Yang Fan, Roy Chowdhury Samadrita, Jacobs Heidi I L, Johnson Keith A, Dutta Joyita
Department of Electrical and Computer Engineering, University of Massachusetts Lowell, Lowell, MA, USA.
Massachusetts General Hospital & Harvard Medical School, Boston, MA, USA
Inf Process Med Imaging. 2019;11492:384-393. doi: 10.1007/978-3-030-20351-1_29. Epub 2019 May 22.
Tau tangles are a pathological hallmark of Alzheimer?s disease (AD) with strong correlations existing between tau aggregation and cognitive decline. Studies in mouse models have shown that the characteristic patterns of tau spatial spread associated with AD progression are determined by neural connectivity rather than physical proximity between different brain regions. We present here a network diffusion model for tau aggregation based on longitudinal tau measures from positron emission tomography (PET) and structural connectivity graphs from diffusion tensor imaging (DTI). White matter fiber bundles reconstructed via tractography from the DTI data were used to compute normalized graph Laplacians which served as graph diffusion kernels for tau spread. By linearizing this model and using sparse source localization, we were able to identify distinct patterns of propagative and generative buildup of tau at a population level. A gradient descent approach was used to solve the sparsity-constrained optimization problem. Model fitting was performed on subjects from the Harvard Aging Brain Study cohort. The fitted model parameters include a scalar factor controlling the network-based tau spread and a network-independent seed vector representing seeding in different regions-of-interest. This parametric model was validated on an independent group of subjects from the same cohort. We were able to predict with reasonably high accuracy the tau buildup at a future time-point. The network diffusion model, therefore, successfully identifies two distinct mechanisms for tau buildup in the aging brain and offers a macroscopic perspective on tau spread.
tau缠结是阿尔茨海默病(AD)的一个病理标志,tau聚集与认知衰退之间存在着很强的相关性。对小鼠模型的研究表明,与AD进展相关的tau空间扩散特征模式是由神经连接性决定的,而非不同脑区之间的物理距离。我们在此提出一种基于正电子发射断层扫描(PET)的纵向tau测量值和扩散张量成像(DTI)的结构连接图的tau聚集网络扩散模型。通过对DTI数据进行纤维束成像重建的白质纤维束被用于计算归一化图拉普拉斯算子,其作为tau扩散的图扩散核。通过线性化该模型并使用稀疏源定位,我们能够在群体水平上识别tau传播性和生成性积累的不同模式。采用梯度下降法来解决稀疏约束优化问题。对来自哈佛衰老大脑研究队列的受试者进行模型拟合。拟合的模型参数包括一个控制基于网络的tau扩散的标量因子和一个代表不同感兴趣区域中种子点的与网络无关的种子向量。该参数模型在来自同一队列的独立受试者组上得到验证。我们能够以相当高的准确率预测未来某个时间点的tau积累情况。因此,该网络扩散模型成功识别了衰老大脑中tau积累的两种不同机制,并为tau扩散提供了一个宏观视角。