Hu Chenhui, Hua Xue, Ying Jun, Thompson Paul M, Fakhri Georges E, Li Quanzheng
Microsoft, Cambridge, MA, 02142 USA.
M3 Biotechnology, Seattle, WA, 98195 USA.
IEEE J Sel Top Signal Process. 2016 Oct;10(7):1214-1225. doi: 10.1109/JSTSP.2016.2601695. Epub 2016 Aug 19.
Pinpointing the sources of dementia is crucial to the effective treatment of neurodegenerative diseases. In this paper, we propose a diffusion model with impulsive sources over the brain connectivity network to model the progression of brain atrophy. To reliably estimate the atrophy sources, we impose sparse regularization on the source distribution and solve the inverse problem with an efficient gradient descent method. We localize the possible origins of Alzheimer's disease (AD) based on a large set of repeated magnetic resonance imaging (MRI) scans in Alzheimer's Disease Neuroimaging Initiative (ADNI) database. The distribution of the sources averaged over the sample population is evaluated. We find that the dementia sources have different concentrations in the brain lobes for AD patients and mild cognitive impairment (MCI) subjects, indicating possible switch of the dementia driving mechanism. Moreover, we demonstrate that we can effectively predict changes of brain atrophy patterns with the proposed model. Our work could help understand the dynamics and origin of dementia, as well as monitor the progression of the diseases in an early stage.
确定痴呆症的根源对于神经退行性疾病的有效治疗至关重要。在本文中,我们提出了一种在脑连接网络上具有脉冲源的扩散模型,以模拟脑萎缩的进展。为了可靠地估计萎缩源,我们对源分布施加稀疏正则化,并使用高效的梯度下降方法解决逆问题。我们基于阿尔茨海默病神经影像倡议(ADNI)数据库中的大量重复磁共振成像(MRI)扫描,定位了阿尔茨海默病(AD)的可能起源。评估了样本群体中源的平均分布。我们发现,AD患者和轻度认知障碍(MCI)受试者的痴呆源在脑叶中的浓度不同,这表明痴呆驱动机制可能发生了转变。此外,我们证明了所提出的模型可以有效地预测脑萎缩模式的变化。我们的工作有助于理解痴呆症的动态变化和起源,并在早期监测疾病的进展。