Cerebral serotonin transporter measurements with [11C]DASB: A review on acquisition and preprocessing across 21 PET centres

Author:

Nørgaard Martin12,Ganz Melanie13,Svarer Claus1,Feng Ling1,Ichise Masanori4,Lanzenberger Rupert5,Lubberink Mark6,Parsey Ramin V7,Politis Marios8,Rabiner Eugenii A910,Slifstein Mark7,Sossi Vesna11,Suhara Tetsuya4,Talbot Peter S12,Turkheimer Federico13,Strother Stephen C14,Knudsen Gitte M12

Affiliation:

1. Neurobiology Research Unit, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark

2. Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark

3. Department of Computer Science, University of Copenhagen, Copenhagen, Denmark

4. Department of Functional Brain Imaging Research, National Institute of Radiological Sciences, National Institutes for Quantum and Radiological Science and Technology, Chiba, Japan

5. Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria

6. Department of Nuclear Medicine and Positron Emission Tomography, Uppsala University, Uppsala, Sweden

7. Department of Psychiatry, School of Medicine, Stony Brook University, Stony Brook, NY, USA

8. Neurodegeneration Imaging Group, Institute of Psychiatry, Psychology and Neuroscience (IoPPN), King's College London, London, UK

9. Imanova Limited, London, UK

10. Centre for Neuroimaging Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK

11. Department of Physics and Astronomy, University of British Columbia, Vancouver, BC, Canada

12. Division of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK

13. Department of Neuroimaging, King's College London, London, UK

14. Rotman Research Institute at Baycrest, University of Toronto, Toronto, Canada

Abstract

Positron Emission Tomography (PET) imaging has become a prominent tool to capture the spatiotemporal distribution of neurotransmitters and receptors in the brain. The outcome of a PET study can, however, potentially be obscured by suboptimal and/or inconsistent choices made in complex processing pipelines required to reach a quantitative estimate of radioligand binding. Variations in subject selection, experimental design, data acquisition, preprocessing, and statistical analysis may lead to different outcomes and neurobiological interpretations. We here review the approaches used in 105 original research articles published by 21 different PET centres, using the tracer [11C]DASB for quantification of cerebral serotonin transporter binding, as an exemplary case. We highlight and quantify the impact of the remarkable variety of ways in which researchers are currently conducting their studies, while implicitly expecting generalizable results across research groups. Our review provides evidence that the foundation for a given choice of a preprocessing pipeline seems to be an overlooked aspect in modern PET neuroscience. Furthermore, we believe that a thorough testing of pipeline performance is necessary to produce reproducible research outcomes, avoiding biased results and allowing for better understanding of human brain function.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Clinical Neurology,Neurology

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