Positron emission tomography imaging of tau pathology in progressive supranuclear palsy

被引:42
作者
Coakeley, Sarah [1 ,2 ]
Cho, Sang Soo [1 ,2 ]
Koshimori, Yuko [1 ,2 ]
Rusjan, Pablo [1 ]
Harris, Madeleine [1 ]
Ghadery, Christine [1 ,2 ]
Kim, Jinhee [1 ,2 ]
Lang, Anthony E. [3 ,4 ]
Wilson, Alan [1 ]
Houle, Sylvain [1 ]
Strafella, Antonio P. [1 ,2 ,3 ,4 ]
机构
[1] Univ Toronto, Campbell Family Mental Hlth Res Inst, Res Imaging Ctr, Ctr Addict & Mental Hlth, Toronto, ON, Canada
[2] Univ Toronto, Div Brain Imaging & Behav Syst Neurosci, Krembil Res Inst, UHN, Toronto, ON, Canada
[3] Univ Toronto, Morton & Gloria Shulman Movement Disorder Unit, Toronto Western Hosp, Neurol Div,Dept Med,UHN, Toronto, ON, Canada
[4] Univ Toronto, EJ Safra Program Parkinson Dis, Toronto Western Hosp, Neurol Div,Dept Med,UHN, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
Brain imaging; movement disorder; neuropathology; Parkinson's disease; positron emission tomography; ALZHEIMERS-DISEASE; RATING-SCALE; PET; PARKINSONISM; TAUOPATHIES; DIAGNOSIS; FEATURES; TRACER;
D O I
10.1177/0271678X16683695
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Progressive supranuclear palsy is a rare form of atypical Parkinsonism that differs neuropathologically from other parkinsonian disorders. While many parkinsonian disorders such as Parkinson's disease, Lewy body dementia, and multiple system atrophy are classified as synucleinopathies, progressive supranuclear palsy is coined a tauopathy due to the aggregation of pathological tau in the brain. [F-18] AV-1451 (also known as [F-18]-T807) is a positron emission tomography radiotracer that binds to paired helical filaments of tau in Alzheimer's disease. We investigated whether [F-18] AV-1451 could be used as biomarker for the diagnosis and disease progression monitoring in progressive supranuclear palsy. Six progressive supranuclear palsy, six Parkinson's disease, and 10 age-matched healthy controls were recruited. An anatomical MRI and a 90-min PET scan, using [F-18] AV-1451, were acquired from all participants. The standardized uptake value ratio from 60 to 90 min post-injection was calculated in each region of interest, using the cerebellar cortex as a reference region. No significant differences in standardized uptake value ratios were detected in our progressive supranuclear palsy group compared to the two control groups. [F-18] AV-1451 may bind selectivity to the paired helical filaments in Alzheimer's disease, which differ from the straight conformation of tau filaments in progressive supranuclear palsy.
引用
收藏
页码:3150 / 3160
页数:11
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