Division of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
Cerebral Function Unit, Greater Manchester Neurosciences Centre, Salford Royal NHS Foundation Trust, Salford, UK.
Int J Geriatr Psychiatry. 2018 Jan;33(1):176-184. doi: 10.1002/gps.4703. Epub 2017 Mar 16.
To characterize metabolic correlates of working memory impairment in clinically defined subtypes of early-onset Alzheimer's disease.
Established 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.
Twenty-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.
Patients 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.
Our 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 © 2017 John Wiley & Sons, Ltd.
描述早期发病阿尔茨海默病临床定义亚型中工作记忆损伤的代谢相关性。
已建立的工作记忆模型提示额叶功能起关键作用,但阿尔茨海默病中工作记忆损伤与视空间和语言症状的关联表明颞顶叶新皮质功能障碍可能是其原因。
24 例以早期发病阿尔茨海默病为主的患者通过临床分类归入以单纯记忆障碍、多领域障碍或视觉障碍为主的组。患者接受了以情景记忆和工作记忆为重点的神经心理学评估、T1 加权磁共振成像和脑氟脱氧葡萄糖正电子发射断层扫描。采用感兴趣区分析法分析氟脱氧葡萄糖正电子发射断层扫描数据。
与单纯记忆障碍型阿尔茨海默病患者相比,多领域和视觉表现型患者在工作记忆测试中表现更差。工作记忆表现与左侧颞顶叶而不是额叶新皮质的葡萄糖代谢相关。载脂蛋白 E4 基因携带者的情景记忆比非携带者差,但工作记忆表现更好。
我们的研究结果支持这样的假设,即早期发病阿尔茨海默病中的工作记忆改变与颞顶叶而非额叶代谢降低有关,且与情景记忆表现分离。它们进一步支持了由于疾病早期突出的皮质功能障碍而具有不同认知特征的阿尔茨海默病亚型的概念。