TY - JOUR
T1 - FMRI language dominance and FDG-PET hypometabolism
AU - Gaillard, W. D.
AU - Berl, M. M.
AU - Duke, E. S.
AU - Ritzl, E.
AU - Miranda, S.
AU - Liew, C.
AU - Finegersh, A.
AU - Martinez, A.
AU - Dustin, I.
AU - Sato, S.
AU - Theodore, W. H.
N1 - Funding Information:
Dr. Gaillard has served on a scientific advisory board for GE Healthcare and educational material advisory panels for Ovation Pharmaceuticals (now Lundbeck Inc.) and Questcor Pharmaceuticals, Inc.; served as an editor of Epilepsia ; his department derives income from the clinical evaluation and management of children with epilepsy including performing EEG and vEEG; receives research support from Lundbeck Inc., King Pharmaceuticals, PRA International, Eisai Inc., Marinus Pharmaceuticals, Inc., the NIH (NINDS, NICHD, NIMH), and the CDC; and holds stock in Johnson & Johnson, Eli Lilly and Company, GlaxoSmithKline, and Pfizer Inc. Dr. Berl receives research support from the NIH. E.S. Duke reports no disclosures. Dr. Ritzl's spouse has served on the speakers' bureau for Wyeth. Dr. Miranda, Dr. Liew, A. Finegersh, A. Martinez, and I. Dustin report no disclosures. Dr. Sato receives research support and salary from NIH/NINDS DIR. Dr. Theodore serves as Co-editor-in-Chief of Epilepsy Research ; receives research support and salary from the NIH/NINDS DIR; and holds stock in GE Healthcare.
PY - 2011/4/12
Y1 - 2011/4/12
N2 - Background: Atypical language dominance is common in patients with temporal lobe epilepsy. We examined the association of left temporal hypometabolism with laterality of fMRI activation in a language task in a cross-sectional study. Methods: Thirty patients with temporal lobe epilepsy (mean age 32.4 ± 11.0 years [range 18-55]; epilepsy onset 15.3 ± 11.3 years [range 0.8-40]; 22 left focus, 8 right focus) had fluoro-deoxyglucose (FDG)-PET using noninvasive cardiac input function. After MRI-based partial volume correction, regional glucose metabolism (CMRglc) was measured and asymmetry index, AI = 2(L - R)/(L + R), calculated. fMRI language dominance was assessed with an auditory definition decision paradigm at 3 T. fMRI data were analyzed in SPM2 using regions of interest from Wake Forest PickAtlas (Wernicke area [WA], inferior frontal gyrus [IFG], middle frontal gyrus [MFG]) and bootstrap laterality index, LI = (L - R/L + R). Results: Nineteen patients had ipsilateral temporal hypometabolism; 3 of 4 patients with atypical language had abnormal FDG-PET. Increasing left midtemporal hypometabolism correlated with decreased MFG LI (r = -0.41, p < 0.05) and showed trends with WA LI (r = -0.37, p = 0.055) and IFG LI (r = -0.31, p = 0.099); these relationships became more significant after controlling for age at onset. Increasing hypometabolism was associated with fewer activated voxels in WA ipsilateral to the focus and more activated voxels contralaterally, but overall, activation amount in left WA was similar to subjects without left temporal hypometabolism (t = -1.39, p > 0.10). Conclusions: We did not find evidence of impaired blood oxygenation level-dependent response in hypometabolic cortex. Regional hypometabolism appears to be a marker for the temporal lobe dysfunction that leads to displacement of language function.
AB - Background: Atypical language dominance is common in patients with temporal lobe epilepsy. We examined the association of left temporal hypometabolism with laterality of fMRI activation in a language task in a cross-sectional study. Methods: Thirty patients with temporal lobe epilepsy (mean age 32.4 ± 11.0 years [range 18-55]; epilepsy onset 15.3 ± 11.3 years [range 0.8-40]; 22 left focus, 8 right focus) had fluoro-deoxyglucose (FDG)-PET using noninvasive cardiac input function. After MRI-based partial volume correction, regional glucose metabolism (CMRglc) was measured and asymmetry index, AI = 2(L - R)/(L + R), calculated. fMRI language dominance was assessed with an auditory definition decision paradigm at 3 T. fMRI data were analyzed in SPM2 using regions of interest from Wake Forest PickAtlas (Wernicke area [WA], inferior frontal gyrus [IFG], middle frontal gyrus [MFG]) and bootstrap laterality index, LI = (L - R/L + R). Results: Nineteen patients had ipsilateral temporal hypometabolism; 3 of 4 patients with atypical language had abnormal FDG-PET. Increasing left midtemporal hypometabolism correlated with decreased MFG LI (r = -0.41, p < 0.05) and showed trends with WA LI (r = -0.37, p = 0.055) and IFG LI (r = -0.31, p = 0.099); these relationships became more significant after controlling for age at onset. Increasing hypometabolism was associated with fewer activated voxels in WA ipsilateral to the focus and more activated voxels contralaterally, but overall, activation amount in left WA was similar to subjects without left temporal hypometabolism (t = -1.39, p > 0.10). Conclusions: We did not find evidence of impaired blood oxygenation level-dependent response in hypometabolic cortex. Regional hypometabolism appears to be a marker for the temporal lobe dysfunction that leads to displacement of language function.
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UR - http://www.scopus.com/inward/citedby.url?scp=79954600729&partnerID=8YFLogxK
U2 - 10.1212/WNL.0b013e31821527b5
DO - 10.1212/WNL.0b013e31821527b5
M3 - Article
C2 - 21368285
AN - SCOPUS:79954600729
SN - 0028-3878
VL - 76
SP - 1322
EP - 1329
JO - Neurology
JF - Neurology
IS - 15
ER -