Analysis of 18F-Sodium Fluoride Positron Emission Tomography Signal Sources in Atherosclerotic Minipigs Shows Specific Binding of 18F-Sodium Fluoride to Plaque Calcifications
Objective: F-18-sodium fluoride (F-18-NaF) positron emission tomography (PET) imaging is thought to visualize active atherosclerotic plaque calcification. This is supported by the binding of F-18-NaF to plaque calcification ex vivo, but no prior studies have examined binding of F-18-NaF to human-like plaque in vivo. Our aim was to validate the specificity of F-18-NaF PET for plaque calcifications in atherosclerotic minipigs. Approach and Results: Gain-of-function PCSK9(D374Y) (proprotein convertase/subtilisin kexin type 9) transgenic Yucatan minipigs (n=4) were fed high-fat diet for 2.5 years to develop atherosclerosis and then subjected to F-18-NaF PET/computed tomography imaging. The heart, aorta, and iliac arteries were immediately re-scanned ex vivo after surgical extraction. Lesions from the abdominal aorta, iliac arteries, and coronary arteries were cryo-sectioned for autoradiography. Histological plaque characteristics, PET/computed tomography signal, and autoradiography were linked through regression and co-localization analysis. Arterial F-18-NaF PET signal had intensities comparable to clinical scans and colocalized moderately with calcification detected by computed tomography. Histological analysis showed calcification spanning from microcalcifications near lipid pools and necrotic core to more homogenous macrocalcifications. Comparison with arteries from autopsy cases confirmed the resemblance in localization and appearance with early human plaque calcification. Regression analysis in the abdominal aorta showed correlations with calcified plaque but could not rule out contributions from noncalcified plaque. This was resolved by autoradiography, which showed specific accumulation in plaque calcifications in all examined arteries. In the context of porcine abdominal aorta, F-18-NaF PET imaging was, however, less accurate than computed tomography for detecting small calcifications. Conclusions: F-18-NaF accumulates specifically in calcifications of atherosclerotic plaques in vivo.
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Show Chwan Mem Hosp, Dept Neurol, Lukang Township, Changhua County, TaiwanShow Chwan Mem Hosp, Dept Neurol, Lukang Township, Changhua County, Taiwan
Chang, W. L.
Wei, C. Y.
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Show Chwan Mem Hosp, Dept Neurol, Lukang Township, Changhua County, TaiwanShow Chwan Mem Hosp, Dept Neurol, Lukang Township, Changhua County, Taiwan
Wei, C. Y.
Hung, G. U.
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Chang Bing Show Chwan Mem Hosp, Dept Nucl Med, Lukang Township, Changhua County, TaiwanShow Chwan Mem Hosp, Dept Neurol, Lukang Township, Changhua County, Taiwan
Hung, G. U.
Kao, C. H.
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China Med Univ Hosp, Dept Nucl Med, Taichung, TaiwanShow Chwan Mem Hosp, Dept Neurol, Lukang Township, Changhua County, Taiwan
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Princess Alexandra Hosp, Dept Cardiol, Woolloongabba, Qld, Australia
Univ New South Wales, South Western Sydney Clin Sch, Fac Med, Kensington, NSW, AustraliaPrincess Alexandra Hosp, Dept Cardiol, Woolloongabba, Qld, Australia
Ng, Arnold C. T.
van Rosendael, Alexander R.
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Leiden Univ, Med Ctr, Dept Cardiol, Leiden, NetherlandsPrincess Alexandra Hosp, Dept Cardiol, Woolloongabba, Qld, Australia
van Rosendael, Alexander R.
Bax, Jeroen J.
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Leiden Univ, Med Ctr, Dept Cardiol, Leiden, NetherlandsPrincess Alexandra Hosp, Dept Cardiol, Woolloongabba, Qld, Australia