Abstract

Introduction: Alzheimer’s disease (AD) is a neurodegenerative disorder with a clinical presentation characterized by memory impairment and executive dysfunction. Our group previously demonstrated significant alterations in white matter microstructural metrics in AD compared to healthy older adults. We aimed to further investigate the relationship between white matter microstructure in AD and cognitive function, including memory and executive function.Methods: Diffusion tensor imaging (DTI) and neuropsychological data were downloaded from the AD Neuroimaging Initiative database for 49 individuals with AD and 48 matched healthy older adults. The relationship between whole-brain fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AxD), radial diffusivity (RD), and composite scores of memory and executive function was examined. We also considered voxel-wise relationships using Tract-Based Spatial Statistics.Results: As expected, individuals with AD had lower composite scores on tests of memory and executive function, as well as disrupted white matter integrity (low FA, high MD, AxD, and RD) relative to healthy older adults in widespread regions, including the hippocampus. When the AD and healthy older adult groups were combined, we found significant relationships between DTI metrics (FA/MD/AxD/RD) and memory scores across widespread regions of the brain, including the medial temporal regions. We also found significant relationships between DTI metrics (FA/MD/AxD/RD) and executive function in widespread regions, including the frontal areas in the combined group. However, when the groups were examined separately, no significant relationships were found between DTI metrics (FA/MD/AxD/RD) and memory performance for either group. Further, we did not find any significant relationships between DTI metrics (FA/MD/AxD/RD) and executive function in the AD group, but we did observe significant relationships between FA/RD, and executive function in healthy older adults.Conclusion: White matter integrity is disrupted in AD. In a mixed sample of AD and healthy elderly persons, associations between measures of white matter microstructure and memory and executive cognitive test performance were evident. However, no significant linear relationship between the degree of white matter disruption and level of cognitive functioning (memory and executive abilities) was found in those with AD. Future longitudinal studies of the relations between DTI metrics and cognitive function in AD are required to determine whether DTI has potential to measure progression of AD and/or treatment efficacy.

Highlights

  • Alzheimer’s disease (AD) is a neurodegenerative disorder with a clinical presentation characterized by memory impairment and executive dysfunction

  • We found lower fractional anisotropy (FA) and higher mean diffusivity (MD), axial diffusivity (AxD), and radial diffusivity (RD) in the AD group compared to healthy older adults across widespread regions, including the hippocampal regions, as has been previously reported (Mayo et al, 2017)

  • When we examined the groups separately, we did not find any significant relationships between diffusion tensor imaging (DTI) metrics and memory test composite scores (ADNI-MEM) within either the AD or healthy older adult groups

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Summary

Introduction

Alzheimer’s disease (AD) is a neurodegenerative disorder with a clinical presentation characterized by memory impairment and executive dysfunction. We aimed to further investigate the relationship between white matter microstructure in AD and cognitive function, including memory and executive function. AD is a neurodegenerative disorder typically characterized by memory loss, other cognitive domains, including executive functions, are often affected as well (Kirova et al, 2015; Alzheimer’s Association, 2017). The majority of MRI research on AD has focused on neurodegeneration in gray matter structures (Teipel et al, 2013; Cash et al, 2014). These findings indicate widespread, whole brain atrophy in individuals with AD, including enlarged ventricles and decreased hippocampal volume (Perl, 2010; Hampel et al, 2014). There is less research on white matter, which is affected early in the disease process (Sachdev et al, 2013), and the relationship between white matter integrity and cognitive function in AD

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