Please use this identifier to cite or link to this item: https://swslhd.intersearch.com.au/swslhdjspui/handle/1/12602
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dc.contributor.authorGriffiths, K. R.-
dc.contributor.authorBreukelaar, I. A.-
dc.contributor.authorHarvie, G.-
dc.contributor.authorYang, J.-
dc.contributor.authorFoster, S. L.-
dc.contributor.authorHarris, A. W.-
dc.contributor.authorClarke, S.-
dc.contributor.authorHay, P. J.-
dc.contributor.authorTouyz, S.-
dc.contributor.authorKorgaonkar, M. S.-
dc.contributor.authorKohn, M. R.-
dc.date.accessioned2024-03-11T01:57:30Z-
dc.date.available2024-03-11T01:57:30Z-
dc.date.issued2024-
dc.identifier.issn26671743 (ISSN)-
dc.identifier.urihttps://swslhd.intersearch.com.au/swslhdjspui/handle/1/12602-
dc.description.abstractBackground: Speculation exists as to whether lisdexamfetamine dimesylate (LDX) acts on the functional connectivity (FC) of brain networks that modulate appetite, reward, or inhibitory control in binge-eating disorder (BED). Better insights into its action may help guide the development of more targeted therapeutics and identify who will benefit most from this medication. Here, we use a comprehensive data-driven approach to investigate the brain FC changes that underlie the therapeutic action of LDX in patients with BED. Methods: Forty-six participants with moderate to severe BED received LDX titrated to 50 or 70 mg for an 8-week period. Twenty age-matched healthy control participants were also recruited. Resting-state functional magnetic resonance imaging was used to probe changes in brain FC pre- and post treatment and correlated with change in clinical measures. Results: Ninety-seven percent of trial completers (n = 31) experienced remission or a reduction to mild BED during the 8-week LDX trial. Widespread neural FC changes occurred, with changes in default mode to limbic, executive control to subcortical, and default mode to executive control networks associated with improvements in clinical outcomes. These connections were not distinct from control participants at pretreatment but were different from control participants following LDX treatment. Pretreatment connectivity did not predict treatment response. Conclusions: FC between networks associated with self-referential processing, executive function, and reward seem to underlie the therapeutic effect of LDX in BED. This suggests that LDX activates change via multiple systems, with most changes in compensatory networks rather than in those characterizing the BED diagnosis. � 2023 The Authors-
dc.publisherElsevier Inc.-
dc.subjectBinge-eating disorder Clinical trial Data-driven Default mode network Functional connectivity Lisdexamfetamine adult Article binge eating disorder clinical article clinical outcome controlled clinical trial controlled study disease severity drug dose increase drug dose titration drug effect drug efficacy executive function executive network female functional magnetic resonance imaging human male remission treatment duration treatment response-
dc.titleFunctional Connectivity Mechanisms Underlying Symptom Reduction Following Lisdexamfetamine Treatment in Binge-Eating Disorder: A Clinical Trial-
dc.typeJournal Article-
dc.contributor.swslhdauthorHay, Phillipa-
dc.description.affiliatesBrain Dynamics Centre, Westmead Institute for Medical Research, The University of Sydney, Westmead, NSW, Australia InsideOut Institute, University of Sydney, Sydney Local Health District, Sydney, NSW, Australia School of Psychology, University of New South Wales, Sydney, NSW, Australia Department of Radiology, Westmead Hospital, Sydney, NSW, Australia Specialty of Psychiatry, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia Centre for Research into Adolescents? Health, University of Sydney, Sydney, NSW, Australia Adolescent and Young Adult Medicine, Westmead Hospital, Sydney, NSW, Australia Translational Health Research Institute, School of Medicine, Western Sydney University, Sydney, NSW, Australia Mental Health Services, Camden and Campbelltown Hospitals, South Western Sydney Local Health District, Sydney, NSW, Australia Clinical Psychology Unit, School of Psychology, University of Sydney, Sydney, NSW, Australia-
dc.identifier.doi10.1016/j.bpsgos.2023.08.016-
dc.identifier.departmentCamden and Campbelltown Hospitals, Department of Mental Health Research-
dc.type.studyortrialArticle-
dc.identifier.journaltitleBiological Psychiatry Global Open Science-
Appears in Collections:Camden and Campbelltown Hospitals
South Western Sydney Local Health District

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