Initial experience with [<sup>18</sup>F]DPA-714 TSPO-PET to image inflammation in primary angiitis of the central nervous system.
case_series · Level IV
Where this comes from
- Record sourced from PubMed, PMID 31960097.
- Also identified by DOI 10.1007/s00259-019-04662-4 and PMC identifier 7338821.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
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 [<sup>18</sup>F]DPA-714 to potentially assist differential diagnosis, therapy monitoring, and biopsy planning. In total, nine patients with ischemic stroke and diagnosed or suspected PACNS underwent [<sup>18</sup>F]DPA-714-PET-MRI. Dynamic PET scanning was performed for 60 min after injection of 233 ± 19 MBq [<sup>18</sup>F]DPA-714, and MRI was simultaneously acquired. In two PACNS patients, [<sup>18</sup>F]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 [<sup>18</sup>F]DPA-714-PET follow-up in a patient with PACNS showed reduced lesional [<sup>18</sup>F]DPA-714 uptake after anti-inflammatory treatment. Biopsy in the same patient pinpointed the source of tracer uptake to TSPO-expressing immune cells. [<sup>18</sup>F]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.
Medical subject headings
- Fluorine Radioisotopes
- Positron-Emission Tomography