Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/27544
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dc.contributor.authorChua P.en
dc.contributor.authorGeorgiou-Karistianis N.en
dc.contributor.authorEgan G.F.en
dc.contributor.authorGray M.A.en
dc.contributor.authorDominguez D J.F.en
dc.contributor.authorDymowski A.R.en
dc.contributor.authorBohanna I.en
dc.contributor.authorJohnston L.A.en
dc.contributor.authorStout J.C.en
dc.contributor.authorChurchyard A.en
dc.date.accessioned2021-05-14T09:16:28Zen
dc.date.available2021-05-14T09:16:28Zen
dc.date.copyright2013en
dc.date.created20130204en
dc.date.issued2013-02-04en
dc.identifier.citationNeurobiology of Disease. 51 (pp 82-92), 2013. Date of Publication: March 2013.en
dc.identifier.issn0969-9961en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/27544en
dc.description.abstractWe investigated two measures of neural integrity, T1-weighted volumetric measures and diffusion tensor imaging (DTI), and explored their combined potential to differentiate pre-diagnosis Huntington's disease (pre-HD) individuals from healthy controls. We applied quadratic discriminant analysis (QDA) to discriminate pre-HD individuals from controls and we utilised feature selection and dimension reduction to increase the robustness of the discrimination method. Thirty six symptomatic HD (symp-HD), 35 pre-HD, and 36 control individuals participated as part of the IMAGE-HD study and underwent T1-weighted MRI, and DTI using a Siemens 3. Tesla scanner. Volume and DTI measures [mean diffusivity (MD) and fractional anisotropy (FA)] were calculated for each group within five regions of interest (ROI; caudate, putamen, pallidum, accumbens and thalamus). QDA was then performed in a stepwise manner to differentiate pre-HD individuals from controls, based initially on unimodal analysis of motor or neurocognitive measures, or on volume, MD or FA measures from within the caudate, pallidum and putamen. We then tested for potential improvements to this model, by examining multi-modal MRI classifications (volume, FA and MD), and also included motor and neurocognitive measures, and additional brain regions (i.e., accumbens and thalamus). Volume, MD and FA differed across the three groups, with pre-HD characterised by significant volumetric reductions and increased FA within caudate, putamen and pallidum, relative to controls. The QDA results demonstrated that the differentiation of pre-HD from controls was highly accurate when both volumetric and diffusion data sets from basal ganglia (BG) regions were used. The highest discriminative accuracy however was achieved in a multi-modality approach and when including all available measures: motor and neurocognitive scores and multi-modal MRI measures from the BG, accumbens and thalamus. Our QDA findings provide evidence that combined multi-modal imaging measures can accurately classify individuals up to 15. years prior to onset when therapeutic intervention is likely to have maximal effects in slowing the trajectory of disease development. © 2012 Elsevier Inc.en
dc.languageEnglishen
dc.languageenen
dc.publisherAcademic Press Inc. (1250 Sixth Avenue, San Diego, California CA 92101, United States)en
dc.titleAutomated differentiation of pre-diagnosis Huntington's disease from healthy control individuals based on quadratic discriminant analysis of the basal ganglia: The IMAGE-HD study.en
dc.typeArticleen
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1016/j.nbd.2012.10.001en
dc.publisher.placeUnited Statesen
dc.identifier.pubmedid23069680 [http://www.ncbi.nlm.nih.gov/pubmed/?term=23069680]en
dc.identifier.source52347453en
dc.identifier.institution(Georgiou-Karistianis, Gray, Dominguez D, Dymowski, Chua, Stout, Egan) School of Psychology and Psychiatry, Faculty of Medicine Nursing and Health Sciences, Monash University, Clayton, VIC 3800, Australia (Gray, Egan) Monash Biomedical Imaging (MBI), Monash University, Melbourne, VIC 3800, Australia (Bohanna) School of Public Health, Tropical Medicine and Rehabilitation Sciences, James Cook University, Cairns, QLD 4870, Australia (Johnston, Egan) Howard Florey Institute, Florey Neuroscience Institutes, Parkville, VIC 30105, Australia (Johnston) Department of Electrical and Electronic Engineering, University of Melbourne, Parkville, VIC 3052, Australia (Churchyard) Department of Neurology, Monash Medical Centre, Clayton, VIC 3168, Australia (Egan) Centre for Neuroscience, University of Melbourne, Parkville, VIC 3010, Australia (Gray) Centre for Advanced Imaging, Gehrmann Laboratory, The University of Queensland, St Lucia, 4072, Australia (Gray) The University of Queensland Centre for Clinical Research, Royal Brisbane and Women's Hospital, Herston, 4029, Australiaen
dc.description.addressN. Georgiou-Karistianis, Experimental Neuropsychology Research Unit, School of Psychology and Psychiatry, Faculty of Medicine Nursing and Health Sciences, Monash University, Clayton, VIC 3800, Australia. E-mail: nellie.georgiou-karistianis@monash.eduen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2013 Elsevier B.V., All rights reserved.en
dc.subect.keywordsBasal ganglia Diffusion weighted imaging Fractional anisotropy Huntington's disease Magnetic resonance imaging Mean diffusivity Multivariate classification Quadratic discriminant function analysis T1-weighted volumeen
dc.identifier.authoremailGeorgiou-Karistianis N.; nellie.georgiou-karistianis@monash.eduen
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item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptMental Health-
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