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Brain Structural Changes and Cognitive-Clinical Profiles in Late-Onset Unexplained Epilepsy.
Ariane Kek-Laflamme1, Frederic L W V J Schaper2, Kevin Whittingstall3
1Department of Pharmacology-Physiology, Faculty of Medicine and Health Sciences, Université de Sherbrooke, QC, Canada.
Late-onset unexplained epilepsy (LOUE) involves widespread brain changes, including reduced cortical thickness and deep gray matter volumes. These alterations are linked to cognitive deficits, suggesting a potential continuum with neurodegenerative diseases.
Area of Science:
- Neurology
- Neuroimaging
- Cognitive Neuroscience
Background:
- Epilepsy incidence is bimodal, with a second peak after age 55.
- Late-onset unexplained epilepsy (LOUE) often lacks identifiable causes, with prior imaging suggesting mesiotemporal atrophy.
- Understanding structural brain alterations in LOUE is crucial for diagnosis and management.
Purpose of the Study:
- To quantify whole-brain cortical and deep gray matter alterations in LOUE.
- To investigate the association between these structural changes and cognitive/clinical measures in LOUE patients.
Main Methods:
- Prospective recruitment of LOUE patients and comparison with healthy older adults.
- Utilized 3T structural MRI to extract cortical thickness and deep gray matter volumes.
- Employed linear models for group comparisons and correlation analyses with cognitive and clinical data.
Main Results:
- LOUE patients exhibited reduced cortical thickness in sensory/mesiotemporal regions and decreased pallidum/putamen volumes.
- Structural reductions correlated with poorer performance on fluency and memory tasks.
- Increased thickness in the inferior frontal gyrus and thalamic volume were observed, particularly in patients with focal seizures.
Conclusions:
- LOUE is associated with more extensive brain structural changes than previously understood.
- These changes are linked to cognitive vulnerabilities, indicating potential overlap with neurodegenerative processes.
- Findings suggest LOUE may represent a spectrum between epilepsy and neurodegeneration.
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