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White matter lesions are associated with cortical atrophy more than entorhinal and hippocampal atrophy
An-Tao Du1, Norbert Schuff, Linda L Chao
1Magnetic Resonance Unit (114M), Department of Veterans Affairs Medical Center, 4150, Clement Street, San Francisco, CA 94121, USA.
Abstract:
The goal of this study was to examine the relationship between subcortical vascular disease and brain atrophy in patients with Alzheimer's disease (AD) and mixed dementia (i.e., AD and subcortical vascular disease together). MRI was performed on 77 cognitively normal (CN) subjects, 50 AD and 13 mixed dementia patients. Subcortical vascular disease was determined by white matter hyperintensities (WMH) volume and presence of subcortical lacunes. Brain atrophy was measured using total brain cortical gray matter (CGM), entorhinal cortex (ERC) and hippocampal volumes. CGM volume, but not ERC or hippocampal volume was inversely related to WMH volume in patients and controls. In contrast, no relationship was detected between CGM, ERC, or hippocampal volumes and subcortical lacunes. Furthermore, no interaction was found between WMH and diagnosis on cortical atrophy, implying that WMH affect cortical atrophy indifferently of group. These results suggest that subcortical vascular disease, manifested as WMH, may affect cortical atrophy more than ERC and hippocampal atrophy. Further, AD pathology and subcortical vascular disease may independently affect cortical atrophy.
Insights
White matter hyperintensities (WMH), a marker of subcortical vascular disease, are linked to brain atrophy in Alzheimer's disease (AD) patients. This suggests vascular disease independently impacts cortical atrophy, regardless of AD pathology.
Area of Science:
- Neuroimaging
- Neurology
- Gerontology
Background:
- Alzheimer's disease (AD) is a progressive neurodegenerative disorder.
- Subcortical vascular disease is common in older adults and can coexist with AD.
- The interplay between vascular disease and AD pathology in brain atrophy is not fully understood.
Purpose of the Study:
- To investigate the relationship between subcortical vascular disease and brain atrophy in Alzheimer's disease (AD) and mixed dementia patients.
- To differentiate the effects of white matter hyperintensities (WMH) and lacunes on brain structures.
- To explore whether subcortical vascular disease impacts brain atrophy independently of AD.
Main Methods:
- Magnetic Resonance Imaging (MRI) was used to assess brain structure.
- 77 cognitively normal (CN) subjects, 50 AD patients, and 13 mixed dementia patients were included.
- White matter hyperintensities (WMH) volume and lacunes quantified subcortical vascular disease.
- Cortical gray matter (CGM), entorhinal cortex (ERC), and hippocampal volumes measured brain atrophy.
Main Results:
- Cortical gray matter (CGM) volume showed an inverse relationship with white matter hyperintensities (WMH) volume in all groups.
- No significant relationship was found between brain atrophy measures and subcortical lacunes.
- White matter hyperintensities (WMH) affected cortical atrophy independently of diagnostic group (CN, AD, mixed dementia).
Conclusions:
- Subcortical vascular disease, specifically WMH, is associated with cortical atrophy in individuals with and without Alzheimer's disease.
- White matter hyperintensities (WMH) appear to influence cortical atrophy more than entorhinal cortex or hippocampal atrophy.
- Alzheimer's disease pathology and subcortical vascular disease may contribute independently to cortical atrophy.
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