Department of Psychology, Centre for Lifespan Changes in Brain and Cognition, University of Oslo, Oslo 0317, Norway.
Umeå Centre for Functional Brain Imaging, S-90187 Umeå, Sweden.
Cereb Cortex. 2021 Mar 5;31(4):2098-2110. doi: 10.1093/cercor/bhaa348.
It has been suggested that specific forms of cognition in older age rely largely on late-life specific mechanisms. Here instead, we tested using task-fMRI (n = 540, age 6-82 years) whether the functional foundations of successful episodic memory encoding adhere to a principle of lifespan continuity, shaped by developmental, structural, and evolutionary influences. We clustered regions of the cerebral cortex according to the shape of the lifespan trajectory of memory activity in each region so that regions showing the same pattern were clustered together. The results revealed that lifespan trajectories of memory encoding function showed a continuity through life but no evidence of age-specific mechanisms such as compensatory patterns. Encoding activity was related to general cognitive abilities and variations of grey matter as captured by a multi-modal independent component analysis, variables reflecting core aspects of cognitive and structural change throughout the lifespan. Furthermore, memory encoding activity aligned to fundamental aspects of brain organization, such as large-scale connectivity and evolutionary cortical expansion gradients. Altogether, we provide novel support for a perspective on memory aging in which maintenance and decay of episodic memory in older age needs to be understood from a comprehensive life-long perspective rather than as a late-life phenomenon only.
有人认为,老年人的特定认知形式在很大程度上依赖于特定于晚年的机制。在这里,我们使用任务 fMRI(n=540,年龄 6-82 岁)来测试,成功的情景记忆编码的功能基础是否遵循一个贯穿生命的连续性原则,该原则受到发育、结构和进化的影响。我们根据每个区域记忆活动的寿命轨迹的形状对大脑皮层区域进行聚类,以便将表现出相同模式的区域聚类在一起。结果表明,记忆编码功能的寿命轨迹在整个生命周期中保持连续性,但没有证据表明存在特定于年龄的机制,如补偿模式。编码活动与一般认知能力和多模态独立成分分析捕获的灰质变化有关,这些变量反映了认知和结构变化的核心方面,贯穿整个生命周期。此外,记忆编码活动与大脑组织的基本方面相一致,如大规模连接和进化皮层扩展梯度。总的来说,我们为记忆老化的观点提供了新的支持,即从全面的终身角度理解老年人情景记忆的维持和衰退,而不仅仅是晚年现象。