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

被引:19
作者
Derlin, Thorsten [1 ]
Spencer, Benjamin A. [2 ]
Mamach, Martin [3 ]
Abdelhafez, Yasser [4 ]
Nardo, Lorenzo [4 ]
Badawi, Ramsey D. [2 ,4 ]
Cherry, Simon R. [2 ,4 ]
Bengel, Frank M. [1 ]
机构
[1] Hannover Med Sch, Dept Nucl Med, Hannover, Germany
[2] Univ Calif Davis, Dept Biomed Engn, Davis, CA USA
[3] Hannover Med Sch, Dept Med Phys & Radiat Protect, Hannover, Germany
[4] Univ Calif Davis, Dept Radiol, Davis, CA USA
基金
美国国家卫生研究院;
关键词
vessel wall; PET; total-body imaging; inflammation; atherosclerosis; INFLAMMATION; PLAQUE; EANM;
D O I
10.2967/jnumed.122.264550
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
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 tech-niques. 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 ves-sel 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 sup-port the feasibility of serial imaging in low-risk populations and will stimulate future mechanistic studies or therapy monitoring in athero-sclerosis and other vessel wall pathologies.
引用
收藏
页码:416 / 422
页数:7
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