Difference in imaging biomarkers of neurodegeneration between early and late-onset amnestic Alzheimer's disease

被引:34
作者
Aziz, Anne-Laure [1 ]
Giusiano, Bernard [1 ,2 ]
Joubert, Sven [3 ,4 ]
Duprat, Laureline [5 ]
Didic, Mira [1 ,6 ,7 ]
Gueriot, Claude [6 ,7 ]
Koric, Lejla [6 ,7 ]
Boucraut, Jose [8 ,9 ]
Felician, Olivier [1 ,6 ,7 ]
Ranjeva, Jean-Philippe [5 ]
Guedj, Eric [10 ,11 ,12 ,13 ]
Ceccaldi, Mathieu [1 ,6 ,7 ]
机构
[1] Aix Marseille Univ, INSERM, UMR 1106, Inst Neurosci Syst, Marseille, France
[2] APHM, Dept Publ Hlth, Marseille, France
[3] Univ Montreal, Dept Psychol, Montreal, PQ, Canada
[4] CRIUGM, Montreal, PQ, Canada
[5] Aix Marseille Univ, CRMBM, CNRS, UMR 7339, Marseille, France
[6] AP HM, Neurol & Neuropyschol Dept, Marseille, France
[7] AP HM, CMRR PACA Ouest, Marseille, France
[8] Assistance Publ Hop Marseille, Immunol & Immunopathol Dept, Marseille, France
[9] Aix Marseille Univ, CRN2M, CNRS, UMR 7286, Marseille 15, France
[10] Timone Hosp, Assistance Publ Hop Marseille, Dept Nucl Med, Marseille, France
[11] Aix Marseille Univ, UMR 7289, Inst Neurosci Timone, Marseille, France
[12] Assistance Publ Hop Marseille, CNRS, Marseille, France
[13] Aix Marseille Univ, CERIMED, Marseille, France
关键词
Alzheimer's disease; Age of onset; Neuroimaging biomarkers; Magnetic resonance imaging; Positron emission tomography imaging; COGNITIVE DECLINE; MCI PATIENTS; MEMORY; AGE; DEMENTIA; PATTERNS; REHABILITATION; ASSOCIATION; ATROPHY;
D O I
10.1016/j.neurobiolaging.2017.02.010
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
030301 [社会学]; 100201 [内科学];
摘要
Neuroimaging biomarkers differ between patients with early-onset Alzheimer's disease (EOAD) and lateonset 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. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:22 / 30
页数:9
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