Abstract

Positron emission tomography (PET) is a non-invasive molecular imaging technique using positron-emitting radioisotopes to study functional processes within the body. High resolution PET scanners designed for imaging rodents and non-human primates are now commonplace in preclinical research. Brain imaging in this context, with motion compensation, can potentially enhance the usefulness of PET by avoiding confounds due to anaesthetic drugs and enabling freely moving animals to be imaged during normal and evoked behaviours. Due to the frequent and rapid motion exhibited by alert, awake animals, optimal motion correction requires frequently sampled pose information and precise synchronisation of these data with events in the PET coincidence data stream. Motion measurements should also be as accurate as possible to avoid degrading the excellent spatial resolution provided by state-of-the-art scanners. Here we describe and validate methods for optimised motion tracking suited to the correction of motion in awake rats. A hardware based synchronisation approach is used to achieve temporal alignment of tracker and scanner data to within 10 ms. We explored the impact of motion tracker synchronisation error, pose sampling rate, rate of motion, and marker size on motion correction accuracy. With accurate synchronisation (<100 ms error), a sampling rate of >20 Hz, and a small head marker suitable for awake animal studies, excellent motion correction results were obtained in phantom studies with a variety of continuous motion patterns, including realistic rat motion (<5% bias in mean concentration). Feasibility of the approach was also demonstrated in an awake rat study. We conclude that motion tracking parameters needed for effective motion correction in preclinical brain imaging of awake rats are achievable in the laboratory setting. This could broaden the scope of animal experiments currently possible with PET.

Highlights

  • Positron emission tomography (PET) is a non-invasive imaging technique that uses positron-emitting radioisotopes to study functional processes within the body

  • Small animal PET, characterised by smaller scanner bore size and crystal size, and higher spatial resolution compared with human PET, plays a key role in preclinical research based on animal models

  • Our results demonstrate the relative impact of these various factors, and indicate that motion tracking parameters needed for effective motion correction in preclinical brain imaging of awake rats are achievable in the laboratory setting

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Summary

Introduction

Positron emission tomography (PET) is a non-invasive imaging technique that uses positron-emitting radioisotopes to study functional processes within the body. PET measurements provide information about the spatial distribution and expression levels of specific cellular targets such as receptors or enzymes. Changes in functional activity due to physiological, pathological or pharmacological challenges are readily measured. Small animal PET, characterised by smaller scanner bore size and crystal size, and higher spatial resolution compared with human PET, plays a key role in preclinical research based on animal models. The ability to perform longitudinal studies in the same animal is useful [1]. A comprehensive description of PET physics, instrumentation and methodology can be found in [2]

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