INTERICTAL REGIONAL SLOW ACTIVITY IN TEMPORAL-LOBE EPILEPSY CORRELATES WITH LATERAL TEMPORAL HYPOMETABOLISM AS IMAGED WITH (18)FDG PET - NEUROPHYSIOLOGICAL AND METABOLIC IMPLICATIONS
M. Koutroumanidis et al., INTERICTAL REGIONAL SLOW ACTIVITY IN TEMPORAL-LOBE EPILEPSY CORRELATES WITH LATERAL TEMPORAL HYPOMETABOLISM AS IMAGED WITH (18)FDG PET - NEUROPHYSIOLOGICAL AND METABOLIC IMPLICATIONS, Journal of Neurology, Neurosurgery and Psychiatry, 65(2), 1998, pp. 170-176
Objectives-The phenomenon of interictal regional slow activity (IRSA)
in temporal lobe epilepsy and its relation with cerebral glucose metab
olism, clinical data, MRT, and histopathological findings was studied.
Methods-Interictal F-18-fluorodeoxyglucose positron emission tomograp
hy (FDG PET) was performed under continuous scalp EEG monitoring in 28
patients with temporal lobe epilepsy not associated with intracranial
foreign tissue lesions, all of whom subsequently underwent resective
surgery. Regions of interest (ROIs) were drawn according to a standard
template. IRSA was considered lateralised when showing a 4:1 or great
er ratio of predominance on one side. Results-Sixteen patients (57%) h
ad lateralised IRSA which was always ipsilateral to the resection and
of maximal amplitude over the temporal areas. Its presence was signifi
cantly related to the presence of hypometabolism in the lateral tempor
al neocortex (p=0.0009). Logistic regression of the asymmetry indices
for all measured cerebral regions confirmed a strong association betwe
en IRSA and decreased metabolism of the posterior lateral temporal neo
cortex only (p=0.009). No significant relation could be shown between
slow activity and age at onset, duration of the epilepsy, seizure freq
uency, and MRI evidence for hippocampal atrophy. Furthermore, IRSA was
not specifically related to mesial temporal sclerosis or any other pa
thology. Conclusions-Interictal regional slowing in patients with temp
oral lobe epilepsy not associated with a mass lesion is topographicall
y related to the epileptogenic area and therefore has a reliable later
alising, and possibly localising, value. Its presence is irrelevant to
the severity or chronicity of the epilepsy as well as to lateral deac
tivation secondary to neuronal loss in the mesial temporal structures.
Although slow EEG activity is generally considered as a non-specific
sign of functional disturbance, interictal regional slowing in tempora
l lobe epilepsy should be conceptualised as a distinct electrographic
phenomenon which is directly related to the epileptogenic abnormality.
The strong correlation between interictal regional slowing and latera
l temporal hypometabolism suggests in turn that the second may delinea
te a field of reduced neuronal inhibition which can receive interictal
and ictal propagation.