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Different patterns of white matter disruption among amnestic mild cognitive impairment subtypes: relationship with
He Li1, Ying Liang, Kewei Chen
1State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, Beijing, PR China.
Abstract:
Amnestic mild cognitive impairment (aMCI) is recognized as the prodromal phase of Alzheimer's disease (AD). Evidence showed that patients with multiple-domain (MD) aMCI were at higher risk of converting to dementia and exhibited more severe gray matter atrophy than single-domain (SD) aMCI. The investigation of the microstructural abnormalities of white matter (WM) among different subtypes of aMCI and their relations with cognitive performances can help to understand the variations among aMCI subtypes and to construct potential imaging based biomarkers to monitor the progression of aMCI. Diffusion-weighted MRI data were acquired from 40 patients with aMCI (aMCI-SD: n = 19; aMCI-MD: n = 21) and 37 healthy controls (HC). Voxel-wise and atlas-based analyses of whole-brain WM were performed among three groups. The correlations between the altered diffusion metrics of the WM tracts and the neuropsychological scores in each subtype of aMCI were assessed. The aMCI-MD patients showed disrupted integrity in multiple WM tracts across the whole-brain when compared with HCs or with aMCI-SD. In contrast, only few WM regions with diffusion changes were found in aMCI-SD as compared to HCs and with less significance. For neuropsychological correlations, only aMCI-MD patients exhibited significant associations between disrupted WM connectivity (in the body of the corpus callosum and the right anterior internal capsules) and cognitive impairments (MMSE and Digit Symb-Coding scores), whereas no such correlations were found in aMCI-SD. These findings indicate that the degeneration extensively exists in WM tracts in aMCI-MD that precedes the development of AD, whereas underlying WM pathology in aMCI-SD is imperceptible. The results are consistent with the view that aMCI is not a uniform disease entity and presents heterogeneity in the clinical progression.
Insights
Multiple-domain amnestic mild cognitive impairment (aMCI-MD) shows widespread white matter (WM) damage linked to cognitive decline. Single-domain aMCI (aMCI-SD) exhibits minimal WM changes, suggesting distinct disease progression pathways.
Area of Science:
- Neuroimaging
- Neurology
- Alzheimer's Disease Research
Background:
- Amnestic mild cognitive impairment (aMCI) is a precursor to Alzheimer's disease (AD).
- Multiple-domain aMCI (aMCI-MD) carries a higher risk of dementia progression and shows greater gray matter loss than single-domain aMCI (aMCI-SD).
- Understanding white matter (WM) microstructural changes in aMCI subtypes is crucial for identifying biomarkers and monitoring disease progression.
Purpose of the Study:
- To investigate white matter (WM) microstructural abnormalities in aMCI subtypes (aMCI-MD vs. aMCI-SD) using diffusion-weighted MRI.
- To explore the relationship between altered WM integrity and cognitive performance in each aMCI subtype.
- To differentiate the pathological profiles of aMCI-MD and aMCI-SD.
Main Methods:
- Diffusion-weighted MRI data analyzed using voxel-wise and atlas-based approaches in 40 aMCI patients (19 aMCI-SD, 21 aMCI-MD) and 37 healthy controls (HC).
- Comparison of WM diffusion metrics across the three groups.
- Correlation analysis between diffusion metrics and neuropsychological scores (MMSE, Digit Symb-Coding) within aMCI subtypes.
Main Results:
- aMCI-MD patients exhibited significantly disrupted WM integrity in multiple tracts compared to HC and aMCI-SD.
- aMCI-SD showed only minor WM diffusion changes compared to HC.
- Significant correlations between WM connectivity deficits (corpus callosum, anterior internal capsules) and cognitive impairments were observed exclusively in aMCI-MD.
Conclusions:
- WM degeneration is extensive in aMCI-MD, preceding Alzheimer's disease development.
- WM pathology in aMCI-SD appears minimal or undetectable with current methods.
- aMCI is a heterogeneous condition, not a uniform disease entity, with distinct progression patterns based on domain involvement.
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