## Abstract Atypical parkinsonian syndromes (APS) such as multiple system atrophy, progressive supranuclear palsy, and corticobasal degeneration are characterized by poor response to antiparkinsonian medication and rapid clinical deterioration. We used SPECT and [^123^I]β‐CIT as a label of dopamine
Measuring the rate of progression of Parkinson's disease over a 5-year period with β-CIT SPECT
✍ Scribed by Walter Pirker; Iris Holler; Willibald Gerschlager; Susanne Asenbaum; Georg Zettinig; Thomas Brücke
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 81 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0885-3185
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✦ Synopsis
Abstract
Recent imaging studies suggest a rapid degeneration of the dopaminergic system in early Parkinson's disease (PD), followed by a slowing of the degenerative process in advanced disease. In the present study, a group of early‐stage PD patients underwent three sequential [^123^I]β‐CIT SPECT studies to assess the decline of striatal dopamine transporter binding over a 5‐year period. Twenty‐one of a cohort of 24 early PD patients who participated in an earlier longitudinal β‐CIT SPECT imaging study [Mov Disord 2002;17:45–53] were included. Scan intervals were 26 ± 11 months (scan 1–2) and 38 ± 15 months (scan 2–3), respectively. The relative annual rate of decline of striatal β‐CIT binding from age‐expected normal values at the time of Scan 1 was used as primary outcome variable. The relative annual decline of striatal binding from Scan 1 to Scan 2 (4.5 ± 4.6%) and from Scan 2 to Scan 3 (3.0 ± 3.0%) was not significantly different. The non‐significant difference in progression rate was due mainly to the rapid early decline of striatal binding in 1 patient who subsequently developed a severe dysexecutive dementia syndrome. These data are not suggestive of substantial change in the course of dopaminergic degeneration in PD within the first 5 to 7 years after symptom onset. © 2003 Movement Disorder Society
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