Nomi Jason S, Bolt Taylor S, Ezie C E Chiemeka, Uddin Lucina Q, Heller Aaron S
Department of Psychology, University of Miami, Coral Gables, Florida 33124, and
Department of Psychology, University of Miami, Coral Gables, Florida 33124, and.
J Neurosci. 2017 May 31;37(22):5539-5548. doi: 10.1523/JNEUROSCI.3408-16.2017. Epub 2017 May 4.
Variability of neuronal responses is thought to underlie flexible and optimal brain function. Because previous work investigating BOLD signal variability has been conducted within task-based fMRI contexts on adults and older individuals, very little is currently known regarding regional changes in spontaneous BOLD signal variability in the human brain across the lifespan. The current study used resting-state fMRI data from a large sample of male and female human participants covering a wide age range (6-85 years) across two different fMRI acquisition parameters (TR = 0.645 and 1.4 s). Variability in brain regions including a key node of the salience network (anterior insula) increased linearly across the lifespan across datasets. In contrast, variability in most other large-scale networks decreased linearly over the lifespan. These results demonstrate unique lifespan trajectories of BOLD variability related to specific regions of the brain and add to a growing literature demonstrating the importance of identifying normative trajectories of functional brain maturation. Although brain signal variability has traditionally been considered a source of unwanted noise, recent work demonstrates that variability in brain signals during task performance is related to brain maturation in old age as well as individual differences in behavioral performance. The current results demonstrate that intrinsic fluctuations in resting-state variability exhibit unique maturation trajectories in specific brain regions and systems, particularly those supporting salience detection. These results have implications for investigations of brain development and aging, as well as interpretations of brain function underlying behavioral changes across the lifespan.
神经元反应的变异性被认为是灵活且最佳大脑功能的基础。由于先前关于血氧水平依赖(BOLD)信号变异性的研究是在基于任务的功能磁共振成像(fMRI)环境中对成年人和年长者进行的,目前对于人类大脑在整个生命周期中自发BOLD信号变异性的区域变化知之甚少。本研究使用了来自大量男性和女性人类参与者的静息态fMRI数据,这些参与者年龄范围广泛(6 - 85岁),涉及两种不同的fMRI采集参数(重复时间TR = 0.645秒和1.4秒)。包括突显网络的一个关键节点(前脑岛)在内的脑区变异性在整个生命周期中随数据集呈线性增加。相比之下,大多数其他大规模网络的变异性在整个生命周期中呈线性下降。这些结果表明了与大脑特定区域相关的BOLD变异性独特的生命周期轨迹,并为越来越多证明识别功能性脑成熟规范轨迹重要性的文献增添了内容。尽管传统上脑信号变异性被认为是不需要的噪声来源,但最近的研究表明,任务执行期间脑信号的变异性与老年脑成熟以及行为表现的个体差异有关。当前结果表明,静息态变异性的内在波动在特定脑区和系统中呈现出独特的成熟轨迹,特别是那些支持突显检测的区域。这些结果对脑发育和衰老的研究以及对整个生命周期中行为变化背后脑功能的解释具有启示意义。