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Association Between Osteogenesis and Inflammation During the Progression of Calcified Plaque Evaluated by <sup>18</sup>F-Fluoride and <sup>18</sup>F-FDG

47

Citations

25

References

2017

Year

Abstract

<sup>18</sup>F-FDG is the most widely validated PET tracer for the evaluation of atherosclerotic inflammation. Recently, <sup>18</sup>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. <b>Methods:</b> Thirty-four myeloma patients underwent <sup>18</sup>F-NaF and <sup>18</sup>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. <b>Results:</b> There were significant correlations between the maximum tissue-to-background ratios of the 2 tracers (Spearman <i>r</i> = 0.5 [<i>P</i> < 0.01]; Pearson <i>r</i> = 0.4 [<i>P</i> < 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 <i>r</i> = 0.06; <i>P</i> = 0.76). Compared with noncalcified plaques, mildly calcified plaques showed concordant significantly lower accumulation, with good correlation between the tracers (Pearson <i>r</i> = 0.7; <i>P</i> < 0.01). In addition, enhanced osteogenesis-derived <sup>18</sup>F-NaF uptake and regressive inflammation-derived <sup>18</sup>F-FDG uptake were observed in severely calcified lesions (Pearson <i>r</i> = 0.4; <i>P</i> < 0.01). During follow-up, increased calcium density and increased mean <sup>18</sup>F-NaF uptake were observed, whereas mean <sup>18</sup>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. <b>Conclusion:</b> The combination of <sup>18</sup>F-NaF PET imaging and <sup>18</sup>F-FDG PET imaging promotes an understanding of the mechanism of plaque progression, thereby providing new insights into plaque stabilization.

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