| Literature DB >> 28314160 |
Anne-Laure Aziz1, Bernard Giusiano2, Sven Joubert3, Lauréline Duprat4, Mira Didic5, Claude Gueriot6, Lejla Koric6, José Boucraut7, Olivier Felician5, Jean-Philippe Ranjeva4, Eric Guedj8, Mathieu Ceccaldi5.
Abstract
Neuroimaging biomarkers differ between patients with early-onset Alzheimer's disease (EOAD) and late-onset Alzheimer's disease (LOAD). Whether these changes reflect cognitive heterogeneity or differences in disease severity is still unknown. This study aimed at investigating changes in neuroimaging biomarkers, according to the age of onset of the disease, in mild amnestic Alzheimer's disease patients with positive amyloid biomarkers in cerebrospinal fluid. Both patient groups were impaired on tasks assessing verbal and visual recognition memory. EOAD patients showed greater executive and linguistic deficits, while LOAD patients showed greater semantic memory impairment. In EOAD and LOAD, hypometabolism involved the bilateral temporoparietal junction and the posterior cingulate cortex. In EOAD, atrophy was widespread, including frontotemporoparietal areas, whereas it was limited to temporal regions in LOAD. Atrophic volumes were greater in EOAD than in LOAD. Hypometabolic volumes were similar in the 2 groups. Greater extent of atrophy in EOAD, despite similar extent of hypometabolism, could reflect different underlying pathophysiological processes, different glucose-based compensatory mechanisms or distinct level of premorbid atrophic lesions.Entities:
Keywords: Age of onset; Alzheimer's disease; Magnetic resonance imaging; Neuroimaging biomarkers; Positron emission tomography imaging
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Year: 2017 PMID: 28314160 DOI: 10.1016/j.neurobiolaging.2017.02.010
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673