Journal Article DZNE-2026-00851

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Feasibility of short imaging protocols for [18F]fluordeprenyl-D2 PET in autoimmune encephalitis and multiple system atrophy.

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2026
Springer-Verl. Heidelberg [u.a.]

European journal of nuclear medicine and molecular imaging 53(10), 5709 - 5720 () [10.1007/s00259-026-07932-0]

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Abstract: [18F]fluorodeprenyl-D2 ([18F]F-DED) positron emission tomography (PET) imaging detects reactive astrogliosis in patients with autoimmune encephalitis (AIE) and multiple system atrophy (MSA). Although dynamic 60-min acquisitions are established, shorter static imaging protocols are desirable for severely impaired patients. This study investigated the feasibility of short static time windows for [18F]F-DED PET imaging in AIE and MSA.Dynamic 60-min [18F]F-DED PET scans were analyzed in 20 patients with AIE, 20 patients with MSA (MSA-P/MSA-C), and 16 controls (CTRL). Disease-related lesions were manually segmented based on visually detectable positive PET-signal in AIE and MSA predilection sites (i.e. mesial temporal lobe, posterior putamen, cerebellar deep white matter), and standardized uptake value ratios (SUVr; cerebellar cortex as a reference tissue) were calculated for consecutive 10-min intervals. Advanced kinetic parameters (DVR, VTr) were derived using Logan plot and a one-tissue compartment model (1TC2k) with image-derived input functions, both applying the cerebellar cortex as a reference tissue.Static images acquired between 10 and 60 min p.i. showed good image contrast and signal-to-noise ratio. SUVr of lesions increased over time and approached a plateau at approximately 50-60 min p.i.. The strongest agreement between SUVr and DVR was observed between 30 and 50 min p.i.. Late-phase SUVr outperformed kinetic parameters in discriminating lesions from healthy tissue in both AIE and MSA.Short static [18F⁸ ]F-DED PET acquisitions are clinically robust for detecting neuroinflammation in AIE and MSA. A late static acquisition between 30-50 min p.i. provides the optimal balance between accuracy and scanning efficiency.

Keyword(s): Humans (MeSH) ; Positron-Emission Tomography: methods (MeSH) ; Female (MeSH) ; Feasibility Studies (MeSH) ; Male (MeSH) ; Multiple System Atrophy: diagnostic imaging (MeSH) ; Middle Aged (MeSH) ; Encephalitis: diagnostic imaging (MeSH) ; Aged (MeSH) ; Time Factors (MeSH) ; Adult (MeSH) ; Hashimoto Disease: diagnostic imaging (MeSH) ; Autoimmune encephalitis ; MAO-B PET ; Multiple system atrophy ; Short imaging window ; [18F]fluordeprenyl-D2

Classification:

Contributing Institute(s):
  1. Molecular Neurodegeneration (AG Haass)
  2. Clinical Research (Munich) (Clinical Research (Munich))
  3. Translational Neurodegeneration (AG Höglinger)
  4. Vascular Cognitive Impairment & Post-Stroke Dementia (AG Dichgans)
  5. Clinical Neurodegeneration (AG Levin)
Research Program(s):
  1. 352 - Disease Mechanisms (POF4-352) (POF4-352)
  2. 353 - Clinical and Health Care Research (POF4-353) (POF4-353)

Database coverage:
Medline ; Clarivate Analytics Master Journal List ; Current Contents - Clinical Medicine ; Current Contents - Life Sciences ; DEAL Springer ; DEAL Springer ; Ebsco Academic Search ; Essential Science Indicators ; IF >= 5 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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The record appears in these collections:
Institute Collections > M DZNE > M DZNE-Clinical Research (Munich)
Document types > Articles > Journal Article
Institute Collections > M DZNE > M DZNE-AG Dichgans
Institute Collections > M DZNE > M DZNE-AG Haass
Institute Collections > M DZNE > M DZNE-AG Levin
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 Record created 2026-07-31, last modified 2026-07-31


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