Functional neuroanatomical associations of working memory in early-onset Alzheimer's disease

被引:8
|
作者
Kobylecki, Christopher [1 ,2 ]
Haense, Cathleen [1 ,3 ]
Harris, Jennifer M. [1 ,2 ]
Stopford, Cheryl L. [1 ,2 ]
Segobin, Shailendra H. [1 ,4 ]
Jones, Matthew [1 ,2 ]
Richardson, Anna M. T. [1 ,5 ]
Gerhard, Alexander [1 ,2 ]
Anton-Rodriguez, Jose [1 ]
Thompson, Jennifer C. [1 ,2 ]
Herholz, Karl [1 ]
Snowden, Julie S. [1 ,2 ]
机构
[1] Univ Manchester, Sch Biol Sci, Div Neurosci & Expt Psychol, Fac Biol Med & Hlth, Manchester, Lancs, England
[2] Salford Royal NHS Fdn Trust, Cerebral Funct Unit, Greater Manchester Neurosci Ctr, Salford, Lancs, England
[3] Hannover Med Sch, Dept Nucl Med, Hannover, Germany
[4] Univ Caen Basse Normandie, EPHE, INSERM, Caen, France
[5] Univ Manchester, Manchester Med Sch, Manchester, Lancs, England
关键词
Alzheimer's disease; FDG-PET; working memory; neuropsychology; APOE GENOTYPE; APOLIPOPROTEIN-E; DIAGNOSIS; PRESENTATIONS; PERFORMANCE; DEMENTIA; DEFICITS; NETWORK; BRAIN; HRRT;
D O I
10.1002/gps.4703
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
ObjectiveTo characterize metabolic correlates of working memory impairment in clinically defined subtypes of early-onset Alzheimer's disease. BackgroundEstablished models of working memory suggest a key role for frontal lobe function, yet the association in Alzheimer's disease between working memory impairment and visuospatial and language symptoms suggests that temporoparietal neocortical dysfunction may be responsible. MethodsTwenty-four patients with predominantly early-onset Alzheimer's disease were clinically classified into groups with predominantly amnestic, multidomain or visual deficits. Patients underwent neuropsychological evaluation focused on the domains of episodic and working memory, T1-weighted magnetic resonance imaging and brain fluorodeoxyglucose positron emission tomography. Fluorodeoxyglucose positron emission tomography data were analysed by using a region-of-interest approach. ResultsPatients with multidomain and visual presentations performed more poorly on tests of working memory compared with amnestic Alzheimer's disease. Working memory performance correlated with glucose metabolism in left-sided temporoparietal, but not frontal neocortex. Carriers of the apolipoprotein E4 gene showed poorer episodic memory and better working memory performance compared with noncarriers. ConclusionsOur findings support the hypothesis that working memory changes in early-onset Alzheimer's disease are related to temporoparietal rather than frontal hypometabolism and show dissociation from episodic memory performance. They further support the concept of subtypes of Alzheimer's disease with distinct cognitive profiles due to prominent neocortical dysfunction early in the disease course. Copyright (c) 2017 John Wiley & Sons, Ltd.
引用
收藏
页码:176 / 184
页数:9
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