Abstract

BackgroundThe human brain is complex and interconnected structurally. Brain connectome change is associated with Alzheimer’s disease (AD) and other neurodegenerative diseases. Genetics and genomics studies have identified molecular changes in AD; however, the results are often limited to isolated brain regions and are difficult to interpret its findings in respect to brain connectome. The mechanisms of how one brain region impacts the molecular pathways in other regions have not been systematically studied. And how the brain regions susceptible to AD pathology interact with each other at the transcriptome level and how these interactions relate to brain connectome change are unclear.MethodsHere, we compared structural brain connectomes defined by probabilistic tracts using diffusion magnetic resonance imaging data in Alzheimer’s Disease Neuroimaging Initiative database and a brain transcriptome dataset covering 17 brain regions.ResultsWe observed that the changes in diffusion measures associated with AD diagnosis status and the associations were replicated in an independent cohort. The result suggests that disease associated white matter changes are focal. Analysis of the brain connectome by genomic data, tissue-tissue transcriptional synchronization between 17 brain regions, indicates that the regions connected by AD-associated tracts were likely connected at the transcriptome level with high number of tissue-to-tissue correlated (TTC) gene pairs (P = 0.03). And genes involved in TTC gene pairs between white matter tract connected brain regions were enriched in signaling pathways (P = 6.08 × 10−9). Further pathway interaction analysis identified ionotropic glutamate receptor pathway and Toll receptor signaling pathways to be important for tissue-tissue synchronization at the transcriptome level. Transcript profile entailing Toll receptor signaling in the blood was significantly associated with diffusion properties of white matter tracts, notable association between fractional anisotropy and bilateral cingulum angular bundles (Ppermutation = 1.0 × 10−2 and 4.9 × 10−4 for left and right respectively).ConclusionsIn summary, our study suggests that brain connectomes defined by MRI and transcriptome data overlap with each other.

Highlights

  • The human brain is complex and interconnected structurally

  • The primary goal of Alzheimer’s Disease Neuroimaging Initiative (ADNI) has been to test whether serial magnetic resonance imaging (MRI), positron emission tomography (PET), other biological markers, and clinical and neuropsychological assessment can be combined to measure the progression of mild cognitive impairment (MCI) and early Alzheimer’s disease (AD)

  • radial diffusivity (RD) was more significantly correlated with volume than mean diffusivity (MD)

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Summary

Introduction

The human brain is complex and interconnected structurally. Brain connectome change is associated with Alzheimer’s disease (AD) and other neurodegenerative diseases. Much of the human brain connectome has been assessed using magnetic resonance imaging (MRI) where functional MRI and diffusion MRI (dMRI) can measure correlated neural activity and structural connectivity of the brain in vivo, respectively [1, 2]. Various neurological diseases such as Alzheimer’s disease (AD) are associated with disruption of the brain connectome and studies show that the course of AD continuum is associated with the changes in brain network architecture [3,4,5]. The mechanisms of how one brain region impacts molecular pathways in other regions, especially how the brain regions susceptible to AD pathology interact with each other at the transcriptome level, have not been systematically studied

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