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Neurocognitive Profile and 18 F-Fluorodeoxyglucose Positron Emission Tomography Brain Imaging Correlation in Children
Madhur K Srivastava1, Afshan J Shaik2, Sireesha Yareeda2
1Department of Nuclear Medicine, Nizam's Institute of Medical Sciences (NIMS), Panjagutta, Hyderabad, Telangana, India.
Insights
Electrical status epilepticus in sleep (ESES) in children is linked to cognitive and behavioral issues, with brain scans showing reduced metabolism in key areas. The extent of these brain changes correlates with the severity of neuropsychological deficits and epilepsy duration.
Area of Science:
- Neuroscience
- Pediatric Neurology
- Medical Imaging
Background:
- Electrical status epilepticus in sleep (ESES) is characterized by continuous epileptiform discharges during sleep.
- ESES is associated with cognitive, behavioral, and neuroimaging abnormalities.
- Understanding the neurocognitive profile and brain metabolism in ESES is crucial for diagnosis and management.
Purpose of the Study:
- To investigate the neurocognitive profile of children with ESES.
- To correlate neurocognitive deficits with brain abnormalities detected by 18F-fluorodeoxyglucose positron emission tomography (FDG PET).
- To compare FDG PET findings in ESES patients with a control group.
Main Methods:
- Studied 14 children with ESES and normal MRI.
- Assessed intelligence quotient (IQ) and Child Behavior Checklist (CBCL) scores.
- Performed FDG PET scans to identify cerebral metabolic defects.
Main Results:
- Children with ESES showed lower average IQ and higher CBCL scores.
- Negative correlation found between IQ and CBCL scores, and between epilepsy duration and IQ.
- FDG PET revealed predominant thalamic hypometabolism in 85.7% of patients, with other cortical and subcortical abnormalities.
- Significant differences in basal ganglia metabolism compared to controls.
- Extent of hypometabolism correlated with CBCL scores but not IQ.
Conclusions:
- ESES patients exhibit functional brain impairment with hypometabolism in cortical, basal ganglia, and thalamic regions, even with normal structural MRI.
- The degree of cerebral hypometabolism correlates with neuropsychological status and epilepsy duration.
- FDG PET is a valuable tool for assessing functional brain changes in ESES.
Abstract:
Objective Electrical status epilepticus in sleep (ESES) is defined by near-continuous epileptiform discharges during sleep along with cognitive, behavioral, and/or imaging abnormalities. We studied the neurocognitive profile and their correlation with 18 F fluorodeoxyglucose positron emission tomography (FDG PET) brain abnormalities in children with ESES. Methods Fourteen children with ESES with normal magnetic resonance imaging (MRI) from March to December 2019 were included. The intelligence quotient (IQ) and child behavior checklist (CBCL) scores were estimated using validated scales, and FDG PET brain was done at the same point of time to look for cerebral metabolic defects which was compared with a control group. Results Fourteen patients with a mean age of 8.2 ± 2.7 years were analyzed. The average duration of epilepsy was 6 ± 2.8 years. The mean IQ was 72.4 ± 18.2 and mean CBCL score was 37.3 ± 11.8. There was negative correlation between IQ and CBCL ( r = -0.55, p < 0.001). The duration of epilepsy also showed negative correlation with IQ ( r = -4.75, p < 0.001). FDG PET scan showed predominant thalamic hypometabolism in 12 of 14 patients (85.7%) on visual analysis with multiple other hypometabolic cortical and subcortical regions in the brain. The quantitative analysis showed significant difference in metabolism of basal ganglion when compared with control group. The total number of hypometabolic regions seen in the brain showed moderate positive correlation with CBCL score but no significant correlation with the IQ of cases. Conclusion This study demonstrates functional impairment of cerebral cortical, basal ganglia, and thalamic hypometabolism in a cohort of ESES patients with normal structural MRI brain study. There was a moderate correlation of extent and pattern of cerebral hypometabolism with the neuropsychological status of the child and duration of epilepsy.
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