Abstract

Mild cognitive impairment (MCI) represents a transitional stage from normal aging to Alzheimer’s disease (AD) and corresponds to a higher risk of developing AD. Thus, it is necessary to explore and predict the onset of AD in MCI stage. In this study, we propose a combination of independent component analysis (ICA) and the multivariate Cox proportional hazards regression model to investigate promising risk factors associated with MCI conversion among 126 MCI converters and 108 MCI non-converters from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database. Using structural magnetic resonance imaging (MRI) and fluorodeoxyglucose positron emission tomography (FDG-PET) data, we extracted brain networks from AD and normal control groups via ICA and then constructed Cox models that included network-based neuroimaging factors for the MCI group. We carried out five separate Cox analyses and the two-modality neuroimaging Cox model identified three significant network-based risk factors with higher prediction performance (accuracy = 73.50%) than those in either single-modality model (accuracy = 68.80%). Additionally, the results of the comprehensive Cox model, including significant neuroimaging factors and clinical variables, demonstrated that MCI individuals with reduced gray matter volume in a temporal lobe-related network of structural MRI [hazard ratio (HR) = 8.29E-05 (95% confidence interval (CI), 5.10E- 07 ~ 0.013)], low glucose metabolism in the posterior default mode network based on FDG-PET [HR = 0.066 (95% CI, 4.63E-03 ~ 0.928)], positive apolipoprotein E ε4-status [HR = 1. 988 (95% CI, 1.531 ~ 2.581)], increased Alzheimer’s Disease Assessment Scale-Cognitive Subscale scores [HR = 1.100 (95% CI, 1.059 ~ 1.144)] and Sum of Boxes of Clinical Dementia Rating scores [HR = 1.622 (95% CI, 1.364 ~ 1.930)] were more likely to convert to AD within 36 months after baselines. These significant risk factors in such comprehensive Cox model had the best prediction ability (accuracy = 84.62%, sensitivity = 86.51%, specificity = 82.41%) compared to either neuroimaging factors or clinical variables alone. These results suggested that a combination of ICA and Cox model analyses could be used successfully in survival analysis and provide a network-based perspective of MCI progression or AD-related studies.

Highlights

  • Alzheimer’s disease (AD) is one of the most severe neurodegenerative diseases and is accompanied by structural and functional changes in the brain (Brookmeyer et al, 2007; Dartigues, 2009; Jack et al, 2010a; Reitz et al, 2011; Prince, 2015)

  • We found that reduced gray matter volume in structural magnetic resonance imaging (MRI) images, low glucose metabolism according to fluorodeoxyglucose positron emission tomography (FDG-PET), increased ADAS-cog scores and Clinical Dementia Rating (CDR)-SB scores, and a positive apolipoprotein E (APOE) ε4-status had significant effects on the progression of Mild cognitive impairment (MCI) to AD

  • Our study incorporated different models and populations compared with Prestia et al (2013), our findings suggested that biomarkers of FDG-PET or structural MRI could be used in predicting MCI conversion

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Summary

INTRODUCTION

Alzheimer’s disease (AD) is one of the most severe neurodegenerative diseases and is accompanied by structural and functional changes in the brain (Brookmeyer et al, 2007; Dartigues, 2009; Jack et al, 2010a; Reitz et al, 2011; Prince, 2015). By considering imaging data to be linear combinations of statistically independent sources, ICA has been widely used to investigate brain structural or functional networks in different populations (Beckmann et al, 2005; Mantini et al, 2007; Segall et al, 2012; Hafkemeijer et al, 2014). The voxels within such networks carry similar covariate information (Xu et al, 2009). Multivariate Cox proportional hazards regression models consisting of different types of covariates among MCI individuals were constructed

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