Generalized fused group lasso regularized multi-task feature learning for predicting cognitive outcomes in Alzheimers...

Alzheimers disease (AD) is characterized by gradual neurodegeneration and loss of brain function, especially for memory during early stages. Regression analysis has been widely applied to AD research to relate clinical and biomarker data such as predicting cognitive outcomes from Magnetic Resonance Imaging (MRI) measures. Recently, the multi-task feature learning (MTFL) methods have been widely studied to predict cognitive outcomes and select the discriminative feature subset from MRI features by incorporating inherent correlations among multiple clinical cognitive measures. However, the existing MTFL assumes the correlation among all the tasks is uniform, and the task relatedness is modeled by encouraging a common subset of features with neglecting the inherent structure of tasks and MRI features.

In this paper, we proposed a generalized fused group lasso (GFGL) regularization to model the underlying structures, involving (1) a graph structure within tasks and (2) a group structure among the image features. Then, we present a multi-task learning framework (called GFGL-MTFL), combining the ℓ_{2, 1}-norm with the GFGL regularization, to model the flexible structures.

Through empirical evaluation and comparison with different baseline methods and the state-of-the-art MTL methods on data from Alzheimer's Disease Neuroimaging Initiative (ADNI) database, we illustrate that the proposed GFGL-MTFL method outperforms other methods in terms of both Mean Squared Error (nMSE) and weighted correlation coefficient (wR). Improvements are statistically significant for most scores (tasks).

The experimental results with real and synthetic data demonstrate that incorporating the two prior structures by the generalized fused group lasso norm into the multi task feature learning can improve the prediction performance over several state-of-the-art competing methods, and the estimated correlation of the cognitive functions and the identification of cognition relevant imaging markers are clinically and biologically meaningful.