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The Discriminating Nature of Dopamine Transporter Image in Parkinsonism: The Competency of Dopaminergic Transporter Imaging in Differential Diagnosis of Parkinsonism: $^{123}I-FP-CIT$ SPECT Study  

Kim, Bom-Sahn (Departments of Nuclear Medicine, Seoul National University College of Medicine)
Jang, Sung-June (Departments of Nuclear Medicine, Seoul National University College of Medicine)
Eo, Jae-Seon (Departments of Nuclear Medicine, Seoul National University College of Medicine)
Park, Eun-Kyung (Departments of Nuclear Medicine, Seoul National University College of Medicine)
Kim, Yu-Kyeong (Departments of Nuclear Medicine, Seoul National University College of Medicine)
Kim, Jong-Min (Departments of Neurology, Seoul National University College of Medicine)
Lee, Won-Woo (Departments of Nuclear Medicine, Seoul National University College of Medicine)
Kim, Sang-Eun (Departments of Nuclear Medicine, Seoul National University College of Medicine)
Publication Information
Nuclear Medicine and Molecular Imaging / v.41, no.4, 2007 , pp. 272-279 More about this Journal
Abstract
Purpose: The aim of this study was to evaluate the discriminating nature of $^{123}I-FP-CIT$ SPECT in patients with parkinsonism. Methods: $^{123}I-FP-CIT$ SPECT images acquired from the 18 normal controls; NC ($60.4{\pm}10.0$ yr) and 237 patients with parkinsonism ($65.9{\pm}9.2$ yr) were analyzed. From spatialIy normalized images, regional counts of the caudate, putamen, and occipital lobe were obtained using region of interest method. Binding potential (BP) was calculated with the ratio of specific to nonspecific binding activity at equilibrium. Additionally, the BP ratio of putamen to caudate (PCR) and asymmetric Index (ASI) were measured. Results: BPs of NC $3.37{\pm}0.57,\; 3.10{\pm}0.41,\; 3.23{\pm}0.48$ for caudate, putamen, whole striatum, respectively) had no significant difference with those of essential tremor; ET ($3.31{\pm}0.64,\; 3.06{\pm}0.61,\; 3.14{\pm}0.63$) and Alzheimer's disease; AD (3.33 $\pm$0.60, 3.29$\pm$0.79, 3.31$\pm$0.70), but were higher than those of Parkinson's disease; PD (1.92$\pm$0.74, 1.39$\pm$0.68, 1.64$\pm$0.68), multiple system atrophy; MSA (2.36$\pm$1.07, 2.16$\pm$0.91, 2.26$\pm$0.96), and dementia with Lewy body; DLB (1.95$\pm$0.72, 1.64$\pm$0.65, 1.79$\pm$0.66)(p<0.005). PD had statisticalIy lower values of PER and higher values of ASI than those of NC (p<0.005). And PD had significantIy lower value of PCR, higher ASI and lower BP in the putamen and whole striatum than MSA (p<0.05). Conclusion: Dopamine transporter image of $^{123}I-FP-CIT$ SPECT was a good value in differential diagnosis of parkinsonism.
Keywords
dopamine transporter; parkinsonism; $^{123}I-FP-CIT$; Parkinson's disease; binding potential;
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1 Chui HC, Teng EL, Henderson VW, Moy AC. Clinical subtypes of dementia of the Alzheimer type. Neurology. 1985;35:1544-50   DOI
2 Kemppainen N, Ruottinen H, Ngren K, Rinne JO. PET shows that striatal dopamine D1 and D2 receptors are differentially affected in AD. Neurology. 2000;55:205-9   DOI   ScienceOn
3 Ceravolo R, Volterrani D, Gambaccini G, Bernardini S, Rossi C, Logi C, et al. Presynaptic nigro-striatal function in a group of Alzheimer's disease patients with parkinsonism: evidence from a dopamine transporter imaging study. J Neural Transm. 2004;111: 1065-73. Epub 2004 Jun 18
4 Walker Z, Costa DC, Walker RW, Lee L, Livingston G, Jaros E, et al. Striatal dopamine transporter in dementia with Lewy bodies and Parkinson disease: a comparison. Neurology. 2004;60:1568-72
5 McKeith IG. Spectrum of Parkinson's disease, Parkinson's dementia, and Lewy body dementia. Neurol Clin. 2000;18:865-902   DOI
