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Departments of Neurology, Research, Medicine and Biostatistics, North Shore University Hospital/Cornell University Medical College, Manhasset, New York
Correspondence: For correspondence or reprints contact: Dr. David Eidelberg, Dept. of Neurology, North Shore University Hospital/Cornell University Medical College, 300 Community Dr., Manhasset, New York 11030.
ABSTRACT
PET has been used to quantify striatal 6-[18F]fluoro-L-dopa (FDOPA) uptake as a measure of presynaptic dopaminergic function. Striatal FDOPA uptake rate constants (K1) can be calculated using dynamic PET imaging with measurements of the plasma FDOPA input function determined either directly or by several estimation procedures. Methods: We assessed the comparative clinical utility of these methods by calculating the striato-occipital ratio (SOR) and striatal K1 values in 12 patients with mild to moderate PD and 12 age-matched normal volunteers. The plasma FDOPA time-activity curve (K1FD); the plasma 18F time-activity curve (K1P); the occipital time-activity curve (K1OCC); and a simplified population-derived FDOPA input function (K1EFD) were used to calculate striatal K1. Results: Mean values for all striatal K1 estimates and SOR were significantly lower in the PD group. Although all measured parameters discriminated PD patients from normals, K1FD and K1EFD provided the best between-group separation. K1FD, K1EFD and K1OCC measures correlated significantly with quantitative disease severity ratings, although K1FD predicted quantitative clinical disability most accurately. Conclusion: These results suggest that K1FD may be an optimal marker of the parkinsonian disease process. K1EFD may be a useful alternative to K1FD for most clinical research applications.
Key Words: PET 6-[18F]fluoro-L-dopa input function multiple time graphical approach Parkinson's disease discriminant analysis nigrostriatal dopaminergic function
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