GPU Accelerated Modeling of Cortical Radial and Tangential Connectivity Changes in Neurodegeneration.

Hongbo Zhang, Xinyu Nie, Jiaxin Yue, Yuan Li, John Ringman, Yonggang Shi
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Abstract

The diffusion MRI signals in the human cerebral cortex are strongly associated with neurodegenerative diseases. Although models like NODDI have been extensively used to characterize cortical microstructure degeneration, they fall short in capturing detailed, orientation-specific connectivity changes within the cortex. In this study, we introduce a method to decompose cortical tissue diffusion signal to radial and tangential components. Our approach uses data from multi-shell diffusion imaging and combines it with anatomical information from brain surfaces. By applying a GPU accelerated probabilistic optimization framework, we can accurately and efficiently estimate these diffusion components while keeping the results smooth and consistent with the cortical anatomy. We test our method on data from HCP subjects and a clinical dataset of patients with autosomal dominant Alzheimer's Disease (ADAD) subjects. Our results demonstrate that the proposed method can more effectively reveal cortical gray matter connectivity changes related to tau pathology than metrics from the NODDI model. Our codebase is publicly available at https://github.com/Haibaobob/FOD-ctx-decomp.

GPU加速建模神经退行性变性皮质径向和切向连通性变化。
人类大脑皮层弥散性MRI信号与神经退行性疾病密切相关。尽管像NODDI这样的模型已被广泛用于表征皮层微观结构的退化,但它们在捕捉皮层内详细的定向特异性连接变化方面存在不足。在本研究中,我们介绍了一种将皮质组织扩散信号分解为径向和切向分量的方法。我们的方法使用来自多壳扩散成像的数据,并将其与大脑表面的解剖信息相结合。通过应用GPU加速概率优化框架,我们可以准确有效地估计这些扩散分量,同时保持结果的平滑性和与皮质解剖结构的一致性。我们在HCP患者和常染色体显性阿尔茨海默病(ADAD)患者的临床数据集上测试了我们的方法。我们的研究结果表明,与NODDI模型的指标相比,该方法可以更有效地揭示与tau病理相关的皮层灰质连接变化。我们的代码库可以在https://github.com/Haibaobob/FOD-ctx-decomp上公开获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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