6 Kosaka K, Iseki E.: Diffuse Lewy body disease within the spectrum of Lewy body disease. In: Perry R, McKeith I, Perry E (eds): Dementia with Lewy Bodies. New York, Cambridge University Press, 1996, pp 238-47
7 Lavalaye J, Booij J, Reneman L, Habraken JB, van Royen EA. Effect of age and gender on dopamine transporter imaging with [$^{123}I$]FP-CIT SPET in healthy volunteers. Eur J Nucl Med. 2000;27:867-9   DOI
8 Nurmi E, Ruottinen HM, Kaasinen V, Bergman J, Haaparanta M, Solin O, et al. Progression in Parkinson's disease: a positron emission tomography study with a dopamine transporter ligand [$^{18}F]CFT. Ann Neurol. 2000;47:804-8   DOI   ScienceOn
9 Morrish PK, Rakshi JS, Bailey DL, Sawle GV, Brooks DJ. Measuring the rate of progression and estimating the preclinical period of Parkinson's disease with [$^{18}F]dopa PET. J Neurol Neurosurg Psychiatry. 1998;64:314-9   DOI
10 Morrish PK, Sawle GV, Brooks DJ. An [$^{18}F]dopa-PET and clinical study of the rate of progression in Parkinson's disease. Brain. 1996;119:585-91   DOI   ScienceOn
11 Whone AL, Watts RL, Stoessl AJ, Davis M, Reske S, Nahmias C, et al. Slower progression of Parkinson's disease with ropinirole versus levodopa: The REAL-PET study. Ann Neurol. 2003;54: 93-101   DOI   ScienceOn
12 Nurmi E, Ruottinen HM, Bergman J, Haaparanta M, Solin O, Sonninen P, et al. Rate of progression in Parkinson's disease: a 6-[$^{18}F$]fluoro-L-dopa PET study. Mov Disord. 2001;16:608-15   DOI   ScienceOn
13 Niznik HB, Fogel EF, Fassos FF, Seeman P. The dopamine transporter is absent in parkinsonian putamen and reduced in caudate nucleus. J Neurochem. 1991;56:192-8   DOI
14 Donnemiller E, Heilmann J, Wenning GK, Berger W, Decristoforo C, Moncayo R, et al. Brain perfusion scintigraphy with $^{99m}Tc$-HMPAO or $^{99m}Tc$-ECD and 123I-beta-CIT single-photon emission tomography in dementia of the Alzheimer-type and diffuse Lewy body disease. Eur J Nucl Med. 1997;24:320-5   DOI
15 Mayeux R, Stern Y, Spanton S. Heterogeneity in dementia of the Alzheimer type: evidence of subgroups. Neurology. 1985;35:453-61   DOI
16 Perneczky R, Msch D, Neumann M, Kretzschmar H, Mller U, Busch R, et al. The Alzheimer Variant of Lewy Body Disease: A Pathologically Confirmed Case-Control Study. Dement Geriatr Cogn Disord. 2005;20:89-94   DOI   ScienceOn
17 Jeon B, Kim JM, Jeong JM, Kim KM, Chang YS, Lee DS, et al. Dopamine transporter imaging with [$^{123}I$]--CIT demonstrates presynaptic nigrostriatal dopaminergic damage in Wilson's disease. J Neurol Neurosurg Psychiatry. 1998;65:60-4   DOI
18 Niznik HB, Fogel EF, Fassos FF, Seeman P. The dopamine transporter is absent in parkinsonian putamen and reduced in the caudate nucleus. J Neurochem. 1991;56:192-8   DOI
19 O'Brien JT, Colloby S, Fenwick J, Williams ED, Firbank M, Burn D, et al. Dopamine transporter loss visualized with FP-CIT SPECT in the differential diagnosis of dementia with Lewy bodies. Arch Neurol. 2004;61:919-25   DOI   ScienceOn
20 Booij J, Tissingh G, Boer GJ, Speelman JD, Stoof JC, Janssen AG, et al. [$^{123}I$]FP-CIT SPECT shows a pronounced decline of striatal dopamine transporter labelling in early and advanced Parkinson's disease. J Neurol Neurosurg Psychiatry. 1997;62:133-40   DOI   ScienceOn
21 Neumeyer JL, Wang SY, Milius RA, Baldwin RM, Zea-Ponce Y, Hoffer PB, et al.[$^{123}I$]-2-$\beta$-Carbomethoxy-3-$\beta$-(4-iodo-phenyl)- tropane ($\beta$-CIT). High affinity SPECT radiotracer of monoamine reuptake sites in brain. J Med Chem. 1991;34:3144-6   DOI
22 Walker Z, Costa DC, Walker RW, Shaw K, Gacinovic S, Stevens T, et al. Differentiation of dementia with Lewy bodies from Alzheimer's disease using a dopaminergic presynaptic ligand. J Neurol Neurosurg Psychiatry. 2002;73:134-40   DOI
