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Published on: January 11, 2020
Cognitive impairment in early onset epilepsy is associated with reduced left thalamic volume
Michael Yoong1, Matthew Hunter2, Jacqueline Stephen3
1Muir Maxwell Epilepsy Centre, University of Edinburgh, UK; Department of Paediatric Neurology, Royal Hospital for Sick Children, Edinburgh, UK.
Insights
Reduced left thalamic volume in children with early onset epilepsy (CWEOE) is linked to cognitive impairment. This finding may serve as a biomarker for early detection and intervention in affected children.
Area of Science:
- Neuroscience
- Pediatric Neurology
- Medical Imaging
Background:
- Early onset epilepsy (onset <5 years) can impact cognitive development in children.
- Thalamic volume abnormalities have been suggested as a potential indicator of neurological dysfunction.
Purpose of the Study:
- To investigate the association between reduced thalamic volumes and cognitive impairment in children with early onset epilepsy (CWEOE).
Main Methods:
- A nested case-control study involving 76 children with newly-diagnosed early onset epilepsy and 14 healthy controls.
- Quantitative volumetric analysis of subcortical structures using T1-weighted MRI.
- Correlation of thalamic volumes with formal neurocognitive and clinical assessments, with statistical significance determined by false discovery rate (q<0.05).
Main Results:
- Children with early onset epilepsy and cognitive impairment exhibited significantly reduced left thalamic volumes compared to those without impairment and healthy controls (q<0.001).
- These volume differences persisted when adjusting for gray matter or cortical/cerebellar volumes.
- The extent of left thalamic volume reduction correlated with the severity of cognitive impairment (q=0.048).
Conclusions:
- Reduced left thalamic volume may serve as a potential biomarker for cognitive impairment in children with early onset epilepsy.
- Identifying this biomarker could aid in informing the need for cognitive evaluations and interventions in this population.
Objective:
The objective of this study was to investigate whether reduction of thalamic volumes in children with early onset epilepsy (CWEOE) is associated with cognitive impairment.
Methods:
This is a nested case-control study including a prospectively recruited cohort of 76 children with newly-diagnosed early onset epilepsy (onset <5years age) and 14 healthy controls presenting to hospitals within NHS Lothian and Fife. Quantitative volumetric analysis of subcortical structures was performed using volumetric T1-weighted magnetic resonance imaging (MRI) and correlated with the results of formal neurocognitive and clinical assessment. False discovery rate was used to correct for multiple comparisons as appropriate with q<0.05 used to define statistical significance.
Results:
Age, gender, and intracranial volume (ICV)-adjusted left thalamic volumes were significantly reduced in CWEOE with cognitive impairment compared to CWEOE without impairment (5295mm3 vs 6418mm3, q=0.008) or healthy controls (5295mm3 vs 6410mm3, q<0.001). The differences in left thalamic volume remained if gray matter or cortical/cerebellar volumes were used as covariates rather than ICV (q<0.05). The degree of volume reduction correlated with the severity of cognitive impairment (q=0.048).
Significance:
Reduced left thalamic volume may be a biomarker for cognitive impairment in CWEOE and could help inform the need for further formal cognitive evaluations and interventions.
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