Abstract

Relating disease status to imaging data stands to increase the clinical significance of neuroimaging studies. Many neurological and psychiatric disorders involve complex, systems-level alterations that manifest in functional and structural properties of the brain and possibly other clinical and biologic measures. We propose a Bayesian hierarchical model to predict disease status, which is able to incorporate information from both functional and structural brain imaging scans. We consider a two-stage whole brain parcellation, partitioning the brain into 282 subregions, and our model accounts for correlations between voxels from different brain regions defined by the parcellations. Our approach models the imaging data and uses posterior predictive probabilities to perform prediction. The estimates of our model parameters are based on samples drawn from the joint posterior distribution using Markov Chain Monte Carlo (MCMC) methods. We evaluate our method by examining the prediction accuracy rates based on leave-one-out cross validation, and we employ an importance sampling strategy to reduce the computation time. We conduct both whole-brain and voxel-level prediction and identify the brain regions that are highly associated with the disease based on the voxel-level prediction results. We apply our model to multimodal brain imaging data from a study of Parkinson's disease. We achieve extremely high accuracy, in general, and our model identifies key regions contributing to accurate prediction including caudate, putamen, and fusiform gyrus as well as several sensory system regions.

Highlights

  • Functional and structural neuroimaging play important roles in understanding the neurological basis for major psychiatric and neurological disorders such as Parkinson’s disease (PD), schizophrenia, depression, and Alzheimer’s diseases

  • There have been reports of cortical cortical thinning in PD patients determined from T1-MRI scans (Lee et al, 2013; Zarei et al, 2013; Zhang et al, 2015), decreased fractional anisotropy in the substantia nigra revealed by diffusion tensor imaging (DTI) (Vaillancourt et al, 2009), and functional connectivity, structural connectivity, and volumetric PD-related changes revealed by a multimodal imaging analysis (Bowman et al, 2016)

  • We applied our proposed Bayesian spatial model to PD data, which has T1 and resting-state functional magnetic resonance imaging (fMRI) images available; our model reduces to one which includes two imaging modalities, voxel based morphometry (VBM) and fractional amplitude of low-frequency fluctuation (fALFF), and only considers data in the gray matter

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Summary

Introduction

Functional and structural neuroimaging play important roles in understanding the neurological basis for major psychiatric and neurological disorders such as Parkinson’s disease (PD), schizophrenia, depression, and Alzheimer’s diseases. There have been reports of cortical cortical thinning in PD patients determined from T1-MRI scans (Lee et al, 2013; Zarei et al, 2013; Zhang et al, 2015), decreased fractional anisotropy in the substantia nigra revealed by diffusion tensor imaging (DTI) (Vaillancourt et al, 2009), and functional connectivity, structural connectivity, and volumetric PD-related changes revealed by a multimodal imaging analysis (Bowman et al, 2016) These and other related studies suggest the utility of imaging data in revealing neuropathophysiology related the loss of dopamine producing neurons in PD and prompt the need for new methods to accommodate high-dimensional multimodal data

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