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

被引:32
|
作者
Garcia-Lorenzo, Daniel [1 ]
Lavisse, Sonia [2 ,3 ]
Leroy, Claire [4 ,5 ]
Wimberley, Catriona [4 ,5 ]
Bodini, Benedetta [1 ]
Remy, Philippe [2 ,3 ,7 ,8 ]
Veronese, Mattia [6 ]
Turkheimer, Federico [6 ]
Stankoff, Bruno [1 ,9 ]
Bottlaender, Michel [4 ,5 ,10 ]
机构
[1] Sorbonne Univ, UPMC Paris 6, Hop Pitie Salpetriere, Inst Cerveau & Moelle Epiniere,ICM, Paris, France
[2] Commissariat Energie Atom & Energies Alternat CEA, Inst Imagerie Biomed I2BM, DRF, MIRCen, Fontenay Aux Roses, France
[3] Univ Paris Saclay, Univ Paris Sud, CNRS, Neurodegenerat Dis Lab, Fontenay Aux Roses, France
[4] Commissariat Energie Atom & Energies Alternat CEA, Inst Imagerie Biomed I2BM, DRF, Serv Hosp Frederic Joliot, Orsay, France
[5] Univ Paris Saclay, Univ Paris Sud, CNRS, INSERM,CEA,IMIV, Orsay, France
[6] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Neuroimaging, London, England
[7] CHU Henri Mondor, AP HP, Ctr Expert Parkinson, Neurol, Creteil, France
[8] Univ Paris Est, Creteil, France
[9] Hop St Antoine, AP HP, Paris, France
[10] Commissariat Energie Atom & Energies Alternat CEA, UNIACT, Inst Imagerie Biomed I2BM, DRF,Neurospin, Gif Sur Yvette, France
来源
关键词
Inflammation; microglia; positron emission tomography; brain imaging and clinical trials; POSITRON-EMISSION-TOMOGRAPHY; PROTEIN; 18; KDA; BENZODIAZEPINE BINDING-SITES; TRANSLOCATOR PROTEIN; ALZHEIMERS-DISEASE; MICROGLIAL ACTIVATION; GENETIC-POLYMORPHISM; RADIOLIGAND BINDING; HEALTHY CONTROLS; WHITE-MATTER;
D O I
10.1177/0271678X17692599
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There is a great need for a non-invasive methodology enabling the quantification of translocator protein overexpression in PET clinical imaging. [(18) F] 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 [18 F] DPA-714 analysis. Fourteen healthy subjects genotyped for translocator protein underwent an [(18) F] DPA-714 PET, including 10 with metabolite-corrected arterial input function and three for a test-retest assessment. Two-tissue compartmental modelling provided BPND (AIF) estimates that were compared to either BPNDLoganSCA or BPND (LoganCRB) 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. BPND (AIF,) BPNDLoganSCA and BPND (LoganCRB) were highly correlated (ICC of 0.91 +/- 0.05) but BPND (LoganSCA) were similar to 26% higher and less variable than BPND (LoganCRB) . Reproducibility was good with 5% variability in the test-retest study. The clustering technique for [(18) F] DPA-714 provides a simple, robust and reproducible technique that can be used for all neurological diseases.
引用
收藏
页码:333 / 346
页数:14
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