Validation of an automatic reference region extraction for the quantification of [18F]DPA-714 in dynamic brain PET studies

Author:

García-Lorenzo Daniel1,Lavisse Sonia23,Leroy Claire45,Wimberley Catriona45,Bodini Benedetta1,Remy Philippe236,Veronese Mattia7,Turkheimer Federico7,Stankoff Bruno18,Bottlaender Michel459

Affiliation:

1. Sorbonne Université, UPMC Paris 06, Institut du Cerveau et de la Moelle Epinière, ICM, Hôpital de la Pitié Salpêtrière, Paris, France

2. Commissariat à l'Energie Atomique et aux Energies Alternatives (CEA), Département de Recherche Fondamentale (DRF), Institut d'Imagerie Biomédicale (I2BM), MIRCen, Fontenay-aux-Roses, France

3. Centre National de la Recherche Scientifique (CNRS), Université Paris-Sud, Université Paris-Saclay, Neurodegenerative Diseases Laboratory, Fontenay-aux-Roses, France

4. Commissariat à l'Energie Atomique et aux Energies Alternatives (CEA), Département de Recherche Fondamentale (DRF), Institut d'Imagerie Biomédicale (I2BM), Service Hospitalier Frédéric Joliot, Orsay, France

5. Imagerie Moléculaire in Vivo, IMIV, CEA, Inserm, CNRS, Univ. Paris-Sud, Université Paris Saclay, Orsay, France

6. Centre Expert Parkinson, Neurologie, CHU Henri Mondor, Assistance Publique Hôpitaux de Paris and Université Paris-Est, Créteil, France

7. Department of Neuroimaging, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK

8. Hôpital Saint Antoine, AP-HP, Paris, France

9. Commissariat à l'Energie Atomique et aux Energies Alternatives (CEA), Département de Recherche Fondamentale (DRF), Institut d'Imagerie Biomédicale (I2BM),Neurospin, UNIACT, Gif-sur-Yvette, France

Abstract

There is a great need for a non-invasive methodology enabling the quantification of translocator protein overexpression in PET clinical imaging. [18F]DPA-714 has emerged as a promising translocator protein radiotracer as it is fluorinated, highly specific and returned reliable quantification using arterial input function. Cerebellum gray matter was proposed as reference region for simplified quantification; however, this method cannot be used when inflammation involves cerebellum. Here we adapted and validated a supervised clustering (supervised clustering algorithm (SCA)) for [18F]DPA-714 analysis. Fourteen healthy subjects genotyped for translocator protein underwent an [18F]DPA-714 PET, including 10 with metabolite-corrected arterial input function and three for a test–retest assessment. Two-tissue compartmental modelling provided [Formula: see text] estimates that were compared to either [Formula: see text] or [Formula: see text] generated by Logan analysis (using supervised clustering algorithm extracted reference region or cerebellum gray matter). The supervised clustering algorithm successfully extracted a pseudo-reference region with similar reliability using classes that were defined using either all subjects, or separated into HAB and MAB subjects. [Formula: see text], [Formula: see text] and [Formula: see text] were highly correlated (ICC of 0.91 ± 0.05) but [Formula: see text] were ∼26% higher and less variable than [Formula: see text]. Reproducibility was good with 5% variability in the test–retest study. The clustering technique for [18F]DPA-714 provides a simple, robust and reproducible technique that can be used for all neurological diseases.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical),Neurology

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