Effects of Aging on Recollection, Familiarity, and Conceptual Priming

衰老对记忆、熟悉度和概念启动的影响

• 批准号: 8251249
• 负责人: Ilana T. Z. Dew
• 金额: $ 5.29万
• 依托单位: DUKE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-09-24 至 2013-09-23
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8251249
• 关键词: Accounting; Aging; Alzheimer' s Disease; Behavioral; Biological Preservation; Brain; Brain region; Cognitive; Cognitive aging; Concept Formation; Conscious; Diffusion Magnetic Resonance Imaging; Dissociation; Elderly; Episodic memory; Event; Exposure to; Familiarity; Feeling; Fiber; Functional Magnetic Resonance Imaging; Functional disorder; Goals; Hippocampus (Brain); Image Analysis; Individual Differences; Inferior; Judgment; Left; Link; Measures; Mediating; Memory; Memory impairment; Pathway interactions; Patients; Performance; Play; Prefrontal Cortex; Research; Retrieval; Role; Signal Transduction; Site; Source; Task Performances; Testing; age effect; age related; base; cognitive neuroscience; cognitive rehabilitation; cognitive training; healthy aging; implicit memory; improved; interest; lexical processing; memory process; neuropathology; neuropsychological; pathological aging; public health relevance; relating to nervous system; semantic processing; white matter; young adult

DESCRIPTION (provided by applicant): A major goal in cognitive neuroscience of aging is to identify the neural bases of cognitive abilities that are impaired vs. spared by aging. Recollection is the form of memory most impaired by healthy aging and Alzheimer's Disease. Recollection refers to vividly remembering a past event including its associated contextual details, and it differs from familiarity, which refers to the vague feeling that the event occurred in the past even though details cannot be retrieved. Behavioral studies have provided strong evidence that older adults are impaired in recollection but largely unimpaired in familiarity (for a review, see Yonelinas, 2002). Very little is known about the neural bases of this dissociation. In young adults, recollection has been shown to be more dependent on the hippocampus and prefrontal cortex (PFC), while familiarity is more dependent on the rhinal cortex. However, it is unclear whether age-related declines in recollection are primarily mediated by hippocampal or PFC dysfunction. Furthermore, it is uncertain whether the sparing of familiarity is related to the preservation of conceptual priming, a form of implicit memory in which memory performance is facilitated by previous exposure to semantically-related information. The proposed study integrates three methodological approaches to investigate the scope and limits of impaired and preserved episodic memory processes in older adults. First, functional magnetic resonance imaging (fMRI) is used to determine whether older and younger adults use similar or different brain regions during recollection, familiarity, and conceptual priming. Second, diffusion tensor imaging (DTI) is used to quantify white matter integrity in pathways linking regions of interest. Finally, a test battery is used to assess individual differences in neuropsychological status (NS) and determine whether varying levels of executive and memory function can account for differences in task performance and in associated brain activity. These three approaches will be used together to investigate each question of interest. The proposed project is significant for several reasons. Although PFC dysfunction is assumed to play a major role in cognitive aging, the contribution of this region to memory deficits in older adults is still uncertain. In addition, the rhinal cortex is one of the first sites of Alzheimer's Disease neuropathology; thus, understanding its precise role in memory is an important step in distinguishing healthy aging from pathological aging. Moreover, if we can show that the reengagement of conceptual information during measures of familiarity is used to influence and improve memory judgments, then this offers a potential avenue for cognitive training and rehabilitation. Thus, investigating these questions is important at both basic and applied levels. PUBLIC HEALTH RELEVANCE: The rhinal cortex is one of the first sites of Alzheimer's Disease neuropathology; thus, understanding its precise role in memory is an important step in distinguishing healthy aging from pathological aging. Moreover, if we can show that the reengagement of conceptual information during measures of familiarity is used to influence and improve memory judgments, then this offers a potential avenue for cognitive training and rehabilitation. Thus, investigating these questions is important at both basic and applied levels.

描述（由申请人提供）：衰老认知神经科学的一个主要目标是确定因衰老而受损或保留的认知能力的神经基础。回忆是最受健康衰老和阿尔茨海默病损害的记忆形式。“回忆”指的是对过去发生的事情的记忆，包括相关的背景细节。“回忆”与“熟悉”不同，“熟悉”指的是对过去发生的事情的模糊感觉，即使无法回忆细节。行为学研究提供了强有力的证据，表明老年人在回忆方面受损，但在熟悉度方面基本没有受损（回顾，见Yonelinas， 2002）。我们对这种分离的神经基础知之甚少。在年轻人中，回忆更依赖于海马体和前额皮质（PFC），而熟悉更依赖于鼻皮质。然而，尚不清楚与年龄相关的记忆力下降是否主要由海马或PFC功能障碍介导。此外，尚不确定熟悉度的保留是否与概念启动的保存有关，概念启动是一种内隐记忆形式，其中记忆表现通过先前接触语义相关信息而促进。该研究整合了三种方法来研究老年人情景记忆过程受损和保留的范围和限制。首先，使用功能性磁共振成像（fMRI）来确定老年人和年轻人在回忆、熟悉和概念启动时使用的大脑区域是相似还是不同。其次，扩散张量成像（DTI）用于量化连接感兴趣区域的通路中的白质完整性。最后，一个测试单元被用来评估神经心理状态（NS）的个体差异，并确定不同水平的执行和记忆功能是否可以解释任务表现和相关大脑活动的差异。这三种方法将一起用于调查每个感兴趣的问题。拟议中的项目之所以重要，有几个原因。尽管PFC功能障碍被认为在认知衰老中起主要作用，但该区域在老年人记忆缺陷中的作用仍不确定。此外，鼻皮层是阿尔茨海默病神经病理学的第一个部位之一；因此，了解其在记忆中的确切作用是区分健康衰老和病理性衰老的重要一步。此外，如果我们能够证明在熟悉度测量过程中概念性信息的再参与被用来影响和改善记忆判断，那么这就为认知训练和康复提供了一条潜在的途径。因此，研究这些问题在基础和应用层面都很重要。