Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20947
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dc.contributor.authorKinnunen, Kirsi M-
dc.contributor.authorCash, David M-
dc.contributor.authorPoole, Teresa-
dc.contributor.authorFrost, Chris-
dc.contributor.authorBenzinger, Tammie L S-
dc.contributor.authorAhsan, R Laila-
dc.contributor.authorLeung, Kelvin K-
dc.contributor.authorCardoso, M Jorge-
dc.contributor.authorModat, Marc-
dc.contributor.authorMalone, Ian B-
dc.contributor.authorMorris, John C-
dc.contributor.authorBateman, Randall J-
dc.contributor.authorMarcus, Daniel S-
dc.contributor.authorGoate, Alison-
dc.contributor.authorSalloway, Stephen P-
dc.contributor.authorCorreia, Stephen-
dc.contributor.authorSperling, Reisa A-
dc.contributor.authorChhatwal, Jasmeer P-
dc.contributor.authorMayeux, Richard P-
dc.contributor.authorBrickman, Adam M-
dc.contributor.authorMartins, Ralph N-
dc.contributor.authorFarlow, Martin R-
dc.contributor.authorGhetti, Bernardino-
dc.contributor.authorSaykin, Andrew J-
dc.contributor.authorJack, Clifford R-
dc.contributor.authorSchofield, Peter R-
dc.contributor.authorMcDade, Eric-
dc.contributor.authorWeiner, Michael W-
dc.contributor.authorRingman, John M-
dc.contributor.authorThompson, Paul M-
dc.contributor.authorMasters, Colin L-
dc.contributor.authorRowe, Christopher C-
dc.contributor.authorRossor, Martin N-
dc.contributor.authorOurselin, Sebastien-
dc.contributor.authorFox, Nick C-
dc.date2017-
dc.date.available2019-06-05-
dc.date.issued2018-
dc.identifier.citationAlzheimer's & dementia : the journal of the Alzheimer's Association 2018; 14(1): 43-53-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20947-
dc.description.abstractIdentifying at what point atrophy rates first change in Alzheimer's disease is important for informing design of presymptomatic trials. Serial T1-weighted magnetic resonance imaging scans of 94 participants (28 noncarriers, 66 carriers) from the Dominantly Inherited Alzheimer Network were used to measure brain, ventricular, and hippocampal atrophy rates. For each structure, nonlinear mixed-effects models estimated the change-points when atrophy rates deviate from normal and the rates of change before and after this point. Atrophy increased after the change-point, which occurred 1-1.5 years (assuming a single step change in atrophy rate) or 3-8 years (assuming gradual acceleration of atrophy) before expected symptom onset. At expected symptom onset, estimated atrophy rates were at least 3.6 times than those before the change-point. Atrophy rates are pathologically increased up to seven years before "expected onset". During this period, atrophy rates may be useful for inclusion and tracking of disease progression.-
dc.language.isoeng-
dc.subjectAlzheimer's disease-
dc.subjectAtrophy-
dc.subjectAutosomal dominant-
dc.subjectBoundary Shift Integral-
dc.subjectChange-point-
dc.subjectDementia-
dc.subjectLongitudinal-
dc.subjectMRI-
dc.subjectNeuroimaging-
dc.subjectNonlinear modeling-
dc.titlePresymptomatic atrophy in autosomal dominant Alzheimer's disease: A serial magnetic resonance imaging study.-
dc.typeJournal Article-
dc.identifier.journaltitleAlzheimer's & dementia : the journal of the Alzheimer's Association-
dc.identifier.affiliationDepartment of Medical Statistics, London School of Hygiene & Tropical Medicine, London, UKen
dc.identifier.affiliationDepartment of Neurodegenerative Disease, Dementia Research Centre, UCL Institute of Neurology, London, UKen
dc.identifier.affiliationDepartment of Medical Physics and Bioengineering, Translational Imaging Group, Centre for Medical Image Computing, University College London, London, UKen
dc.identifier.affiliationDepartment of Neurology, Butler Hospital, Warren Alpert Medical School, Brown University, Providence, RI, USAen
dc.identifier.affiliationDepartment of Neurodegenerative Disease, Dementia Research Centre, UCL Institute of Neurology, London, UKen
dc.identifier.affiliationDepartment of Neurology, Columbia University Medical Center, New York, NY, USAen
dc.identifier.affiliationDepartment of Neurology, Indiana University School of Medicine, Indianapolis, IN, USAen
dc.identifier.affiliationDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN, USAen
dc.identifier.affiliationDepartment of Radiology and Imaging Sciences, Centre for Neuroimaging, Indiana University School of Medicine, Indianapolis, IN, USAen
dc.identifier.affiliationDepartment of Radiology, Mayo Clinic, Rochester, MN, USAen
dc.identifier.affiliationDepartment of Radiology, School of Medicine, University of California, San Francisco, San Francisco, CA, USAen
dc.identifier.affiliationDepartment of Neurology, Keck USC School of Medicine, Los Angeles, CA, USAen
dc.identifier.affiliationImaging Genetics Center, Stevens Neuroimaging & Informatics Institute, Keck School of Medicine, University of Southern California, Marina del Rey, CA, USAen
dc.identifier.affiliationSchool of Medical Sciences, University of New South Wales, Sydney, NSW, Australiaen
dc.identifier.affiliationNeuroscience Research Australia, Randwick, NSW, Australiaen
dc.identifier.affiliationThe Florey Institute, University of Melbourne, Parkville, Victoria, Australiaen
dc.identifier.affiliationCentre of Excellence for Alzheimer's Disease Research and Care, School of Exercise, Biomedical and Health Sciences, Edith Cowan University, Joondalup, WA, Australiaen
dc.identifier.affiliationDepartment of Radiology, Washington University School of Medicine, St. Louis, MO, USAen
dc.identifier.affiliationDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USAen
dc.identifier.affiliationDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USAen
dc.identifier.affiliationDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USAen
dc.identifier.affiliationDepartment of Nuclear Medicine and Centre for PET, Austin Health, Heidelberg, Victoria, Australia-
dc.identifier.doi10.1016/j.jalz.2017.06.2268-
dc.identifier.orcid0000-0003-3910-2453-
dc.identifier.pubmedid28738187-
dc.type.austinJournal Article-
dc.type.austinResearch Support, N.I.H., Extramural-
dc.type.austinResearch Support, Non-U.S. Gov't-
local.name.researcherMasters, Colin L
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptMolecular Imaging and Therapy-
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