Qualitative and quantitative analysis of 18F-GP1 positron emission tomography in thrombotic cardiovascular disease
Beth Whittington1, Evangelos Tzolos2, Shruti Joshi2
1BHF Centre for Cardiovascular Science, University of Edinburgh, 47 Little France Crescent, Edinburgh, EH16 4TJ, UK. bwhittin@ed.ac.uk.
Insights
This study shows that the novel radiotracer 18F-GP1 has excellent observer repeatability for detecting activated platelets and thrombi in coronary, carotid, and cerebral vessels. These findings support its use in diagnosing conditions like myocardial infarction and ischemic stroke.
Area of Science:
- Nuclear Medicine
- Cardiovascular Imaging
- Neurology
Background:
- Activated platelets and thrombi are key in acute myocardial infarction (AMI) and ischemic stroke.
- Novel radiotracers are needed for precise imaging of these pathological processes.
- 18F-GP1 is a new radiotracer targeting activated platelets and thrombus.
Purpose of the Study:
- To assess the observer repeatability of coronary, carotid, and cerebral 18F-GP1 uptake.
- To evaluate both qualitative and quantitative measurements of 18F-GP1 uptake in patients with AMI or ischemic stroke.
Main Methods:
- Forty-three patients with acute myocardial infarction or ischemic stroke underwent hybrid positron emission tomography (PET) and computed tomography (CT) angiography.
- Qualitative and quantitative assessments of 18F-GP1 uptake were performed on coronary arteries, carotid arteries, and brain parenchyma.
- Intraobserver and interobserver agreement for SUVmax and TBRmax were analyzed.
Main Results:
- Excellent intraobserver and interobserver agreement for qualitative 18F-GP1 uptake (presence/absence).
- Excellent intraobserver repeatability for quantitative SUVmax and TBRmax in all analyzed vascular beds (ICC ≥ 0.92).
- Good interobserver repeatability for quantitative SUVmax and TBRmax (ICC ≥ 0.89), with strongest agreement in brain parenchyma.
Conclusions:
- 18F-GP1 PET-CT imaging demonstrates robust and repeatable qualitative and quantitative measurements.
- The tracer reliably detects activated platelets and thrombi in coronary, carotid, and cerebral vasculature.
- These findings support the clinical utility of 18F-GP1 for diagnosing thrombotic events.
Abstract:
18F-GP1 is a novel highly specific radiotracer that binds to activated platelets and thrombus. We aimed to establish the observer repeatability of coronary, carotid and cerebral 18F-GP1 uptake in patients presenting with acute myocardial infarction or ischaemic stroke. Forty-three patients presenting with acute myocardial infarction or ischaemic stroke underwent hybrid positron emission tomography (PET) and computed tomography (CT) angiography. Qualitative and quantitative assessment of 18F-GP1 uptake was performed on coronary arteries, carotid arteries and brain parenchyma. Qualitative uptake of 18F-GP1 had excellent intraobserver and interobserver agreement, with complete agreement for the presence or absence of visual 18F-GP1 uptake. For quantitative analysis, there were excellent intraclass correlation coefficients for intraobserver repeatability for coronary artery, carotid artery and brain parenchymal SUVmax and TBRmax measurements (all ≥ 0.92). Coronary artery and brain parenchymal analyses showed the strongest agreement in SUVmax values with mean biases of - 0.04 (limits of agreement - 0.21 to 0.20) and 0.02 (limits of agreement - 0.29 to 0.32) respectively. There was good interclass correlation coefficients for interobserver repeatability for coronary artery, carotid artery and brain parenchymal SUVmax and TBRmax measurements (all ≥ 0.89). The strongest interobserver agreement was seen with brain parenchymal SUVmax (mean SUVmax 1.95 ± 0.94) and TBRmax (mean TBRmax 9.55 ± 6.56) with mean biases of - 0.05 (limits of agreement - 0.37 to 0.27) and 0.04 (limits of agreement - 0.59 to 0.52) respectively. Visual qualitative and quantitative 18F-GP1 PET-CT image analyses provide robust and repeatable measurements of activated platelets and thrombi within the coronary arteries, carotid arteries and brain parenchyma.
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