Initial experience with [18F]DPA-714 TSPO-PET to image inflammation in primary angiitis of the central nervous system

被引:15
作者
Backhaus, Philipp [1 ,2 ]
Roll, Wolfgang [1 ]
Beuker, Carolin [3 ]
Zinnhardt, Bastian [1 ,2 ]
Seifert, Robert [1 ,2 ]
Wenning, Christian [1 ]
Eisenblaetter, Michel [4 ]
Thomas, Christian [5 ]
Schmidt-Pogoda, Antje [3 ]
Strunk, Daniel [3 ]
Wagner, Stefan [1 ]
Faust, Andreas [2 ]
Tuettelmann, Frank [6 ]
Roepke, Albrecht [6 ]
Jacobs, Andreas H. [2 ,7 ]
Stummer, Walter [8 ]
Wiendl, Heinz [3 ]
Meuth, Sven G. [3 ]
Schaefers, Michael [1 ,2 ]
Grauer, Oliver [3 ]
Minnerup, Jens [3 ]
机构
[1] Univ Hosp Munster, Dept Nucl Med, Munster, Germany
[2] Univ Munster, European Inst Mol Imaging, Munster, Germany
[3] Univ Hosp Munster, Dept Neurol, Inst Translat Neurol, Munster, Germany
[4] Univ Hosp Munster, Inst Clin Radiol, Munster, Germany
[5] Univ Hosp Munster, Inst Neuropathol, Munster, Germany
[6] Univ Hosp Munster, Inst Human Genet, Munster, Germany
[7] Johanniter Hosp, Dept Geriatr, Evangel Kliniken, Bonn, Germany
[8] Univ Hosp Munster, Dept Neurosurg, Munster, Germany
关键词
Search items; DPA-714; TSPO; Vasculitis; PET-MRI; Microglia; IN-VIVO; 18; KDA; MICROGLIAL ACTIVATION; TRANSLOCATOR PROTEIN; CEREBRAL VASCULITIS; ISCHEMIC-STROKE; NEUROINFLAMMATION; TOMOGRAPHY;
D O I
10.1007/s00259-019-04662-4
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose Primary angiitis of the central nervous system (PACNS) is a heterogeneous, rare, and poorly understood inflammatory disease. We aimed at non-invasive imaging of activated microglia/macrophages in patients with PACNS by PET-MRI targeting the translocator protein (TSPO) with [F-18]DPA-714 to potentially assist differential diagnosis, therapy monitoring, and biopsy planning. Methods In total, nine patients with ischemic stroke and diagnosed or suspected PACNS underwent [F-18]DPA-714-PET-MRI. Dynamic PET scanning was performed for 60 min after injection of 233 +/- 19 MBq [F-18]DPA-714, and MRI was simultaneously acquired. Results In two PACNS patients, [F-18]DPA-714 uptake patterns exceeded MRI correlates of infarction, whereas uptake was confined to the infarct in four patients where initial suspicion of PACNS could not be confirmed. About three patients with PACNS or cerebral predominant lymphocytic vasculitis showed no or only faintly increased uptake. Short-term [F-18]DPA-714-PET follow-up in a patient with PACNS showed reduced lesional [F-18]DPA-714 uptake after anti-inflammatory treatment. Biopsy in the same patient pinpointed the source of tracer uptake to TSPO-expressing immune cells. Conclusions [F-18]DPA-714-PET imaging may facilitate the diagnosis and treatment monitoring of PACNS. Further studies are needed to fully understand the potential of TSPO-PET in deciphering the heterogeneity of the disease.
引用
收藏
页码:2131 / 2141
页数:11
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