Innovative atherosclerosis imaging using 18F-NaF PET/CT: Its clinical potential
Innovative atherosclerosis imaging using 18F-NaF PET/CT: Its clinical potential
复制标题
使用 18F-NaF PET/CT 的创新动脉粥样硬化成像:其临床潜力
DOI:
10.1007/s12350-021-02576-z
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发表时间:
2021
影响因子:
2.4
通讯作者:
Yukiko Nakano
中科院分区:
文献类型:
--
作者:
T. Kitagawa;Yukiko Nakano
Atherosclerosis is a major cause of critical cardiovascular disorders, including myocardial infarction, stroke, and peripheral arterial disease. F-sodium fluoride (F-NaF) positron emission tomography (PET) has recently gained attention in the field of cardiovascular diseases and data have shown its usefulness in identifying high-risk atherosclerotic lesions with active calcification. Lee et al. demonstrated that coronary plaques with high-risk characteristics on intravascular imaging (intravascular ultrasound and optical coherence tomography) had higher F-NaF uptake than those without such characteristics. Kitagawa et al. assessed the relationship between the F-NaF signal on PET and the appearance of coronary atherosclerosis on cardiac computed tomography (CT) examination and found the following: (1) The coronary calcium score was positively correlated with coronary arterial F-NaF uptake per patient; (2) patients with a history of myocardial infarction or unstable angina had higher coronary arterial F-NaF uptake; (3) focally increased F-NaF uptake in coronary atherosclerosis was independently correlated with the heterogeneous (partially calcified) plaque component; and (4) coronary plaques with highrisk features on coronary CT angiography (CCTA) had a higher F-NaF uptake on PET than those without. In addition, intense F-NaF uptake was shown in recently ruptured coronary plaques in patients with acute myocardial infarction. These points highlight the potential of F-NaF PET imaging as an innovative approach to monitoring atherosclerosis. Why does F-NaF uptake indicate ruptured or high-risk atherosclerotic plaques? The F-NaF tracer reacts with hydroxyapatite, which is the central component of vascular calcification and is deposited during the earliest and most active stages of mineralization. Atherosclerotic calcification is described as a cellular response to acute and chronic inflammatory stimuli, and the association between osteogenesis and inflammation in atherosclerosis is well described. Therefore, atherosclerotic inflammation precedes vascular calcification, and the presence of microcalcifications are associated with inflammatory cell infiltrate that coexists with other high-risk features of atherosclerotic plaque, including a large lipid core, outward remodeling, and thin fibrous cap. F-NaF uptake is thus a comprehensive imaging marker of high-risk atherosclerotic plaques (Figure 1). In imaging of coronary arteries, F-NaF tracer, unlike F-fluorodeoxyglucose (F-FDG), is not taken up physiologically in the myocardium; therefore, coronary atherosclerotic lesions can be specifically detected and assessed using F-NaF PET/CT. Fiz et al. conducted an interesting analysis on the correlation between F-NaF uptake in the vessel walls and a successive increase in the calcium burden. They focused on (1) the significance of F-NaF uptake with regard to the CT density of noncalcified arterial lesions and new occurrence of calcification, (2) the significance of F-NaF uptake with regard to subsequent calcified plaque progression represented by CT density and calcium score, and (3) the significance of F-NaF uptake in the whole aorta with regard to the increase in calcium burden. Patients who underwent two consecutive FNaF PET/CT scans were enrolled in their study, and lesions on the abdominal aorta were evaluated. They found that in noncalcified arterial walls, F-NaF uptake is colocalized with an increased CT density and related Reprint requests: Toshiro Kitagawa, MD, PhD, Department of Cardiovascular Medicine, Hiroshima University Graduate School of Biomedical and Health Sciences, 1-2-3 Kasumi, Minami-ku, Hiroshima734-8551, Japan; toshirok@hiroshima-u.ac.jp J Nucl Cardiol 2022;29:1724–8. 1071-3581/$34.00 Copyright 2021 American Society of Nuclear Cardiology.
影响因子:
14
作者:
Kwiecinski, Jacek;Dey, Damini;Berman, Daniel S.
通讯作者:
Berman, Daniel S.
影响因子:
24
作者:
Kwiecinski, Jacek;Tzolos, Evangelos;Dweck, Marc R.
通讯作者:
Dweck, Marc R.