Department of Psychiatry, Veterans Affairs San Diego Healthcare System, School of Medicine, University of California, San Diego, CA 92161, USA.
Neuroimage. 2010 Jul 1;51(3):1222-33. doi: 10.1016/j.neuroimage.2010.03.021. Epub 2010 Mar 16.
Recent language studies in aging and dementia provide two complementary lines of evidence that: (1) measures of semantic knowledge and word-finding ability show declines comparable to those of episodic memory, and greater impairment than executive function measures, during the prodromal period of Alzheimer's disease and (2) cognitively intact older adult carriers of the apolipoprotein E (APOE) epsilon4 allele also demonstrate poorer object naming than their low-risk peers. Given that possible changes in the neural substrates of word retrieval (e.g., Broca's area and fusiform gyrus) in at-risk adults may signal impending cognitive decline and serve as a prodromal marker of AD, we examined whether APOE epsilon4 carriers exhibit changes in brain response in regions subserving word retrieval and semantic knowledge. Eleven cognitively intact APOE epsilon4 older adults and 11 age, education, and family history of AD-matched APOE epsilon3 adults named aloud photographs of animals, tools, and vehicles during event-related fMRI. Results showed that, in the face of equivalent naming accuracy, APOE epsilon4 adults demonstrated more widespread brain response with greater signal change in the left fusiform gyrus, bilateral medial prefrontal cortex, and right perisylvian cortex. Findings are discussed in the context of possible compensatory mechanisms invoked to maintain performance in those at genetic risk for AD.
(1)在阿尔茨海默病的前驱期,语义知识和寻词能力的测量与情景记忆的下降相当,比执行功能测量的下降更为严重;(2)载脂蛋白 E(APOE)ε4 等位基因的认知正常的老年成年人也表现出比低风险同龄人更差的物体命名能力。鉴于高危成年人单词检索的神经基础(例如,布洛卡区和梭状回)可能发生变化,这可能预示着认知能力下降,并作为 AD 的前驱标志物,我们研究了 APOE ε4 携带者是否在单词检索和语义知识的大脑反应区域中表现出变化。11 名认知正常的 APOE ε4 老年人和 11 名年龄、教育程度和 AD 家族史匹配的 APOE ε3 成年人在事件相关 fMRI 期间大声说出动物、工具和车辆的照片。结果表明,面对相同的命名准确性,APOE ε4 成年人在左侧梭状回、双侧内侧前额叶皮层和右侧周围大脑皮层中表现出更广泛的大脑反应,信号变化更大。研究结果在可能的补偿机制的背景下进行了讨论,这些机制被用来维持那些有 AD 遗传风险的人的表现。