RT Journal Article
SR Electronic
T1 Hepatic Galactose Metabolism Quantified in Humans Using 2-18F-Fluoro-2-Deoxy-d-Galactose PET/CT
JF Journal of Nuclear Medicine
JO J Nucl Med
FD Society of Nuclear Medicine
SP 1566
OP 1572
DO 10.2967/jnumed.111.092924
VO 52
IS 10
A1 Michael Sørensen
A1 Kasper Sandager Mikkelsen
A1 Kim Frisch
A1 Ludvik Bass
A1 Bo Martin Bibby
A1 Susanne Keiding
YR 2011
UL http://jnm.snmjournals.org/content/52/10/1566.abstract
AB Accurate quantification of regional liver function is needed, and PET of specific hepatic metabolic pathways offers a unique method for this purpose. Here, we quantify hepatic galactose elimination in humans using PET and the galactose analog 2-18F-fluoro-2-deoxy-d-galactose (18F-FDGal) as the PET tracer. Methods: Eight healthy human subjects underwent 18F-FDGal PET/CT of the liver with and without a simultaneous infusion of galactose. Hepatic systemic clearance of 18F-FDGal was determined from linear representation of the PET data. Hepatic galactose removal kinetics were determined using measurements of hepatic blood flow and arterial and liver vein galactose concentrations at increasing galactose infusions. The hepatic removal kinetics of 18F-FDGal and galactose and the lumped constant (LC) were determined. Results: The mean hepatic systemic clearance of 18F-FDGal was significantly higher in the absence than in the presence of galactose (0.274 ± 0.001 vs. 0.019 ± 0.001 L blood/min/L liver tissue; P < 0.01), showing competitive substrate inhibition of galactokinase. The LC was 0.13 ± 0.01, and the 18F-FDGal PET with galactose infusion provided an accurate measure of the local maximum removal rate of galactose (Vmax) in liver tissue compared with the Vmax estimated from arterio-liver venous (A-V) differences (1.41 ± 0.24 vs. 1.76 ± 0.08 mmol/min/L liver tissue; P = 0.60). The first-order hepatic systemic clearance of 18F-FDGal was enzyme-determined and can thus be used as an indirect estimate of galactokinase capacity without the need for galactose infusion or knowledge of the LC. Conclusion: 18F-FDGal PET/CT provides an accurate in vivo measurement of human galactose metabolism, which enables the quantification of regional hepatic metabolic function.