IN-VIVO CEREBRAL METABOLISM AND CENTRAL BENZODIAZEPINE-RECEPTOR BINDING IN TEMPORAL-LOBE EPILEPSY

被引:158
作者
HENRY, TR
FREY, KA
SACKELLARES, JC
GILMAN, S
KOEPPE, RA
BRUNBERG, JA
ROSS, DA
BERENT, S
YOUNG, AB
KUHL, DE
机构
[1] UNIV MICHIGAN,MED CTR,DEPT NEUROL,N INGALLS BLDG 3D06,400 N INGALLS,ANN ARBOR,MI 48109
[2] UNIV MICHIGAN,MED CTR,DEPT INTERNAL MED,ANN ARBOR,MI 48109
[3] UNIV MICHIGAN,MED CTR,DEPT SURG,ANN ARBOR,MI 48109
[4] UNIV MICHIGAN,MED CTR,DEPT RADIOL,ANN ARBOR,MI 48109
[5] UNIV MICHIGAN,MED CTR,DEPT PSYCHIAT,ANN ARBOR,MI 48109
关键词
D O I
10.1212/WNL.43.10.1998
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Positron emission tomography measured interictal cerebral glucose metabolism with [F-18]fluorodeoxyglucose and central benzodiazepine-receptor binding with [C-11]flumazenil in 10 mesial temporal lobe epilepsy (TLE) patients and in normal subjects. Eight TLE patients had mesial temporal, lateral temporal, and thalamic hypometabolism ipsilateral to EEG ictal onsets, with additional extratemporal hypometabolism in four. One had unilateral anterior mesial temporal hypometabolism only, and one had normal metabolism. Each patient had decreased benzodiazepine-receptor binding in the ipsilateral anterior mesial temporal region, without neocortical changes. Thus, interictal metabolic dysfunction is variable and usually extensive in TLE, whereas decreased central benzodiazepine-receptor density is more restricted to mesial temporal areas. Metabolic patterns in TLE may reflect diaschisis, while benzodiazepine-receptor changes may reflect localized neuronal and synaptic loss that is specific to the epileptogenic zone. [C-11]Flumazenil imaging may be useful in presurgical evaluation of refractory complex partial seizures.
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收藏
页码:1998 / 2006
页数:9
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