P. Van Bogaert et al., Statistical parametric mapping of regional glucose metabolism in mesial temporal lobe epilepsy, NEUROIMAGE, 12(2), 2000, pp. 129-138
We investigated statistical parametric mapping (SPM) use for positron emiss
ion tomography (PET) with [F-18]fluorodeoxyglucose (FDG) data analysis in m
esial temporal lobe epilepsy. The study involved 14 patients with temporal
lobe epilepsy ultimately treated by anterior temporal lobectomy. Surgical o
utcome in terms of seizure control was favorable in 12 patients. Two differ
ent SPM approaches were designed to analyze each FDG-PET scan: a direct com
parison with a control group (n = 27) and a search for significant interhem
ispheric asymmetry considering the asymmetry existing in the control group.
Statistical inference was performed, first, without correction for multipl
e comparisons (making the hypothesis of temporal hypometabolism) and, secon
d, after correction for multiple comparisons. Search for temporal interhemi
spheric asymmetry under the hypothesis of temporal hypometabolism was the m
ost reliable SPM approach: hypometabolism was identified on the side chosen
for resection in most cases (sensitivity, 71%; specificity, 100%) and was
predictive of favorable postsurgical outcome in 90% of the patients, There
was no false-positive result within the control group using this approach.
After correction for multiple comparisons, SPM also identified in some pati
ents temporal hypermetabolic areas as well as extratemporal cortical and su
bcortical hypometabolic areas on the side of resection but also on the cont
ralateral side. In a further step, SPM was used for a group analysis of pat
ients with favorable outcome after reversing scans when needed to set an id
entical lateralization in all patients. This analysis identified multiple i
psilateral temporal and extratemporal hypometabolic regions; when temporal
metabolic changes were specifically assessed, the contralateral mesiotempor
al region was found hypermetabolic, possibly as a manifestation of compensa
tory mechanisms in the presence of a unilateral epileptogenic lesion. (C) 2
000 Academic Press.