The 18F-fluorodeoxyglucose Lumped Constant Determined in Human Brain from Extraction Fractions of 18F-fluorodeoxyglucose and Glucose
Autor: | Gitte M. Knudsen, Peter Lund Madsen, Claus Svarer, Hanne Smith Pedersen, Olaf B. Paulson, Steen G. Hasselbalch, Søren Holm |
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Rok vydání: | 2001 |
Předmět: |
Cerebral glucose metabolism
030218 nuclear medicine & medical imaging 03 medical and health sciences 0302 clinical medicine Bolus (medicine) Positron Fluorodeoxyglucose F18 medicine Humans Bolus injection Fluorodeoxyglucose medicine.diagnostic_test Chemistry business.industry Brain Mean age Human brain carbohydrates (lipids) Glucose medicine.anatomical_structure Neurology Positron emission tomography Neurology (clinical) Cardiology and Cardiovascular Medicine Nuclear medicine business 030217 neurology & neurosurgery Tomography Emission-Computed medicine.drug |
Zdroj: | Journal of Cerebral Blood Flow & Metabolism. 21:995-1002 |
ISSN: | 1559-7016 0271-678X |
DOI: | 10.1097/00004647-200108000-00012 |
Popis: | Quantification of regional cerebral glucose metabolism (CMRglc) using positron emission tomography and 18F-fluorodeoxyglucose (PET-FDG) requires knowledge of the correction factor between FDG and glucose net clearance, the FDG lumped constant (LC). Because diverging values for LC have been obtained, the authors reevaluated LC by measuring the ratio of the cerebral net extraction fractions of FDG (E*) and glucose (E) from arteriovenous cerebral measurements. Thirty subjects were studied (mean age = 25 ± 4 years): 12 during a programed infusion of FDG and 18 after a bolus injection of FDG. In the infusion study, LC was calculated as the ratio E*/E. In the bolus study, E* was calculated from the slope of a Patlak–Gjedde plot. Lumped constant was significantly smaller in the infusion study as compared with the bolus study (0.48 ± 0.16 vs. 0.81 ± 0.27, P < 0.001). In 4 subjects studied during continuous FDG infusion for 2.5 hours, LC decreased to 0.36 ± 0.11. These results suggest that the “steady-state” method underestimates LC because E* continues to decline because of significant labeled product. Further, the authors provide evidence for resetting of LC toward a greater value. The subsequent resetting of CMRglc provides a physiologically more meaningful estimate and allows for comparison of CMRglc values between different methodologies. |
Databáze: | OpenAIRE |
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