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Title: Alterations in local cerebral metabolic rates for glucose (LCMRGlc) in childhood epilepsies as determined with FDG and PET

Conference · · J. Nucl. Med.; (United States)
OSTI ID:7032108

The authors investigated LCMRGlc in Lennox-Gastant Syndrome (LGS) (n=15), infantile spasm (IS) (n=14) and Sturge-Weber Syndrome (SWS) (n=5). In children with LGS, 3 distinct metabolic patterns are seen interically: 1) unilateral focal hypometabolism in frontal or temporal lobes, 2) unilateral diffuse hypometabolism, and 3) bilateral diffuse hypometabolism. Therapeutic implications of this classification are: surgical resection in focal (i.e., as for partial epilepsy), corpus callosotomy in diffuse unilateral, and elimination of surgery for those with bilateral diffuse hypometabolism. Babies with idiopathic IS showed symmetrical hypometabolism of lenticular nuclei and midbrain/brain stem compared to cortex and is characterized by slightly better prognosis. In contrast, babies with symtomatic IS had additional CMRGlc disturbances such as bilateral assymetric and multi focal hypometabolism in infant with neurofibromatosis; right parieto-occipital hypometabolims in infant with tuberous sclerosis; intense hypermetabolism of hypothalamus (34.5 vs 3.18 ..mu..moles/-min/100g in other regions) in another where x-ray CT showed only obstructive hydrocephalus. Findings support classical notion of subcortical involvement in this disorder. In SWS, PET showed marked hypometabolism in affected hemisphere in older children, while a 9 month old showed increased LCMRGlc unilaterally (40-50 vs 28-44 ..mu.. moles/min/100g contralateral) with cross cerebellar hypermetabolism (48-50 vs 27-31 ..mu.. moles/min/100g) with no behavioral or EEG evidence of seizure during study. PET studies of LCMRGlc appear sensitive and useful in classifying heterogeneous syndromes into subtypes regarding differential therapy and prognosis, and provide more comprehensive identification of sites of disturbance for investigating mechanisms of these disorders.

Research Organization:
UCLA School of Medicine, Los Angeles, CA
OSTI ID:
7032108
Report Number(s):
CONF-850611-; TRN: 87-010647
Journal Information:
J. Nucl. Med.; (United States), Vol. 26:5; Conference: 32. annual meeting of the Society of Nuclear Medicine, Houston, TX, USA, 2 Jun 1985
Country of Publication:
United States
Language:
English