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From the Departments of Neurology (Drs. Kaasinen and Rinne), Psychiatry (Dr. Hietala), and Pharmacology (Dr. Vilkman), University of Turku, and the Turku PET Centre (Drs. Någren and Oikonen), Turku, Finland; and the Department of Clinical Neuroscience (Drs. Farde and Halldin), Karolinska Hospital, Stockholm, Sweden.
Address correspondence and reprint requests to Dr. Valtteri Kaasinen, Department of Neurology, University of Turku, Turku FIN-20520, Finland; e-mail: valtteri.kaasinen{at}pet.tyks.fi
OBJECTIVE: To investigate whether dopamine D2 and D3 receptor subtypes (D2/3Rs) outside the caudate-putamen are affected in PD.
BACKGROUND: Alterations in striatal D2-like dopamine receptors in PD have been extensively demonstrated using PET, but there are no studies focusing on extrastriatal D2/3Rs.
METHODS: Fourteen unmedicated patients with idiopathic early PD with predominantly left-sided symptoms, 14 levodopa-medicated patients with advanced PD, and 20 normal age-matched controls were examined using PET. PET scanning was performed with a novel high-affinity D2/3R radioligand ([11C]FLB 457) and a PET scanner in three-dimensional mode.
RESULTS: In advanced PD, the binding potential of [11C]FLB 457 in the dorsolateral prefrontal cortex was decreased by 40% (p < 0.01), in the anterior cingulate cortex by 20% (p < 0.01), and in the medial thalamus by 17% (p < 0.05) compared with healthy controls. In early PD, the extrastriatal [11C]FLB 457 binding potentials were not significantly different compared with the control group. However, the binding potential in the anterior cingulate cortex (29%; p < 0.05) was higher in early PD compared with advanced PD.
CONCLUSIONS: These results imply that the D2/3 receptor subtypes outside the striatum are affected in advanced PD but not in the early stages of the disease, and that this receptor decline is present in the anterior cingulate cortex, the dorsolateral prefrontal cortex, and the thalamus.
Key words: PDDopamine receptorsD2 subtypeD3 subtype
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