Upregulation of dopamine D2 receptors in dopaminergic drug-naive patients with parkin gene mutations

✍ Scribed by Christoph Scherfler; Naheed L. Khan; Nicola Pavese; Andrew J. Lees; Niall P. Quinn; David J. Brooks; Paola P. Piccini

• Publisher: John Wiley and Sons
• Year: 2006
• Tongue: English
• Weight: 96 KB
• Volume: 21
• Category: Article
• ISSN: 0885-3185
• DOI: 10.1002/mds.20811

✦ Synopsis

Abstract

Medicated patients with Parkinsonism and parkin gene mutations have been reported to show a significant decrease in striatal dopamine D~2~ receptors (D~2~R) in comparison to medicated idiopathic Parkinson's disease (IPD) patients with similar age and disease severity. The aim of this study was to verify whether the genetic defect per se is responsible for this decrease. We have studied with [^11^C]raclopride (RAC) positron emission tomography (PET) in a group of 14 sporadic patients with parkin‐linked Parkinsonism, 6 of whom had never received levodopa or dopamine agonists. The remaining 8 patients had been treated with levodopa for at least 5 years. Presynaptic striatal [^18^F]dopa storage was not significantly different between these two groups of patients. In untreated parkin‐positive patients, significant putaminal increases in RAC‐binding potential (BP) were found in comparison to an age‐matched healthy control group by using a classical region of interest approach and statistical parametric mapping. In contrast, levodopa‐treated parkin‐positive patients showed significant decreases in RAC‐BP in the caudate and putamen when compared to an age‐matched healthy control group. The RAC PET findings revealed that striatal D~2~R upregulation occurs in dopaminergic drug‐naive parkin‐positive patients, in a similar fashion to the upregulation reported in drug‐naive IPD. D~2~R downregulation observed in medicated parkin‐positive patients, therefore, is not caused primarily by the genetic defect itself. Parkin‐positive patients appear to have a greater susceptibility to the exposure to dopaminergic medication than IPD patients, which in turn might be an indirect effect of their genetic mutation. © 2006 Movement Disorder Society