Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16728
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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 LS-
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-
dc.contributor.authorCorreia, Stephen-
dc.contributor.authorSperling, Reisa A-
dc.contributor.authorChhatwal, Jasmeer P-
dc.contributor.authorMayeux, Richard-
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 Jr-
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.contributor.authorDominantly Inherited Alzheimer Network (DIAN)-
dc.date201-07-22-
dc.date.accessioned2017-07-26T01:12:31Z-
dc.date.available2017-07-26T01:12:31Z-
dc.date.issued2017-07-22-
dc.identifier.citationAlzheimer's & Dementia 2017; online first: 22 Julyen_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16728-
dc.description.abstractINTRODUCTION: Identifying at what point atrophy rates first change in Alzheimer's disease is important for informing design of presymptomatic trials. METHODS: Serial T1-weighed 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. RESULTS: 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. DISCUSSION: 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.en_US
dc.subjectAlzheimer's diseaseen_US
dc.subjectAtrophyen_US
dc.subjectAutosomal dominanten_US
dc.subjectBoundary Shift Integralen_US
dc.subjectChange-pointen_US
dc.subjectDementiaen_US
dc.subjectLongitudinalen_US
dc.subjectMRIen_US
dc.subjectNeuroimagingen_US
dc.subjectNonlinear modelingen_US
dc.titlePresymptomatic atrophy in autosomal dominant Alzheimer's disease: a serial MRI studyen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleAlzheimer's & Dementiaen_US
dc.identifier.affiliationDementia Research Centre, UCL Institute of Neurology, London, UKen_US
dc.identifier.affiliationTranslational Imaging Group, UCL Centre for Medical Image Computing, London, UKen_US
dc.identifier.affiliationLondon School of Hygiene & Tropical Medicine, London, UKen_US
dc.identifier.affiliationDepartment of Radiology, Washington University School of Medicine, St. Louis, MO, USAen_US
dc.identifier.affiliationDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USAen_US
dc.identifier.affiliationDepartment of Neurological Surgery & Psychiatry, Washington University School of Medicine, St. Louis, MO, USAen_US
dc.identifier.affiliationDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USAen_US
dc.identifier.affiliationBrown University-Butler Hospital, Providence, RI, USAen_US
dc.identifier.affiliationDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USAen_US
dc.identifier.affiliationDepartment of Neurology, Columbia University Medical Center, New York, NY, USAen_US
dc.identifier.affiliationSchool of Medical Sciences, Edith Cowan University, Joondalup, WA, Australiaen_US
dc.identifier.affiliationDepartment of Neurology, Indiana University School of Medicine, Indianapolis, IN, USAen_US
dc.identifier.affiliationDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN, USAen_US
dc.identifier.affiliationDepartment of Radiology and Imaging Sciences, Indiana University School of Medicine, Indianapolis, IN, USAen_US
dc.identifier.affiliationDepartment of Radiology, Mayo Clinic, Rochester, MN, USAen_US
dc.identifier.affiliationNeuroscience Research Australia, Randwick, NSW, Australiaen_US
dc.identifier.affiliationSchool of Medical Sciences, University of New South Wales, Sydney, NSW, Australiaen_US
dc.identifier.affiliationDepartment of Radiology, School of Medicine, University of California, San Francisco, San Francisco, CA, USAen_US
dc.identifier.affiliationDepartment of Neurology, Keck USC School of Medicine, Los Angeles, CA, USAen_US
dc.identifier.affiliationImaging Genetics Center, Keck School of Medicine, University of Southern California, Marina del Rey, CA, USAen_US
dc.identifier.affiliationThe Florey Institute, The University of Melbourne, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Nuclear Medicine and Centre for PET, Austin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/28738187en_US
dc.identifier.doi10.1016/j.jalz.2017.06.2268en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-3910-2453en_US
dc.type.austinJournal Articleen_US
local.name.researcherMasters, Colin L
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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