We used qualitative visual assessment and semiquantitative measures of striatal DAT binding using [123I]FP-CIT-SPET in 85 patients with Parkinson's disease (PD). We compared these two assessments and their correlation with PD clinical progression. SPET imaging was visually classified by a nuclear medicine physician as normal or abnormal pattern grade I, II and III, in relation to a different degree of radioligand reduction uptake. Nineteen patients presented abnormal grade I (group 1), 53 grade II (group 2) and 13 grade III (group 3). The UPDRS III motor score, the H-Y score, the rigidity and bradykinesia subscores were significantly different among the three groups. Post hoc analysis showed that all values of these clinical parameters were higher in group 3 than in 2 and 1. All clinical indices were also significantly higher in group 2 than in group 1. This means that groups 3 and 2 were clinically more severely affected. No significant differences among the 3 groups were observed for age or duration of disease. Values of the mean striatum uptake were also significantly different among the three groups. Post hoc analysis revealed significantly lower values of the mean striatum uptake in group 3 with respect to groups 2 and 1; values were also significantly lower in group 2 than in group 1. We conclude that our findings of good consistency between visual and semi-quantitative assessment may help simplify the evaluation of striatal DAT binding in PD in a clinical routine setting.
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Univ Turku, Clin Neurosci, FI-20014 Turku, Finland
Turku Univ Hosp, Neuroctr, POB 52, FI-20521 Turku, Finland
Turku Univ Hosp, Turku PET Ctr, POB 52, FI-20521 Turku, FinlandUniv Turku, Clin Neurosci, FI-20014 Turku, Finland
Eklund, Mikael
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Nuuttila, Simo
Joutsa, Juho
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Univ Turku, Clin Neurosci, FI-20014 Turku, Finland
Turku Univ Hosp, Neuroctr, POB 52, FI-20521 Turku, Finland
Turku Univ Hosp, Turku PET Ctr, POB 52, FI-20521 Turku, Finland
Univ Turku, Turku Brain & Mind Ctr, FI-20014 Turku, FinlandUniv Turku, Clin Neurosci, FI-20014 Turku, Finland
Joutsa, Juho
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Jaakkola, Elina
Makinen, Elina
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Univ Turku, Clin Neurosci, FI-20014 Turku, Finland
Helsinki Univ Hosp HUS, Dept Neurol, Helsinki, Finland
Univ Helsinki HUS, Dept Clin Neurosci, POB 800, FI-00029 Helsinki, FinlandUniv Turku, Clin Neurosci, FI-20014 Turku, Finland
Makinen, Elina
Honkanen, Emma A.
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Univ Turku, Clin Neurosci, FI-20014 Turku, Finland
Turku Univ Hosp, Neuroctr, POB 52, FI-20521 Turku, Finland
Turku Univ Hosp, Turku PET Ctr, POB 52, FI-20521 Turku, FinlandUniv Turku, Clin Neurosci, FI-20014 Turku, Finland
Honkanen, Emma A.
Lindholm, Kari
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Univ Turku, Clin Neurosci, FI-20014 Turku, Finland
Turku Univ Hosp, Neuroctr, POB 52, FI-20521 Turku, FinlandUniv Turku, Clin Neurosci, FI-20014 Turku, Finland
Lindholm, Kari
Vahlberg, Tero
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Univ Turku, Biostat, Clin Med, POB 52, FI-20521 Turku, Finland
Turku Univ Hosp, POB 52, FI-20521 Turku, FinlandUniv Turku, Clin Neurosci, FI-20014 Turku, Finland
Vahlberg, Tero
Noponen, Tommi
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Turku Univ Hosp, Dept Clin Physiol & Nucl Med, POB 52, FI-20521 Turku, Finland
Turku Univ Hosp, Dept Med Phys, POB 52, FI-20521 Turku, FinlandUniv Turku, Clin Neurosci, FI-20014 Turku, Finland
Noponen, Tommi
Ihalainen, Toni
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Univ Helsinki, HUS Med Imaging Ctr, Clin Physiol & Nucl Med, POB 800, FI-00029 Helsinki, Finland
Helsinki Univ Hosp HUS, POB 800, FI-00029 Helsinki, FinlandUniv Turku, Clin Neurosci, FI-20014 Turku, Finland
Ihalainen, Toni
Murtomaki, Kirsi
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Helsinki Univ Hosp HUS, Dept Neurol, Helsinki, Finland
Univ Helsinki HUS, Dept Clin Neurosci, POB 800, FI-00029 Helsinki, FinlandUniv Turku, Clin Neurosci, FI-20014 Turku, Finland
Murtomaki, Kirsi
Nojonen, Tanja
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Helsinki Univ Hosp HUS, Dept Neurol, Helsinki, Finland
Univ Helsinki HUS, Dept Clin Neurosci, POB 800, FI-00029 Helsinki, FinlandUniv Turku, Clin Neurosci, FI-20014 Turku, Finland
Nojonen, Tanja
Levo, Reeta
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Helsinki Univ Hosp HUS, Dept Neurol, Helsinki, Finland
Univ Helsinki HUS, Dept Clin Neurosci, POB 800, FI-00029 Helsinki, FinlandUniv Turku, Clin Neurosci, FI-20014 Turku, Finland