BackgroundA kinetic model analysis was recently proposed to estimate the
18F-fluorodeoxyglucose (18F-FDG) integrated activity in an
arbitrary tissue that uses tracer uptake and release rate constants. The aim
of the current theoretical paper was to estimate 18F-FDG
integrated activity using one standardized uptake value (SUV).MethodsA further kinetic model analysis allowed us to derive an analytical solution
for integrated activity determination, involving both irreversible and
reversible trapping. It only uses SUV, which is uncorrected for
18F physical decay (SUVuncorr, in
g.mL−1) and is assessed about its peak value.
Measurement uncertainty of the estimate was also assessed.ResultsIn a tissue (volume V, in mL) that irreversibly traps
18F-FDG, the total number of disintegrations can be estimated as:
ÃC = 162 * 105 *
SUVuncorr * V * ID / W
(ID, injected dose, in MBq; W, patient’s weight,
in kg), where SUVuncorr is a mean over V and is assessed
between 55 and 110 min after tracer injection. The relative uncertainty
ranges between 18% and 30% (the higher the uptake, the lower the
uncertainty). Comparison with the previous Zanotti-Fregonara’s model
applied to foetus showed less than 16% difference. Furthermore, calculated
integrated activity estimates were found in good agreement with
Mejia’s results for healthy brain, lung and liver that show various
degrees of tracer trapping reversibility and various fractions of free
tracer in blood and interstitial volume.ConclusionEstimation of integrated activity in an arbitrary tissue using one SUV value
is possible, with measurement uncertainty related to required assumptions. A
formula allows quick estimation that does not underestimate integrated
activity so that it could be helpful in circumstances such as accidental
exposure, or for epidemiologic purposes such as in patients having undergone
several examinations.