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Gallium-68 labelled RGD PET/CT imaging of endothelial activation in COVID-19 patients
Evelien A J van Genugten1, Theresa J van Lith2, Frederik M A van den Heuvel3
1Department of Medical Imaging, Radboud University Medical Center, Geert Grooteplein Zuid 10, 6525GA, Nijmegen, The Netherlands.
Insights
Positron emission tomography (PET) imaging with gallium-68 labelled RGD-peptide (68Ga-RGD) revealed increased endothelial activation in the lungs and heart of COVID-19 patients. This suggests endothelial cell involvement in the cardiopulmonary system during COVID-19 infection.
Area of Science:
- Cardiovascular Diseases
- Infectious Diseases
- Medical Imaging
Background:
- Endothelial cells are crucial in COVID-19, with dysfunction linked to vascular issues.
- αvβ3 integrin expression on activated endothelial cells can be targeted by 68Ga-RGD for imaging.
Purpose of the Study:
- To investigate endothelial activation in COVID-19 patients using 68Ga-RGD PET/CT.
- To quantify tracer uptake in the lungs, myocardium, and carotid arteries of COVID-19 patients.
Main Methods:
- A prospective observational study included ten hospitalized COVID-19 patients and five controls.
- 68Ga-RGD PET/CT scans were performed, followed by iodine mapping of lung parenchyma.
- Standardized uptake values (SUV) were calculated for lung parenchyma, carotid arteries, and myocardium.
Main Results:
- COVID-19 patients showed significantly increased 68Ga-RGD uptake in the lungs (SUV 0.99±0.32 vs. 0.45±0.18) and myocardium (SUV 3.44±1.59 vs. 0.65±0.22) compared to controls (p<0.01).
- No significant difference in uptake was observed in the carotid arteries.
- Iodine maps indicated perfusion variations but did not correlate with SUV.
Conclusions:
- 68Ga-RGD PET/CT demonstrates increased endothelial activation in the lungs and myocardium of COVID-19 patients.
- These findings highlight the significant role of endothelial cell activation in the cardiopulmonary system during COVID-19.
Abstract:
In coronavirus disease 2019 (COVID-19), endothelial cells play a central role and an inadequate response is associated with vascular complications. PET imaging with gallium-68 labelled RGD-peptide (68Ga-RGD) targets αvβ3 integrin expression which allows quantification of endothelial activation. In this single-center, prospective observational study, we included ten hospitalized patients with COVID-19 between October 2020 and January 2021. Patients underwent 68Ga-RGD PET/CT followed by iodine mapping of lung parenchyma. CT-based segmentation of lung parenchyma, carotid arteries and myocardium was used to quantify tracer uptake by calculating standardized uptake values (SUV). Five non-COVID-19 patients were used as reference. The study population was 68.5 (IQR 52.0-74.5) years old, with median oxygen need of 3 l/min (IQR 0.9-4.0). 68Ga-RGD uptake quantified as SUV ± SD was increased in lungs (0.99 ± 0.32 vs. 0.45 ± 0.18, p < 0.01) and myocardium (3.44 ± 1.59 vs. 0.65 ± 0.22, p < 0.01) of COVID-19 patients compared to reference but not in the carotid arteries. Iodine maps showed local variations in parenchymal perfusion but no correlation with SUV. In conclusion, using 68Ga-RGD PET/CT in COVID-19 patients admitted with respiratory symptoms, we demonstrated increased endothelial activation in the lung parenchyma and myocardium. Our findings indicate the involvement of increased and localized endothelial cell activation in the cardiopulmonary system in COVID-19 patients.Trail registration: NCT04596943.
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