F-FDG is the most widely validated PET tracer for the evaluation of atherosclerotic inflammation. Recently, F-NaF has also been considered a potential novel biomarker of osteogenesis in atherosclerosis. We aimed to analyze the association between inflammation and osteogenesis at different stages of atherosclerosis, as well as the interrelationship between these 2 processes during disease progression. Thirty-four myeloma patients underwent F-NaF and F-FDG PET/CT examinations. Lesions were divided into 3 groups (noncalcified, mildly calcified, and severely calcified lesions) on the basis of calcium density as measured in Hounsfield units by CT. Tissue-to-background ratios were determined from PET for both tracers. The association between inflammation and osteogenesis during atherosclerosis progression was evaluated in 19 patients who had at least 2 examinations with both tracers. There were significant correlations between the maximum tissue-to-background ratios of the 2 tracers (Spearman = 0.5 [ < 0.01]; Pearson = 0.4 [ < 0.01]) in the 221 lesions at baseline. The highest uptake of both tracers was observed in noncalcified lesions, but without any correlation between the tracers (Pearson = 0.06; = 0.76). Compared with noncalcified plaques, mildly calcified plaques showed concordant significantly lower accumulation, with good correlation between the tracers (Pearson = 0.7; < 0.01). In addition, enhanced osteogenesis-derived F-NaF uptake and regressive inflammation-derived F-FDG uptake were observed in severely calcified lesions (Pearson = 0.4; < 0.01). During follow-up, increased calcium density and increased mean F-NaF uptake were observed, whereas mean F-FDG uptake decreased. Most noncalcified (86%) and mildly calcified (81%) lesions and 47% of severely calcified lesions had concordant development of both vascular inflammation and osteogenesis. The combination of F-NaF PET imaging and F-FDG PET imaging promotes an understanding of the mechanism of plaque progression, thereby providing new insights into plaque stabilization.
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http://dx.doi.org/10.2967/jnumed.116.182790 | DOI Listing |
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