As clinical PET becomes increasingly available, quantitative methods that a
re feasible in busy clinical settings are becoming necessary. We investigat
ed the use of intracranial blood pools as sources of an input function for
quantitative PET. Methods: We studied 25 patients after the intravenous inj
ection of [F-18]6-fluoro-L-m-tyrosine and compared sampled blood time-activ
ity curves with those obtained in small regions of interest (ROIs) defined
in the blood pools visible in the PET images. Because of the comparatively
large dimensions of the blood pool at the confluence of the superior sagitt
al, straight and transverse sinuses, a venous ROI input function was chosen
for further analysis, We applied simple corrections to the ROI-derived tim
e-activity curves, deriving expressions for partial volume, spillover and p
artition of tracer between plasma and red blood cells. The results of graph
ic and compartmental analysis using both sampled [C-s(t)] and ROI [C-r(t)]
venous input functions for each patient were compared. We also used an anal
ytic approach to examine possible differences between venous and arterial i
nput functions in the cerebral circulation. Results: C-r(t) peaked signific
antly earlier and higher than C-s(t) in this patient population, although t
he total integral under the curves did not differ significantly. We report
some apparent differences in the results of modeling using the two input fu
nctions; however, neither the graphically determined influx constant, K-i,
nor the model parameter that reflects presynaptic dopaminergic metabolism,
k(3), differed significantly between the two methods. The analytic results
suggest that the venous ROI input function may be closer to the arterial su
pply of radiotracer to the brain than arterialized venous blood, at least i
n some patient populations. Conclusion: We present a simple method of obtai
ning an input function for PET that is applicable to a wide range of tracer
s and quantitative methods and is feasible for diagnostic PET imaging.