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Research ArticleClinical Investigation

Exploring Vessel Wall Biology In Vivo by Ultrasensitive Total-Body PET

Thorsten Derlin, Benjamin A. Spencer, Martin Mamach, Yasser Abdelhafez, Lorenzo Nardo, Ramsey D. Badawi, Simon R. Cherry and Frank M. Bengel
Journal of Nuclear Medicine March 2023, 64 (3) 416-422; DOI: https://doi.org/10.2967/jnumed.122.264550
Thorsten Derlin
1Department of Nuclear Medicine, Hannover Medical School, Hannover, Germany;
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Benjamin A. Spencer
2Department of Biomedical Engineering, University of California, Davis, Davis, California;
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Martin Mamach
3Department of Medical Physics and Radiation Protection, Hannover Medical School, Hannover, Germany; and
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Yasser Abdelhafez
4Department of Radiology, University of California, Davis, Davis, California
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Lorenzo Nardo
4Department of Radiology, University of California, Davis, Davis, California
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Ramsey D. Badawi
2Department of Biomedical Engineering, University of California, Davis, Davis, California;
4Department of Radiology, University of California, Davis, Davis, California
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Simon R. Cherry
2Department of Biomedical Engineering, University of California, Davis, Davis, California;
4Department of Radiology, University of California, Davis, Davis, California
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Frank M. Bengel
1Department of Nuclear Medicine, Hannover Medical School, Hannover, Germany;
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Abstract

Ultrasensitive, high-resolution, extended-field-of-view total-body (TB) PET using the first-of-its-kind 194-cm axial-field-of-view uEXPLORER may facilitate the interrogation of biologic hallmarks of hitherto difficult-to-evaluate low-signal vessel wall pathology in cardiovascular disease. Methods: Healthy volunteers were imaged serially for up to 12 h after a standard dose of 18F-FDG (n = 15) or for up to 3 h after injection of a very low dose (about 5% of a standard dose; n = 15). A cohort undergoing standard 18F-FDG PET (n = 15) on a conventional scanner with a 22-cm axial field of view served as a comparison group. Arterial wall signal, crosstalk with hematopoietic and lymphoid organs, and image quality were analyzed using standardized techniques. Results: TB PET depicted the large vessel walls with excellent quality. The arterial wall could be imaged with high contrast up to 12 h after tracer injection. Ultralow-dose TB 18F-FDG images yielded a vessel wall signal and target-to-background ratio comparable to those of conventional-dose, short-axial-field-of-view PET. Crosstalk between vessel wall and lymphoid organs was identified with better accuracy in both TB PET cohorts than in conventional PET. Conclusion: TB PET enables detailed assessment of in vivo vessel wall biology and its crosstalk with other organs over an extended time window after tracer injection or at an ultralow tracer dose. These initial observations support the feasibility of serial imaging in low-risk populations and will stimulate future mechanistic studies or therapy monitoring in atherosclerosis and other vessel wall pathologies.

  • vessel wall
  • PET
  • total-body imaging
  • inflammation
  • atherosclerosis

Footnotes

  • Published online Sep. 29, 2022.

  • © 2023 by the Society of Nuclear Medicine and Molecular Imaging.
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Journal of Nuclear Medicine: 64 (3)
Journal of Nuclear Medicine
Vol. 64, Issue 3
March 1, 2023
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Exploring Vessel Wall Biology In Vivo by Ultrasensitive Total-Body PET
Thorsten Derlin, Benjamin A. Spencer, Martin Mamach, Yasser Abdelhafez, Lorenzo Nardo, Ramsey D. Badawi, Simon R. Cherry, Frank M. Bengel
Journal of Nuclear Medicine Mar 2023, 64 (3) 416-422; DOI: 10.2967/jnumed.122.264550

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Exploring Vessel Wall Biology In Vivo by Ultrasensitive Total-Body PET
Thorsten Derlin, Benjamin A. Spencer, Martin Mamach, Yasser Abdelhafez, Lorenzo Nardo, Ramsey D. Badawi, Simon R. Cherry, Frank M. Bengel
Journal of Nuclear Medicine Mar 2023, 64 (3) 416-422; DOI: 10.2967/jnumed.122.264550
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Keywords

  • Vessel Wall
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  • inflammation
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