DIFFERENTIAL DISTRIBUTION OF STRIATAL [(123)L]BETA-CIT IN PARKINSONS-DISEASE AND PROGRESSIVE SUPRANUCLEAR PALSY, EVALUATED WITH SINGLE-PHOTON EMISSION TOMOGRAPHY
C. Messa et al., DIFFERENTIAL DISTRIBUTION OF STRIATAL [(123)L]BETA-CIT IN PARKINSONS-DISEASE AND PROGRESSIVE SUPRANUCLEAR PALSY, EVALUATED WITH SINGLE-PHOTON EMISSION TOMOGRAPHY, European journal of nuclear medicine, 25(9), 1998, pp. 1270-1276
Functional imaging of the presynaptic dopaminergic activity using sing
le-photon emission tomography (SPET) and iodine-123 labelled 2-beta-ca
rboxymethoxy-3-beta-(4-iodophenyl)tropane ([I-123]beta-CIT) is importa
nt for the assessment of disease severity and progression in patients
with Parkinson's disease (PD). However, its capability to discriminate
between different extrapyramidal disorders has not yet been assessed.
The aim of this study was to evaluate the possibility of differentiat
ing patients with PD and with progressive supranuclear palsy (PSP) by
means of this method. The distribution of [I-123]beta-CIT in the basal
ganglia was assessed in six normal subjects, 13 petients with PD and
five patients with PSP in whom the disease was mild. SPET images were
obtained 24+/-2 h after i.v. injection of the tracer using a brain-ded
icated system (CERASPECT). MR and SPET images were co-registered in fo
ur normal subjects and used to define a standard set of 16 circular re
gions of interest (ROIs) on the slice showing the highest striatal act
ivity. The basal ganglia ROIs corresponded to (1) the head of caudate,
(2) a region of transition between the head of caudate and the anteri
or putamen, (3) the anterior putamen and (4) the posterior putamen. A
ratio of specific to non-displaceable striatal uptake was calculated n
ormalising the activity of the basal ganglia ROIs to that of the occip
ital cortex (V3 ''). ANOVA revealed a global reduction of V3 '' in all
ROIs of PD and PSP patients compared with normal controls (P<0.0001).
A Mann-Whitney U test showed that the difference between PD and PSP p
atients was statistically significant for the caudate region only (Z v
alue: 2.6; P<0.01). By subtracting V3 '' caudate values from those of
the putamen, differentiation from PSP was possible in 10/13 PD patient
s. In conclusion, analysis of [I-123]beta-CIT distribution in discrete
striatal areas provides information on the relative caudate-putamen d
amage, with different values being obtained in patients clinically dia
gnosed as having either PD or PSP.