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Group Guided Fused Laplacian Sparse Group Lasso for Modeling Alzheimer’s Disease Progression

机译:集团导游融合拉普拉斯稀疏集团套索模拟阿尔茨海默病进展

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As the largest cause of dementia, Alzheimer’s disease (AD) has brought serious burdens to patients and their families, mostly in the financial, psychological, and emotional aspects. In order to assess the progression of AD and develop new treatment methods for the disease, it is essential to infer the trajectories of patients’ cognitive performance over time to identify biomarkers that connect the patterns of brain atrophy and AD progression. In this article, a structured regularized regression approach termed group guided fused Laplacian sparse group Lasso (GFL-SGL) is proposed to infer disease progression by considering multiple prediction of the same cognitive scores at different time points (longitudinal analysis). The proposed GFL-SGL simultaneously exploits the interrelated structures within the MRI features and among the tasks with sparse group Lasso (SGL) norm and presents a novel group guided fused Laplacian (GFL) regularization. This combination effectively incorporates both the relatedness among multiple longitudinal time points with a general weighted (undirected) dependency graphs and useful inherent group structure in features. Furthermore, an alternating direction method of multipliers- (ADMM-) based algorithm is also derived to optimize the nonsmooth objective function of the proposed approach. Experiments on the dataset from Alzheimer’s Disease Neuroimaging Initiative (ADNI) show that the proposed GFL-SGL outperformed some other state-of-the-art algorithms and effectively fused the multimodality data. The compact sets of cognition-relevant imaging biomarkers identified by our approach are consistent with the results of clinical studies.
机译:作为痴呆症最大的原因,阿尔茨海默病(AD)对患者及其家属带来了严重的负担,主要是在金融,心理和情感方面。为了评估广告的进展并对疾病进行新的治疗方法,必须推断患者认知性能随时间的轨迹,以鉴定连接脑萎缩和广告进展模式的生物标志物。在本文中,提出了一种由基团引导的融合拉普拉斯稀疏组套索(GFL-SGL)的结构化正规回归方法通过考虑在不同时间点(纵向分析)的同一认知分数的多次预测来推断疾病进展。所提出的GFL-SGL同时利用MRI功能内的相互关联的结构以及具有稀疏组卢斯(SGL)规范的任务,并提出了一种新颖的组导向融合拉普拉斯(GFL)正规化。该组合有效地结合了多个纵向时间点之间的相关性,其具有一般加权(无向)依赖图和特征中的有用固有组结构。此外,还导出了基于乘法器的交替方向方法,以优化所提出的方法的非光滑目标函数。来自阿尔茨海默病的DataSet的实验神经影像倡议(ADNI)表明,所提出的GFL-SGL优于一些最先进的算法,并有效地融合了多模数据数据。我们方法鉴定的紧凑型认知相关成像生物标志物与临床研究的结果一致。

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