Functional imaging in late-onset epilepsy: A focused review
Isha Puntambekar1, Fenglai Xiao1, Robert Shortman2
1Department of Clinical and experimental Epilepsy, UCL Queen Square Institute of Neurology, Queen Square, London, UK; Epilepsy Society, Chalfont St. Peter, Buckinghamshire, UK.
Late-onset epilepsy (LOE) diagnosis in older adults is a growing concern. While FDG-PET and amyloid PET show promise, current research lacks standardized methods for definitive conclusions.
Area of Science:
- Neurology
- Neuroimaging
- Geriatrics
Background:
- Late-onset epilepsy (LOE) affects 25% of new-onset epilepsy cases in individuals over 65.
- LOE is projected to increase due to global population aging, posing a significant healthcare challenge.
- Neurodegenerative disorders are implicated in 10-20% of LOE cases, with over 20% having unknown causes.
Purpose of the Study:
- To review the utility of functional neuroimaging techniques in diagnosing late-onset epilepsy.
- To assess the potential of FDG-PET and novel biomarkers like amyloid and tau PET in identifying neurodegenerative causes of LOE.
Main Methods:
- A literature search was performed to identify studies utilizing functional neuroimaging in late-onset epilepsy populations.
- Boolean searching and snowballing techniques were employed to gather relevant articles.
Main Results:
- Five studies met the inclusion criteria.
- Significant heterogeneity was observed across studies regarding LOE definitions, analytical methods, and interpretation pipelines.
Conclusions:
- Preliminary evidence suggests FDG-PET and amyloid PET are feasible for LOE diagnosis.
- Methodological inconsistencies in current literature prevent definitive conclusions.
- Standardized guidelines for epilepsy-specific analysis and interpretation of amyloid and tau PET are needed for future research.
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