Quantification of [11C]choline uptake
using PET
[Methyl-11C]Choline
([11C]choline) is a marker for cellular
proliferation,
because choline is a precursor for the biosynthesis of phospholipids
which are the essential components of all cell membranes (Krohn, 2001).
Blood
Parent tracer represents 62% ± 19% of the
total radioactivity
in arterial plasma at 5 min after injection and 27% ± 12% at
15
min; the major metabolite in plasma is [11C]betaine
(Roivainen et al., 2000).
Tumors
Usefulness of
[11C]choline in the tumor diagnosis has been
demonstrated (Hara 2002), and quantification by using Gjedde-Patlak
plot (MTGA for irreversibly binding tracers), and SUV in
clinical setting has been validated (Utriainen et al., 2003; Sutinen et
al., 2004). However, cell proliferation may not explain the uptake
of [11C]choline in certain cancers
(Breeuwsma et al., 2005).
Rheumatoid arthritis
[
11C]Choline has been shown to accumulate in
clinically active synovitis, and the uptake (measured as
SUV and
net influx rate,
Ki)
correlated with the volume of synovium (Roivainen et al., 2003).
Initial uptake of [
11C]choline is very fast, and
the concentration of C-11 label reaches a plateau 10 min after
bolus injection (Roivainen et al., 2003; Roivainen &
Yli-Kerttula, 2006), suggesting irreversible kinetics during the PET
study length.
Gjedde-Patlak
plot (MTGA for irreversibly binding tracers) was linear
(Roivainen et al., 2003), confirming the irreversible uptake.
Furthermore, Gjedde-Patlak plot intercept with y axis was close to zero
(Roivainen et al., 2003), suggesting that calculation of Gjedde-Patlak
(requiring dynamic PET scanning) plot could quantitatively be replaced
by
FUR,
which only requires one late PET scan and enables whole-body imaging.
References:
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