Published in:
01-11-2013 | Original Article
Feasibility and kinetic characteristics of 68Ga-NOTA-RGD PET for in vivo atherosclerosis imaging
Authors:
Jin Chul Paeng, Yun-Sang Lee, Jae Sung Lee, Jae Min Jeong, Ki-Bong Kim, June-Key Chung, Dong Soo Lee
Published in:
Annals of Nuclear Medicine
|
Issue 9/2013
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Abstract
Objective
In this study, the feasibility and kinetic characteristics of the 68Ga-NOTA-RGD, a recently developed RGD peptide agent, were investigated for atherosclerosis imaging in comparison with 18FDG.
Methods
ApoE−/− mice were fed a high-fat diet for more than 20 weeks. To evaluate the feasibility, tissue uptakes of 68Ga-NOTA-RGD and 18FDG in the major organs were measured and compared between ApoE−/− and control mice. Animal PET imaging was also performed and relative uptake values in the thoracic aorta were compared between ApoE−/− and control mice. In humans, the kinetic characteristics and feasibility of 68Ga-NOTA-RGD PET were assessed in 4 patients with known coronary artery disease.
Results
In the tissue uptake study, the thoracic aorta showed higher uptake in ApoE−/− than in control mice with both 68Ga-NOTA-RGD and 18FDG (P < 0.001). On PET scans, the relative uptake values of the thoracic aorta were significantly higher in ApoE−/− with both 68Ga-NOTA-RGD (P = 0.024) and 18FDG (P = 0.038). In human PET, the appropriateness of reversible binding model and Logan plotting was clearly demonstrated. The aorta-to-jugular ratios were measured up to 1.25 and showed a tendency to correlate with the serum high-sensitivity C-reactive protein level (r = 0.899, P = 0.102).
Conclusions
68Ga-NOTA-RGD has potential as an in vivo atherosclerosis imaging agent. However, the lower imaging contrast and sensitivity of 68Ga-NOTA-RGD PET compared with 18FDG PET may be a limitation for clinical application.