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The pattern of FP-CIT PET in pure white matter hyperintensities–related vascular parkinsonism
Institution:1. Institute of Neuroscience, Newcastle University, Biomedical Research Building, Campus for Ageing and Vitality, Newcastle University, Newcastle upon Tyne, NE4 5PL, United Kingdom;2. Nuclear Medicine Department, Royal Victoria Infirmary, Newcastle upon Tyne NHS Foundation Hospitals Trust, Queen Victoria Road, Newcastle upon Tyne, NE1 4LP, United Kingdom;3. Department of Psychiatry, University of Cambridge, Box 189, Level E4 Cambridge Biomedical Campus, Cambridge, CB2 0SP, United Kingdom;1. Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea;2. Department of Biomedical Engineering, Hanyang University, Seoul, South Korea;3. Department of Neurology, Bundang Jesaeng General Hospital, Seongnam, South Korea;4. Department of Neurology, Yonsei University Wonju College of Medicine, Wonju, South Korea;5. Severance Biomedical Science Institute, Seoul, South Korea
Abstract:ObjectivesTo determine whether vascular parkinsonism (VaP) patients with visually normal dopamine transporter (DAT) scans have presynaptic dopaminergic depletion.MethodsWe enrolled 23 VaP patients who had parkinsonism, relevant diffuse subcortical white matter hyperintensities (WMH), and visually normal DAT scans, 23 Parkinson's disease (PD) patients, and 31 control subjects. By quantitatively analyzing 18F–N-(3-fluoropropyl)-2β-carbon ethoxy-3β-(4-iodophenyl) nortropane (18F-FP-CIT) positron emission tomography, we compared the pattern of striatal DAT availability among groups. The discriminatory power of striatal DAT availability to differentiate VaP patients from control subjects or PD patients was assessed using receiver operating characteristics (ROC) analyses. Additionally, correlation analysis was performed to determine whether WMH severity or Unified Parkinson Disease Rating Scale Part III (UPDRS-III) score is related to presynaptic dopaminergic depletion in VaP.ResultsVaP patients exhibited decreased DAT availability in all striatal subregions, including posterior putamen, compared to control subjects. VaP patients and control subjects had similar patterns of anteroposterior and ventrodorsal DAT gradients in caudate and putamen level, but VaP patients exhibited significantly different patterns at putamen level, relative to PD patients. The severity of periventricular WMH was significantly correlated with all substriatal DAT availability in VaP, but not with UPDRS-III scores. The ROC analysis showed that DAT availability in caudate and posterior putamen had a fair discriminatory power when differentiating VaP patients from control subjects.ConclusionsThis study demonstrates that VaP patients with WMH exhibited diffusely decreased DAT availability without any specific regional gradients of DAT patterns distinct from either control subjects or PD patients.
Keywords:Vascular parkinsonism  Dopamine transporter  White matter hyperintensity  Parkinson's disease
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