Abstract

The Alzheimer’s Disease Assessment Scale-Cognitive subscale (ADAS-Cog) is a neuropsychological tool that has been designed to assess the severity of cognitive symptoms of dementia. Personalized prediction of the changes in ADAS-Cog scores could help in timing therapeutic interventions in dementia and at-risk populations. In the present work, we compared single and multitask learning approaches to predict the changes in ADAS-Cog scores based on T1-weighted anatomical magnetic resonance imaging (MRI). In contrast to most machine learning-based prediction methods ADAS-Cog changes, we stratified the subjects based on their baseline diagnoses and evaluated the prediction performances in each group. Our experiments indicated a positive relationship between the predicted and observed ADAS-Cog score changes in each diagnostic group, suggesting that T1-weighted MRI has a predictive value for evaluating cognitive decline in the entire AD continuum. We further studied whether correction of the differences in the magnetic field strength of MRI would improve the ADAS-Cog score prediction. The partial least square-based domain adaptation slightly improved the prediction performance, but the improvement was marginal. In summary, this study demonstrated that ADAS-Cog change could be, to some extent, predicted based on anatomical MRI. Based on this study, the recommended method for learning the predictive models is a single-task regularized linear regression due to its simplicity and good performance. It appears important to combine the training data across all subject groups for the most effective predictive models.

Highlights

  • Alzheimer’s Disease (AD) is a chronic neurodegenerative disorder that occurs mainly among the elderly, and 152 million people are expected to suffer from AD in 2050 [1]

  • To correct for differences in features caused by imaging at two magnetic field strengths (MFS) in ADNI1 and ADNI2, we studied three different techniques: 1) partial least squares (PLS)-based domain adaptation introduced in [34], 2) ComBat harmonization originating from genetics [35], which has become widely used in brain imaging [42], [54], and 3) multi-task learning

  • These scatter plots imply that the ∆ ADAS-Cog scores with very high values for all time-points were the hardest to predict since the number of individuals with observed ADAS-Cog score change over 20 was small (e.g.., The number of Mild cognitive impairment (MCI) subjects at 12, 24, and 36 months were 2, 8, and 19, respectively)

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Summary

Introduction

Alzheimer’s Disease (AD) is a chronic neurodegenerative disorder that occurs mainly among the elderly, and 152 million people are expected to suffer from AD in 2050 [1]. Pathophysiological changes of AD begin many years prior to clinical manifestations of disease and the spectrum of AD spans from clinically asymptomatic to severely impaired [2]. There is an appreciation that AD should be viewed with discrete and defined clinical stages but as a multifaceted process moving along a continuum. Mild cognitive impairment (MCI) is an important concept along this continuum, representing a transitional stage between healthy elderly and AD [3]. 10% to 20% of MCI patients tend to progress to AD annually, whereas others will continue with cognitive decline or even revert to normal control (NC) [4].

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