Yuan Xinrui, Cheng Jiale, Hu Dan, Wu Zhengwang, Wang Li, Lin Weili, Li Gang
Department of Radiology and Biomedical Research Imaging Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
bioRxiv. 2024 Dec 20:2024.12.19.629222. doi: 10.1101/2024.12.19.629222.
Brain functional connectivity patterns exhibit distinctive, individualized characteristics capable of distinguishing one individual from others, like fingerprint. Accurate and reliable depiction of individualized functional connectivity patterns during infancy is crucial for advancing our understanding of individual uniqueness and variability of the intrinsic functional architecture during dynamic early brain development, as well as its role in neurodevelopmental disorders. However, the highly dynamic and rapidly developing nature of the infant brain presents significant challenges in capturing robust and stable functional fingerprint, resulting in low accuracy in individual identification over ages during infancy using functional connectivity. Conventional methods rely on brain parcellations for computing inter-regional functional connections, which are sensitive to the chosen parcellation scheme and completely ignore important fine-grained, spatially detailed patterns in functional connectivity that encodes developmentally-invariant, subject-specific features critical for functional fingerprinting. To solve these issues, for the first time, we propose a novel method to leverage the high-resolution, vertex-level local gradient map of functional connectivity from resting-state functional MRI, which captures sharp changes and subject-specific rich information of functional connectivity patterns, to explore infant functional fingerprint. Leveraging a longitudinal dataset comprising 591 high-resolution resting-state functional MRI scans from 103 infants, our method demonstrates superior performance in infant individual identification across ages. Our method has unprecedentedly achieved 99% individual identification rates across three age-varied sub-datasets, with consistent and robust identification rates across different phase encoding directions, significantly outperforming atlas-based approaches with only around 70% accuracy. Further vertex-wise uniqueness and differential power analyses highlighted the discriminative identifiability of higher-order functional networks. Additionally, the local gradient-based functional fingerprints demonstrated reliable predictive capabilities for cognitive performance during infancy. These findings suggest the existence of unique individualized functional fingerprints during infancy and underscore the potential of local gradients of functional connectivity in capturing neurobiologically meaningful and fine-grained features of individualized characteristics for advancing normal and abnormal early brain development.
脑功能连接模式呈现出独特的、个性化的特征,能够像指纹一样将一个人与其他人区分开来。准确可靠地描绘婴儿期的个性化功能连接模式,对于增进我们对动态早期脑发育过程中内在功能结构的个体独特性和变异性,以及其在神经发育障碍中的作用的理解至关重要。然而,婴儿脑的高度动态和快速发育的特性,在捕捉稳健和稳定的功能指纹方面带来了重大挑战,导致在婴儿期使用功能连接进行跨年龄个体识别的准确性较低。传统方法依赖于脑图谱来计算区域间的功能连接,这对所选的图谱方案敏感,并且完全忽略了功能连接中重要的细粒度、空间详细模式,这些模式编码了对功能指纹识别至关重要的发育不变的、个体特异性特征。为了解决这些问题,我们首次提出了一种新颖的方法,利用静息态功能磁共振成像的高分辨率、顶点级局部梯度图,该图捕捉了功能连接模式的急剧变化和个体特异性丰富信息,以探索婴儿功能指纹。利用包含来自103名婴儿的591次高分辨率静息态功能磁共振成像扫描的纵向数据集,我们的方法在跨年龄的婴儿个体识别中表现出卓越的性能。我们的方法在三个年龄各异的子数据集中前所未有的实现了99%的个体识别率,在不同相位编码方向上具有一致且稳健的识别率,显著优于基于图谱的方法,后者的准确率仅约为70%。进一步的顶点特异性唯一性和差异功率分析突出了高阶功能网络的鉴别可识别性。此外,基于局部梯度的功能指纹显示出对婴儿期认知表现的可靠预测能力。这些发现表明婴儿期存在独特的个性化功能指纹,并强调了功能连接局部梯度在捕捉神经生物学上有意义的和细粒度的个体特征以推进正常和异常早期脑发育方面的潜力。