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EDITORIAL COMMENTARY |
| Parkinsons disease |
Auckland Hospital, New Zealand;
bsnow@adhb.govt.nz
Keywords: Parkinsons disease; SPECT; PET
| The first 150 words of the full text of this article appear below. |
A persisting frustration in the diagnosis, treatment, and research of Parkinsons disease is the lack of an objective measure of the nigrostriatal dopaminergic deficit. In particular, we need a tool to monitor the progress of the neuronal degeneration. This is very difficult to achieve clinically in Parkinsons disease because of the complex clinical presentation and the confounding effect of symptomatic therapy. Although PET, with markers of presynaptic dopaminergic function such as 6-fluorodopa, is an accepted measuring tool, PET is complex, expensive, cumbersome, and not widely available. The alternative is SPECT, and Winogrodzka et al on pp 2942981 of this issue provide evidence that SPECT does the job.
Winogrodzka et al took 50 patients with Parkinsons disease and performed SPECT scans 12 months apart. For their tracer, they chose [123I] ß-CIT, which binds to the presynaptic dopamine transporters. They showed an 8% decline in binding density. This matches
Related Article
J. Neurol. Neurosurg. Psychiatry 2003 74: 294-298.
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