Center for Translational Research in Neuroimaging and Data Science (TReNDS): Georgia State University, Georgia Institute of Technology, and Emory University, Atlanta, USA; Department of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, USA.
Center for Translational Research in Neuroimaging and Data Science (TReNDS): Georgia State University, Georgia Institute of Technology, and Emory University, Atlanta, USA.
J Neurosci Methods. 2024 Jun;406:110109. doi: 10.1016/j.jneumeth.2024.110109. Epub 2024 Mar 15.
For successful biomarker discovery, it is essential to develop computational frameworks that summarize high-dimensional neuroimaging data in terms of involved sub-systems of the brain, while also revealing underlying heterogeneous functional and structural changes covarying with specific cognitive and biological traits. However, unsupervised decompositions do not inculcate clinical assessment information, while supervised approaches extract only individual feature importance, thereby impeding qualitative interpretation at the level of subspaces.
We present a novel framework to extract robust multimodal brain subspaces associated with changes in a given cognitive or biological trait. Our approach involves active subspace learning on the gradients of a trained machine learning model followed by clustering to extract and summarize the most salient and consistent subspaces associated with the target variable.
Through a rigorous cross-validation procedure on an Alzheimer's disease (AD) dataset, our framework successfully extracts multimodal subspaces specific to a given clinical assessment (e.g., memory and other cognitive skills), and also retains predictive performance in standard machine learning algorithms. We also show that the salient active subspace directions occur consistently across randomly sub-sampled repetitions of the analysis.
COMPARISON WITH EXISTING METHOD(S): Compared to existing unsupervised decompositions based on principle component analysis, the subspace components in our framework retain higher predictive information.
As an important step towards biomarker discovery, our framework not only uncovers AD-related brain regions in the associated brain subspaces, but also enables automated identification of multiple underlying structural and functional sub-systems of the brain that collectively characterize changes in memory and proficiency in cognitive skills related to brain disorders like AD.
为了成功发现生物标志物,开发能够根据大脑相关子系统总结高维神经影像学数据的计算框架是至关重要的,同时还需要揭示与特定认知和生物学特征相关的潜在异质功能和结构变化。然而,无监督分解没有包含临床评估信息,而监督方法仅提取单个特征的重要性,从而阻碍了子空间层面的定性解释。
我们提出了一种新的框架,用于提取与给定认知或生物学特征变化相关的稳健多模态大脑子空间。我们的方法涉及在训练后的机器学习模型的梯度上进行主动子空间学习,然后进行聚类以提取和总结与目标变量最相关和一致的子空间。
通过对阿尔茨海默病 (AD) 数据集进行严格的交叉验证程序,我们的框架成功地提取了特定于给定临床评估的多模态子空间(例如,记忆和其他认知技能),并且在标准机器学习算法中保留了预测性能。我们还表明,突出的主动子空间方向在分析的随机子采样重复中一致出现。
与基于主成分分析的现有无监督分解方法相比,我们框架中的子空间成分保留了更高的预测信息。
作为生物标志物发现的重要步骤,我们的框架不仅揭示了相关脑子空间中的 AD 相关脑区,而且还能够自动识别多个潜在的结构和功能子系统,这些子系统共同描述了与 AD 等大脑障碍相关的记忆和认知技能熟练程度的变化。