Literature DB >> 8304838

Asymmetric interictal glucose hypometabolism and cognitive performance in epileptic patients.

R Rausch1, T R Henry, C M Ary, J Engel, J Mazziotta.   

Abstract

OBJECTIVE: To relate hemispheric metabolic asymmetries to cognitive performance in patients with unilateral mesial temporal lobe epilepsy.
DESIGN: Asymmetrical cerebral glucose metabolisms on interictal fludeoxyglucose F 18 positron emission tomograms (FDG-PET) were correlated with cognitive measures. Analyses included partial correlations that controlled for the correlation between metabolic asymmetries of the lateral temporal lobe and other brain regions and the correlation of IQ scores with affected cognitive scores.
SETTING: A university epilepsy surgery center. PATIENTS: Subjects included 13 patients who had intractable complex partial seizures originating from a mesial temporal lobe. INTERVENTION: Patients underwent FDG-PET scanning as part of their diagnostic work-up. Asymmetry indexes for cerebral metabolic rates were determined for whole hemisphere, lateral temporal lobe, mesial temporal lobe, frontal lobe, thalamus, and parietal lobe. MAIN OUTCOME MEASURES: The following cognitive domains were assessed: psychometric intelligence, mental control/attention, language, and verbal and nonverbal memory. Neuropsychological measures were obtained within 14 days of FDG-PET scanning.
RESULTS: Relative reductions in glucose metabolism of the left hemisphere and left lateral temporal lobe correlated with a lower verbal IQ score and a lower score on a verbal memory task, recall of logical prose. Relative reduction in metabolism of the left side of the thalamus also correlated with lower scores for recall of logical prose.
CONCLUSION: Relative hypometabolism of the left hemisphere correlates with lower cognitive performance. Hypometabolism of the left lateral temporal lobe and thalamus independently correlates with the verbal memory difficulties seen in this epileptic patient population.

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Year:  1994        PMID: 8304838     DOI: 10.1001/archneur.1994.00540140045013

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


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