The pattern of FP-CIT PET in pure white matter hyperintensities–related vascular parkinsonism
To determine whether vascular parkinsonism (VaP) patients with visually normal dopamine transporter (DAT) scans have presynaptic dopaminergic depletion. We enrolled 23 VaP patients who had parkinsonism, relevant diffuse subcortical white matter hyperintensities (WMH), and visually normal DAT scans,...
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Published in | Parkinsonism & related disorders Vol. 82; pp. 1 - 6 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Ltd
01.01.2021
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Subjects | |
Online Access | Get full text |
ISSN | 1353-8020 1873-5126 1873-5126 |
DOI | 10.1016/j.parkreldis.2020.11.002 |
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Abstract | To determine whether vascular parkinsonism (VaP) patients with visually normal dopamine transporter (DAT) scans have presynaptic dopaminergic depletion.
We 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.
VaP 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.
This 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.
•VaP with normal DAT scan exhibited decreased striatal SNBRs compared to controls.•Unlike PD, VaP had a more diffuse loss of DAT availability across whole striatum.•Severity of periventricular WMH was correlated with all substriatal SNBRs in VaP.•SNBRs of AC, PC, and PP had a fair accuracy when discriminating VaP from controls. |
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AbstractList | To determine whether vascular parkinsonism (VaP) patients with visually normal dopamine transporter (DAT) scans have presynaptic dopaminergic depletion.
We 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.
VaP 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.
This 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.
•VaP with normal DAT scan exhibited decreased striatal SNBRs compared to controls.•Unlike PD, VaP had a more diffuse loss of DAT availability across whole striatum.•Severity of periventricular WMH was correlated with all substriatal SNBRs in VaP.•SNBRs of AC, PC, and PP had a fair accuracy when discriminating VaP from controls. To determine whether vascular parkinsonism (VaP) patients with visually normal dopamine transporter (DAT) scans have presynaptic dopaminergic depletion. We 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 F-N-(3-fluoropropyl)-2β-carbon ethoxy-3β-(4-iodophenyl) nortropane ( F-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. VaP 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. This 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. To determine whether vascular parkinsonism (VaP) patients with visually normal dopamine transporter (DAT) scans have presynaptic dopaminergic depletion.OBJECTIVESTo determine whether vascular parkinsonism (VaP) patients with visually normal dopamine transporter (DAT) scans have presynaptic dopaminergic depletion.We 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.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.VaP 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.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.This 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.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. |
Author | Yun, Mijin Jung, Jin Ho Sohn, Young H. Chung, Seok Jong Lee, Yang Hyun Ye, Byoung Seok Lee, Phil Hyu Yoo, Han Soo Lee, Sangwon Baik, Kyoungwon |
Author_xml | – sequence: 1 givenname: Yang Hyun surname: Lee fullname: Lee, Yang Hyun email: lyhkjgo@gmail.com organization: Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea – sequence: 2 givenname: Sangwon surname: Lee fullname: Lee, Sangwon email: lsw0423@yuhs.ac organization: Department of Nuclear Medicine, Yonsei University College of Medicine, Seoul, South Korea – sequence: 3 givenname: Seok Jong surname: Chung fullname: Chung, Seok Jong email: pyh6001@hanmail.net organization: Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea – sequence: 4 givenname: Han Soo surname: Yoo fullname: Yoo, Han Soo email: omsavior7@gmail.com organization: Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea – sequence: 5 givenname: Jin Ho surname: Jung fullname: Jung, Jin Ho email: jhjung@yuhs.ac organization: Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea – sequence: 6 givenname: Kyoungwon surname: Baik fullname: Baik, Kyoungwon email: baikkw@yuhs.ac organization: Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea – sequence: 7 givenname: Byoung Seok surname: Ye fullname: Ye, Byoung Seok email: romel79@yuhs.ac organization: Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea – sequence: 8 givenname: Young H. surname: Sohn fullname: Sohn, Young H. email: yhsohn62@yuhs.ac organization: Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea – sequence: 9 givenname: Mijin surname: Yun fullname: Yun, Mijin email: yunmijin@yuhs.ac organization: Department of Nuclear Medicine, Yonsei University College of Medicine, Seoul, South Korea – sequence: 10 givenname: Phil Hyu surname: Lee fullname: Lee, Phil Hyu email: phlee@yuhs.ac organization: Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea |
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CitedBy_id | crossref_primary_10_1002_ird3_121 crossref_primary_10_1016_j_parkreldis_2021_11_033 crossref_primary_10_1136_bmjment_2024_301042 crossref_primary_10_4103_1673_5374_391180 crossref_primary_10_1007_s13139_024_00840_x crossref_primary_10_1016_j_ensci_2024_100528 |
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Keywords | White matter hyperintensity Dopamine transporter Parkinson's disease Vascular parkinsonism |
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Relat. Disord. doi: 10.1016/j.parkreldis.2017.12.030 |
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Snippet | To determine whether vascular parkinsonism (VaP) patients with visually normal dopamine transporter (DAT) scans have presynaptic dopaminergic depletion.
We... To determine whether vascular parkinsonism (VaP) patients with visually normal dopamine transporter (DAT) scans have presynaptic dopaminergic... |
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SubjectTerms | Dopamine transporter Parkinson's disease Vascular parkinsonism White matter hyperintensity |
Title | The pattern of FP-CIT PET in pure white matter hyperintensities–related vascular parkinsonism |
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