23 Kim SE, Choi JY, Choe YS, Choi Y, Lee WY. Serotonin transporters in the midbrain of Parkinson's disease patients: a study with $^{123}I$-beta-CIT SPECT. J Nucl Med. 2003;44:870-6
24 Kaufman MJ, Madras BK. Severe depletion of cocaine recognition sites associated with the dopamine transporter in Parkinson's disease striatum. Synapse. 1991;9:43-9   DOI   ScienceOn
25 Kaufman MJ, and Madras BK. Severe depletion of cocaine recognition sites associated with the dopamine transporter in Parkinson's diseased striatum, Synapse. 1991;9;43-9   DOI   ScienceOn
26 Wang J, Zuo CT, Jiang YP, Guan YH, Chen ZP, Xiang JD, et al. $^{18}F-FP-CIT PET imaging and SPM analysis of dopamine transporters in Parkinson's disease in various Hoehn & Yahr stages. J Neurol. 2007;254:185-90   DOI
27 Booij J, Andringa G, Rijks LJ, Vermeulen RJ, De Bruin K, Boer GJ, et al. [$^{123}I$]FP-CIT binds to the dopamine transporter as assessed by biodistribution studies in rats and SPECT studies in MPTPlesioned monkeys. Synapse. 1997;27:183-90   DOI   ScienceOn
28 Winogrodzka A, Bergmans P, Booij J, van Royen EA, Janssen AG, Wolters EC. [$^{123}I$]FP-CIT SPECT is a useful method to monitor the rate of dopaminergic degeneration in early-stage Parkinson's disease. J Neural Transm. 2001;108:1011-9   DOI
29 Benamer TS, Patterson J, Grosset DG, Booij J, de Bruin K, van Royen E, et al. Accurate differentiation of parkinsonism and essential tremor using visual assessment of [123I]-FP-CIT SPECT imaging: the [$^{123}I$]-FP-CIT study group. Mov Disord. 2000;15: 503-10   DOI   ScienceOn
30 Van Laere K, Casteels C, De Ceuninck L, Vanbilloen B, Maes A, Mortelmans L, et al. Dual-tracer dopamine transporter and perfusion SPECT in differential diagnosis of parkinsonism using template-based discriminant analysis. J Nucl Med. 2006;47:384-92
31 Booij J, Habraken JB, Bergmans P, Tissingh G, Winogrodzka A, Wolters EC, et al. Imaging of dopamine transporters with Iodine-123-FPCIT SPECT in healthy controls and patients with Parkinson's disease. J Nucl Med. 1998;39:1879-84
32 Tissingh G, Booij J, Bergmans P, Winogrodzka A, Janssen AG, van Royen EA, et al. Iodine-123-N-omega-fluoropropyl-2$\beta$-carbomethoxy- 3$\beta$-(4-iodophenyl)tropane SPECT in healthy controls and early-stage, drug-naive Parkinson's disease. J Nucl Med. 1998;39: 1143-8
33 Pizzolato G, Chierichetti F, Fabbri M, Cagnin A, Dam M, Ferlin G, et al. Reduced striatal dopamine receptors in Alzheimer's disease: single photon emission tomography study with the D2 tracer [$^{123}I$]-IBZM. Neurology. 1996;47:1065-8   DOI   ScienceOn
34 de Rijk MC, Tzourio C, Breteler MM, Dartigues JF, Amaducci L, Lopez-Pousa S, et al. Prevalence of parkinsonism and Parkinsons disease in Europe: the EUROPARKINSON collaborative study. European community concerted action on the epidemiology of Parkinsons disease. J Neurol Neurosurg Psychiatry. 1997;62:10-5   DOI
35 Parkinson Study Group. A multicenter assessment of dopamine transporter imaging with DOPASCAN/SPECT in parkinsonism. Neurology. 2000; 55:1540-7   DOI   ScienceOn
36 Hughes AJ, Daniel SE, Lees AJ. Improved accuracy of clinical diagnosis of Lewy body Parkinson's disease. Neurology. 2001;57: 1497-9   DOI   ScienceOn
37 Van Laere K, Casteels C, De Ceuninck L, Vanbilloen B, Maes A, Mortelmans L, et al. Dual-tracer dopamine transporter and perfusion SPECT in differential diagnosis of parkinsonism using templatebased discriminant analysis. J Nucl Med. 2006;47:384-92
38 Hughes AJ, Daniel SE, Kilford L, Lees AJ. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. J Neurol Neurosurg Psychiatry. 1992;55:181-4   DOI
39 Colloby S, O'Brien J. Functional imaging in Parkinson's disease and dementia with Lewy bodies. J Geriatr Psychiatry Neurol. 2004;17: 158-63   DOI