Hospital, Level 3, Alan Gilbert Building, 161 Barry ST, Carlton South, VIC, 3053, Australia. sravanfar@student.unimelb.edu.au.;Psychiatry Neuroimaging Laboratory, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.en_US
dc.identifier.affiliationPsychiatry Neuroimaging Laboratory, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.;Department of Psychiatry, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.;Department of Psychiatry, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.en_US
dc.identifier.affiliationPsychiatry Neuroimaging Laboratory, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.;Center for Morphometric Analysis (CMA), Massachusetts General Hospital, Charlestown, MA, USA.en_US
dc.identifier.affiliationDepartment of Radiology, Royal Melbourne Hospital, University of Melbourne, Parkville, VIC, Australia.en_US
dc.identifier.affiliationNeuropsychiatry, The Royal Melbourne Hospital, Parkville, VIC, Australia.en_US
dc.identifier.affiliationPsychiatry Neuroimaging Laboratory, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.;Department of Psychiatry, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.;Department of Radiology, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA, USA.en_US
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC, Australia.en_US
dc.identifier.affiliationCentre for Mental Health and Brain Sciences, Swinburne University, Hawthorn, VIC, Australia.;Department of Mental Health, St Vincent's Hospital, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationMelbourne Neuropsychiatry Centre, Department of Psychiatry, The University of Melbourne and Royal Melbourne Hospital, Level 3, Alan Gilbert Building, 161 Barry ST, Carlton South, VIC, 3053, Australia.;The Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC, Australia.en_US
dc.identifier.affiliationDepartment of Mental Health, St Vincent's Hospital, Melbourne, VIC, Australia.;Orygen, Melbourne, Australia.;Centre for Youth Mental Health, The University of Melbourne, Melbourne, Australia.;Department of Psychological Sciences, Swinburne University of Technology, Melbourne, Australia.en_US
dc.identifier.affiliationMental Healthen_US
dc.identifier.doi10.1186/s40337-023-00870-4en_US
dc.type.contentTexten_US
dc.identifier.pubmedid37605216-
dc.description.volume11-
dc.description.issue1-
dc.description.startpage142-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptMental Health-
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