| Literature DB >> 29203090 |
Miranka Wirth1, Alexandre Bejanin2, Renaud La Joie2, Eider M Arenaza-Urquijo2, Julie Gonneaud2, Brigitte Landeau2, Audrey Perrotin3, Florence Mézenge2, Vincent de La Sayette3, Béatrice Desgranges3, Gaël Chételat4.
Abstract
Alzheimer's disease (AD) is characterized by the presence of β-amyloid (Aβ) deposition and neurodegeneration. To seek for signs of such pathologies, we compared regional biomarker degrees and patterns of Aβ deposition, glucose hypometabolism, and gray matter volume (GMV) reduction in 3 groups at risk of AD. In elderly carriers of the apolipoprotein E ε4 (APOE4, n = 17), patients with subjective cognitive decline (n = 16), and patients with mild cognitive impairment (n = 30), head-to-head intermodality comparisons were performed on cross-sectional structural magnetic resonance images as well as 18F-fluorodeoxyglucose and 18F-florbetapir positron emission tomography scans. In mild cognitive impairment patients, 3 distinct biomarker patterns were recovered, similarly seen in AD patients: (1) in medial temporal regions, local GMV reduction exceeded hypometabolism, (2) in temporoparietal regions, hypometabolism predominated over GMV reduction, and (3) in frontal regions, Aβ deposition exceeded GMV reduction and hypometabolism. In subjective cognitive decline patients, only pattern 1 was detected, while APOE4 carriers demonstrated only pattern 3. Our findings highlight that regional AD-like biomarker patterns may vary across different at-risk populations, potentially reflecting differential mediators of these risks.Entities:
Keywords: Alzheimer's disease; Apolipoprotein E; Mild cognitive impairment; Multimodal neuroimaging; Subjective cognitive decline
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Year: 2017 PMID: 29203090 DOI: 10.1016/j.neurobiolaging.2017.10.023
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673