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Gray matter network differences between behavioral variant frontotemporal dementia and Alzheimer's disease
E G B Vijverberg1, B M Tijms2, J Dopp2
1Alzheimer Centre and Department of Neurology, Amsterdam Neuroscience, VU University Medical Centre, Amsterdam, the Netherlands; Department of Neurology, Haga Ziekenhuis, The Hague, the Netherlands.
Gray matter network disturbances in Alzheimer's disease (AD) and behavioral variant frontotemporal dementia (bvFTD) are distinct and linked to cognitive decline. These findings aid in differentiating neurodegenerative diseases based on brain network alterations.
Area of Science:
- Neuroscience
- Neurology
- Medical Imaging
Background:
- Alzheimer's disease (AD) and behavioral variant frontotemporal dementia (bvFTD) are distinct neurodegenerative conditions.
- Understanding the specific neural network alterations in AD and bvFTD is crucial for accurate diagnosis and treatment.
- Gray matter (GM) network analysis offers a potential method to differentiate these diseases.
Purpose of the Study:
- To investigate if gray matter (GM) network disturbances are specific to Alzheimer's disease (AD) or behavioral variant frontotemporal dementia (bvFTD).
- To determine if these GM network alterations correlate with cognitive deficits.
- To use subjects with subjective cognitive decline as a reference group.
Main Methods:
- Comparative analysis of GM network properties (degree, connectivity density, clustering, path length, betweenness centrality, small world values) between AD, bvFTD, and subjective cognitive decline groups.
- Statistical analysis including ANOVA to compare network metrics between groups.
- Lasso logistic regression to identify specific anatomical areas and network features differentiating AD and bvFTD.
Main Results:
- Both AD and bvFTD patients exhibited lower network metrics (degree, connectivity density, clustering, path length, betweenness centrality, small world values) compared to controls.
- AD patients showed significantly lower connectivity density than bvFTD patients.
- Lasso regression identified 23 anatomical areas with distinct connectivity differences between bvFTD and AD, related to local GM volume, degree, and clustering.
- Lower clustering and degree values were specifically associated with poorer performance on cognitive tests (Mini-Mental State Examination and neuropsychological battery).
Conclusions:
- Gray matter network alterations are disease-specific in Alzheimer's disease and behavioral variant frontotemporal dementia.
- These alterations are significantly associated with the severity of cognitive deficits observed in patients.
- GM network analysis provides valuable insights for differentiating between AD and bvFTD and understanding their impact on cognition.
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