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Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration.
Document Type
article
Author
Olney, Nicholas TOng, EliseGoh, Sheng-Yang MBajorek, LynnDever, ReillyStaffaroni, Adam MCobigo, YannBock, MeredithChiang, KevinLjubenkov, PeterKornak, JohnHeuer, Hilary WWang, PingRascovsky, KatyaWolf, AmeliaAppleby, BrianBove, JessicaBordelon, YvetteBrannelly, PatrickBrushaber, DanielleCaso, ChristineCoppola, GiovanniDickerson, Bradford CDickinson, SusanDomoto-Reilly, KimikoFaber, KellyFerrall, JessicaFields, JulieFishman, AnnFong, JamieForoud, TatianaForsberg, Leah KGearhart, Debra JGhazanfari, BehnazGhoshal, NupurGoldman, JillGraff-Radford, JonathanGraff-Radford, Neill RGrant, IanGrossman, MurrayHaley, DanaHsiung, GingyuekHuey, Edward DIrwin, David JJones, David TKantarci, KejalKarydas, Anna MKaufer, DanielKerwin, DianaKnopman, David SKramer, Joel HKraft, RuthKremers, WalterKukull, WalterLapid, Maria ILitvan, IreneMackenzie, Ian RMaldonado, MirandaManoochehri, MasoodMcGinnis, Scott MMcKinley, Emily CMendez, Mario FMiller, Bruce LOnyike, ChiadiPantelyat, AlexPearlman, RodneyPetrucelli, LenPotter, MadeleineRademakers, RosaRamos, Eliana MRankin, Katherine PRoberson, Erik DRogalski, EmilySengdy, PhethShaw, Leslie MSyrjanen, JeremyTartaglia, M CarmelaTatton, NadineTaylor, JoanneToga, ArthurTrojanowski, John QWeintraub, SandraWong, BonnieWszolek, ZbigniewBoxer, Adam LBoeve, Brad FRosen, Howard JARTFL and LEFFTDS consortia
Source
Alzheimer's & dementia : the journal of the Alzheimer's Association. 16(1)
Subject
ARTFL and LEFFTDS consortia
Temporal Lobe
Humans
Atrophy
Genetic Predisposition to Disease
tau Proteins
Magnetic Resonance Imaging
Longitudinal Studies
Neuropsychological Tests
Image Processing
Computer-Assisted
Middle Aged
Female
Male
Frontotemporal Lobar Degeneration
C9orf72 Protein
Progranulins
C9ORF72
Familial
Frontotemporal lobar degeneration
GRN
Genetic
MAPT
Frontotemporalobar degeneration
Neurodegenerative
Behavioral and Social Science
Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD)
Alzheimer's Disease Related Dementias (ADRD)
Biomedical Imaging
Aging
Alzheimer's Disease
Clinical Trials and Supportive Activities
Acquired Cognitive Impairment
Dementia
Clinical Research
Brain Disorders
Neurosciences
Rare Diseases
Frontotemporal Dementia (FTD)
2.1 Biological and endogenous factors
Neurological
Geriatrics
Clinical Sciences
Language
Abstract
IntroductionThe Advancing Research and Treatment in Frontotemporal Lobar Degeneration and Longitudinal Evaluation of Familial Frontotemporal Dementia Subjects longitudinal studies were designed to describe the natural history of familial-frontotemporal lobar degeneration due to autosomal dominant mutations.MethodsWe examined cognitive performance, behavioral ratings, and brain volumes from the first time point in 320 MAPT, GRN, and C9orf72 family members, including 102 non-mutation carriers, 103 asymptomatic carriers, 43 mildly/questionably symptomatic carriers, and 72 carriers with dementia.ResultsAsymptomatic carriers showed similar scores on all clinical measures compared with noncarriers but reduced frontal and temporal volumes. Those with mild/questionable impairment showed decreased verbal recall, fluency, and Trail Making Test performance and impaired mood and self-monitoring. Dementia was associated with impairment in all measures. All MAPT carriers with dementia showed temporal atrophy, but otherwise, there was no single cognitive test or brain region that was abnormal in all subjects.DiscussionImaging changes appear to precede clinical changes in familial-frontotemporal lobar degeneration, but specific early clinical and imaging changes vary across individuals.