You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 54 No. 2, February 1997 TABLE OF CONTENTS
  Archives
  •  Online Features
  ARTICLE
 This Article
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal

Pattern of interictal hypometabolism in PET scans with fludeoxyglucose F 18 reflects prior seizure types in patients with mesial temporal lobe seizures

I. Savic, L. Altshuler, L. Baxter and J. Engel Jr
Department of Neurology, UCLA School of Medicine, USA.

BACKGROUND: Interictal hypometabolism is routinely used as an indicator of the epileptogenic zone in patients with complex partial seizures (CPSs). However, the regional pattern of hypometabolism varies without obvious reasons, even among patients with identical epileptogenic zones and causes. OBJECTIVE: To investigate whether this pattern may be related to the electroencephalographic and clinical features of the seizure that precedes the positron emission tomographic (PET) scan with fludeoxyglucose F 18. PATIENTS AND METHODS: Fifty-three patients with CPSs were first classified into 4 groups, depending on the features of the seizure that preceded the PET scan (determined from findings from electroencephalography and videotelemetry). In 14 patients, this seizure was focal limbic (characterized by aurae or staring spells); in 18, the CPS was widespread limbic (including automatisms). Ten patients had a CPS with posturing, and 11 had a secondarily generalized CPS. Regions with a hemisphere-normalized concentration of fludeoxyglucose F 18 below the 95% confidence interval of values from 8 control subjects were defined as hypometabolic. The location of these regions was then compared among the 4 groups, and the degree of hypometabolism was related to the time from the seizure to the PET scan with fludeoxyglucose F 18. RESULTS: The hypometabolic area was limited to the epileptogenic zone if the preceding seizure was focal limbic, whereas in patients with widespread limbic seizures, it included one or several additional areas of the limbic cortex (P = .03). Patients with posturing differed from both previous groups by having hypometabolism in the extralimbic frontal lobe (P < .001), and subjects with secondarily generalized seizures differed from all others because of cerebellar (P < .001) and parietal lobe (P < .05) reductions. The time between the seizure and the performance of the PET scan did not correlate with the degree or extent of hypometabolism. CONCLUSIONS: Mechanisms involved in the generation of a seizure that precedes a PET scan with fludeoxyglucose F 18 seem to influence the "interictal" hypometabolic pattern. Therefore, caution should be used when interpreting scans that are preceded by a nonhabitual seizure.

THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Basal ganglia involvement in temporal lobe epilepsy: A functional and morphologic study
Bouilleret et al.
Neurology 2008;70:177-184.
ABSTRACT | FULL TEXT  

Prognosis of children with partial epilepsy: MRI and serial 18FDG-PET
Gaillard et al.
Neurology 2007;68:655-659.
ABSTRACT | FULL TEXT  

Longitudinal Changes in Cortical Glucose Hypometabolism in Children With Intractable Epilepsy
Benedek et al.
J Child Neurol 2006;21:26-31.
ABSTRACT  

Dystonic posturing in seizures of mesial temporal origin: Electroclinical and metabolic patterns
Rusu et al.
Neurology 2005;65:1612-1619.
ABSTRACT | FULL TEXT  

Postoperative alteration of cerebral glucose metabolism in mesial temporal lobe epilepsy
Joo et al.
Brain 2005;128:1802-1810.
ABSTRACT | FULL TEXT  

Involvement of the Basal Ganglia in Refractory Epilepsy: An 18F-Fluoro-L-DOPA PET Study Using 2 Methods of Analysis
Bouilleret et al.
JNM 2005;46:540-547.
ABSTRACT | FULL TEXT  

Temporal lobe epilepsy with hippocampal sclerosis: predictors for long-term surgical outcome
Janszky et al.
Brain 2005;128:395-404.
ABSTRACT | FULL TEXT  

Medial temporal lobe epilepsy: gender differences
Janszky et al.
J. Neurol. Neurosurg. Psychiatry 2004;75:773-775.
ABSTRACT | FULL TEXT  

Limbic reductions of 5-HT1A receptor binding in human temporal lobe epilepsy
Savic et al.
Neurology 2004;62:1343-1351.
ABSTRACT | FULL TEXT  

Metabolic changes and electro-clinical patterns in mesio-temporal lobe epilepsy: a correlative study
Chassoux et al.
Brain 2004;127:164-174.
ABSTRACT | FULL TEXT  

Epileptic activity influences the speech organization in medial temporal lobe epilepsy
Janszky et al.
Brain 2003;126:2043-2051.
ABSTRACT | FULL TEXT  

Significance of interictal bilateral temporal hypometabolism in temporal lobe epilepsy
Koutroumanidis et al.
Neurology 2000;54:1811-1821.
ABSTRACT | FULL TEXT  

Interictal 18FDG PET Findings in Temporal Lobe Epilepsy With Deja vu
Adachi et al.
J. Neuropsychiatry Clin. Neurosi. 1999;11:380-386.
ABSTRACT | FULL TEXT  

Long term effects of refractory temporal lobe epilepsy on cognitive abilities: a cross sectional study
Jokeit and Ebner
J. Neurol. Neurosurg. Psychiatry 1999;67:44-50.
ABSTRACT | FULL TEXT  

Sex differences in patients with mesial temporal lobe epilepsy
Savic and Engel
J. Neurol. Neurosurg. Psychiatry 1998;65:910-912.
ABSTRACT | FULL TEXT  

Interictal regional slow activity in temporal lobe epilepsy correlates with lateral temporal hypometabolism as imaged with 18FDG PET: neurophysiological and metabolic implications
Koutroumanidis et al.
J. Neurol. Neurosurg. Psychiatry 1998;65:170-176.
ABSTRACT | FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1997 American Medical Association. All Rights Reserved.