Regional lumped constant differences and asymmetry in fluorine-18-FDG uptake in temporal lobe epilepsy

David C. Reutens, Albert H. Gjedde, Ernst Meyer

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

To date, there has been no satisfactory explanation for the observation that interictal uptake of the glucose analog [18F]fluorodeoxyglucose (FDG) is consistently reduced in the temporal lobe ipsilateral to the seizure focus in patients with temporal lobe epilepsy. We examined the hypothesis that regional differences in tracer uptake in temporal lobe epilepsy reflect regional differences in the lumped constant (Λ). Methods: In 9 control subjects and 10 patients with temporal lobe epilepsy, we obtained regional estimates of Λ by expressing Λ in terms of transfer coefficients for FDG and parameters which are likely to remain constant throughout both the brain and under different functional states. Results: In the patients, Λ was lower in the temporal lobe ipsilateral to the epileptic focus (0.53 ± 0.06; p < 0.005) than in the contralateral temporal lobe (0.56 ± 0.06). Interside differences in Λ were highly correlated with asymmetry in tracer uptake. Furthermore, the use of regional estimates of Λ reduced the asymmetry in estimated rCMR(glc) in patients with temporal lobe epilepsy but not in controls. Conclusion: In these patients, a change in tracer uptake may not indicate a change in glucose consumption of corresponding magnitude, raising the possibility that in at least some patients with temporal lobe epilepsy, the term hypometabolism does not accurately describe reductions in tracer uptake.

Original languageEnglish (US)
Pages (from-to)176-180
Number of pages5
JournalJournal of Nuclear Medicine
Volume39
Issue number1
StatePublished - Jan 1 1998

Keywords

  • Fluorine-18-fluorodeoxyglucose
  • PET
  • Temporal lobe epilepsy

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging

Fingerprint

Dive into the research topics of 'Regional lumped constant differences and asymmetry in fluorine-18-FDG uptake in temporal lobe epilepsy'. Together they form a unique fingerprint.

Cite this