For effective drug therapy of Parkinson's syndrome (PS), it is necessa
ry to distinguish between idiopathic and secondary genesis and PS in n
euronal systemic degeneration. [I-123]Iodobenzamide ([I-123] IBZM) is
a radiolabelled benzamide and binds specifically to the cerebral dopam
ine receptor (D-2) in the basal ganglia. The purpose of this study was
to determine the value of the [I-123]IBZM D-2-receptor SPECT in the d
ifferential diagnosis of PS. A total of 38 patients (20 females, 18 ma
les; age 61 +/- 13.3 years), with typical extrapyramidal symptoms were
investigated. Twenty suffered from idiopathic and 11 from secondary P
S. Seven patients in whom a neurological disease could be excluded, se
rved as controls. SPECT data were acquired 90 min after i.v. injection
of 185-200 MBq [I-123]IBZM. After reconstruction with a Butterworth f
ilter (cutoff frequency 0.5) and attenuation correction (coefficient 0
.12 cm(-1)) we quantify the IBZM basal ganglia uptake as ratio to the
frontal D-2-receptor-free cortex (BG/FC). The patients with idiopathic
PS (IPS) and the controls revealed high and specific IBZM uptake in t
he basal ganglia compared to the adjacent frontal brain tissue (IFS: B
G/ FC = 1.44 +/- 0.10; controls: BG/ FC = 1.48 +/- 0.10). A significan
t decreased striatal IBZM uptake is found in cases with secondary PS (
BG/FC = 1.25 +/- 0.10; p < 0.0001, t-test compared to controls and IFS
). The patient group with IFS can be subdivided into patients without
L-dopatherapy (BG/ FC = 1.49 +/- 0.07), patients with longstanding L-d
opa-therapy demonstrating significantly decreased striatal IBZM uptake
(BG/ FC = 1.31 +/- 0.04; p < 0.0001, t-test compared to controls and
other IFS), which correlates pathophysiological with a reduction of fr
ee D-2 receptors, and patients with de novo PS showing a slight increa
sed striatal IBZM uptake (BG/ FC = 1.56 +/- 0.05), which represents D-
2-receptor stimulation. [I-123] IBZM-SPECT is a sensitive and non-inva
sive test for striatal D-2-receptor density and activity which permits
relatively clear discrimination between idiopathic and secondary PS a
nd yields important information for differential therapy.