Nuclear Imaging Focus on Vascular Probes

被引:8
作者
Hyafil, Fabien [1 ,2 ]
Vigne, Jonathan [2 ,3 ]
机构
[1] Univ Paris 7 Rene Diderot, Bichat Univ Hosp, AP HP, Dept Nucl Med, Paris, France
[2] Univ Paris 7 Rene Diderot, INSERM, U1148, Lab Vasc Translat Sci,DHU,FIRE, Paris, France
[3] Normandie Univ, CHU Caen Normandie, Dept Nucl Med, UNICAEN, Caen, France
关键词
humans; inflammation; nuclear medicine; positron emission tomography; radionuclide imaging; EMISSION TOMOGRAPHY/COMPUTED TOMOGRAPHY; CAROTID PLAQUE INFLAMMATION; ATHEROSCLEROTIC PLAQUES; ARTERIAL INFLAMMATION; MYOCARDIAL-INFARCTION; CARDIOVASCULAR-DISEASE; NONINVASIVE DETECTION; VULNERABLE PLAQUE; F-18-FDG PET/CT; RISK-FACTORS;
D O I
10.1161/ATVBAHA.119.312586
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Noninvasive imaging technologies offer to identify several anatomic and molecular features of high-risk plaques. For the noninvasive molecular imaging of atherosclerotic plaques, nuclear medicine constitutes one of the best imaging modalities, thanks to its high sensitivity for the detection of probes in tissues. 18F-fluorodeoxyglucose (FDG) is currently the most widely used radiopharmaceutical for molecular imaging of atherosclerotic plaques with positron emission tomography. The intensity of FDG uptake in the vascular wall correlates closely with the degree of macrophage infiltration in atherosclerotic plaques. FDG positron emission tomographic imaging has become a powerful tool to identify and monitor noninvasively inflammatory activities in atherosclerotic plaques over time. This review examines how FDG positron emission tomographic imaging has given us deeper insight into the role of inflammation in atherosclerotic plaque progression and discusses perspectives for alternative radiopharmaceuticals to FDG that could provide a more specific and simple identification of high-risk lesions and help improve risk stratification of atherosclerotic patients.
引用
收藏
页码:1369 / 1378
页数:10
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