E. Broussolle et al., The relation of putamen and caudate nucleus F-18-Dopa uptake to motor and cognitive performances in Parkinson's disease, J NEUR SCI, 166(2), 1999, pp. 141-151
The contribution of striatal (caudate nucleus-putamen) dopaminergic deficie
ncy to the severity of motor signs is well established in Parkinson's disea
se (PD), while its role in the occurrence of cognitive and mood changes rem
ains unresolved. We therefore measured in 27 non-demented PD patients and 1
0 age-matched controls striatal uptake of [F-18]-6-fluoro-L-Dopa (F-Dopa) w
ith PET, and mood (Beck depression), memory (Grober-Buschke), frontal execu
tive functions (verbal fluency and Wisconsin card sorting), and attentional
processing of sensory stimuli (N2-P3 auditory event-related potentials - E
RPs). Locomotor disability of patients was assessed by Hoehn and Yahr score
and Unified Parkinson's Disease Rating Scale (UPDRS), ANOVA showed that me
mory, but neither frontal lobe functions nor ERPs, was significantly altere
d in PD patients, whereas indices of depression were found only in advanced
PD. The F-Dopa rate constant K-i was significantly reduced in the striatum
, more in putamen than caudate nucleus, and inversely correlated with disea
se duration. A significant inverse correlation was found between both putam
en and caudate nucleus Ki and Hoehn and Yahr score, and between putamen - b
ut not caudate nucleus K-i - and UPDRS motor score, Principal components an
alysis (PCA) of PD patients K-i values and mood, cognitive and ERP paramete
rs gave a three-factor solution. Variables contributing to factor 1 were me
mory score and N2-P3 ERP latencies, those to factor 2 were striatal K-i val
ues, and those to factor 3 frontal executive performances. Depression did n
ot segregate with any variable. Our findings suggest that unlike locomotor
disability, cognitive abilities and mood state of non-demented PD patients
are for the most part unrelated to striatal dopaminergic depletion and may
result from dysfunction of extra-striatal dopaminergic or from non-dopamine
rgic systems. (C) 1999 Elsevier Science B.V. All rights reserved.