Presymptomatic atrophy in autosomal dominant Alzheimer's disease: A serial magnetic resonance imaging study

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.contributor.departmentNeurology, School of Medicineen_US
dc.date.accessioned2019-07-01T17:01:47Z
dc.date.available2019-07-01T17:01:47Z
dc.date.issued2018-01
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-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. 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.eprint.versionAuthor's manuscripten_US
dc.identifier.citationKinnunen, K. M., Cash, D. M., Poole, T., Frost, C., Benzinger, T., Ahsan, R. L., … Dominantly Inherited Alzheimer Network (DIAN) (2018). Presymptomatic atrophy in autosomal dominant Alzheimer's disease: A serial magnetic resonance imaging study. Alzheimer's & dementia : the journal of the Alzheimer's Association, 14(1), 43–53. doi:10.1016/j.jalz.2017.06.2268en_US
dc.identifier.urihttps://hdl.handle.net/1805/19771
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.jalz.2017.06.2268en_US
dc.relation.journalAlzheimer's & Dementia : the Journal of the Alzheimer's Associationen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectLongitudinalen_US
dc.subjectAtrophyen_US
dc.subjectAlzheimer’s diseaseen_US
dc.subjectDementiaen_US
dc.subjectAutosomal dominanten_US
dc.subjectNeuroimagingen_US
dc.subjectMRIen_US
dc.subjectBoundary Shift Integralen_US
dc.subjectNonlinear modelingen_US
dc.subjectChange-pointen_US
dc.titlePresymptomatic atrophy in autosomal dominant Alzheimer's disease: A serial magnetic resonance imaging studyen_US
dc.typeArticleen_US
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