Cd. Ferrie et al., CORTICAL AND SUBCORTICAL GLUCOSE-METABOLISM IN CHILDHOOD EPILEPTIC ENCEPHALOPATHIES, Journal of Neurology, Neurosurgery and Psychiatry, 63(2), 1997, pp. 181-187
Objectives-Nearly one third of children with cryptogenic epileptic enc
ephalopathies have been reported to have focal cortical defects on (18
)fluorodeoxyglucose (FDG) PET. As diffuse cortical dysfunction and inv
olvement of subcortical structures, particularly the thalami, is postu
lated to underlie the propensity to seizures in these conditions, the
aim was to determine the frequency of bilateral and diffuse cortical m
etabolic defects and of subcortical metabolic abnormalities in the sam
e patients. Methods The interictal uptake of FDG was studied in 32 chi
ldren with epileptic encephalopathies. Using a semiquantitative techni
que, the ratio of uptake in cortical regions and subcortical structure
s to that in the cerebellum was compared with that of age matched hist
orical controls. Uptake more than 2 SD above (''hypermetabolic'') or b
elow (''hypometabolic'') that of age matched controls was considered a
bnormal. Results-Diffusely abnormal cortical uptake (nearly always hyp
ometabolic) occurred in almost two thirds of patients; in all but two
of the remaining patients at least one cortical region showed signific
antly decreased uptake bilaterally, When analysed as age cohorts, the
mean cortical:cerebellar FDG uptake was significantly lower than that
of controls in all cortical regions (P < 0.005). Ninety per cent of pa
tients had evidence of relative thalamic hypometabolism and in each ag
e group there was a significant reduction in relative thalamic FDG upt
ake compared with that of controls (P < 0.005). In nine out of 11 pati
ents with unilateral cortical hypometabolic defects thalamic FDG uptak
e was lower ipsilateral to the cortical abnormality. Conclusions-Diffu
se cortical dysfunction is common in the epileptic encephalopathies an
d may reflect the underlying cause of the condition or arise as a cons
equence of uncontrolled seizures. Altered thalamic glucose metabolism
is further evidence of subcortical involvement in these conditions.