Journal
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
Volume 74, Issue 3, Pages 294-298Publisher
BRITISH MED JOURNAL PUBL GROUP
DOI: 10.1136/jnnp.74.3.294
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Objectives: To examine the validity of [I-123]beta-CIT SPECT for monitoring the progression of dopaminergic degeneration in Parkinson's disease; to investigate the influence of short term treatment with D-2 receptor agonists on striatal [I-123]beta-CIT binding; and to determine the sample size and frequency of SPECT imaging required to demonstrate a significant effect of a putative neuroprotective agent. Methods: A group of 50 early stage Parkinson's disease patients was examined. Two SPECT imaging series were obtained, 12 months apart. The mean annual change in the ratio of specific to non-specific [I-123]beta-CIT binding to the striaturn, putamen, and caudate nucleus was used as the outcome measure. Results: A decrease in [I-123]beta-CIT binding ratios between the two images was found in all regions of interest. The average decrease in [I-123]beta-CIT binding ratios was about 8% in the whole striaturn, 8% in the putaminal region, and 4% in the caudate region. Comparison of scans done in nine patients under two different conditions-in the off state and while on drug treatment-showed no significant alterations in the expression of striatal dopamine transporters as measured using [I-123]beta-CIT SPECT. Power analysis indicated that to detect a significant (p < 0.05) effect of a neuroprotective agent with 0.80 power and 30% of predicted protection within two years, 216 patients are required in each group when the effects are measured in the whole putamen. Conclusions: [I-123]beta-CIT SPECT seems to be a useful tool to investigate the progression of dopaminergic degeneration in Parkinson's disease and may provide an objective method of measuring the effectiveness of neuroprotective treatments. Short term treatment with a D-2 agonist does not have a significant influence on [I-123]beta-CIT binding to dopamine transporters. If the latter finding is replicated in larger groups of patients, it supports the suitability of [I-123]beta-CIT SPECT for examining the progression of neurodegeneration in patients being treated with D-2 receptor agonists.
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