Sophisticated Prediction of Carotid-Plaque Vulnerability by Nanocluster Sensitized Vessel-Wall-Imaging Profile in Rabbit

OBJECTIVETo innovatively developed a macrophage-target nanoparticle based contrast-enhanced high-resolution magnetic resonance vessel wall imaging (HR-VWI) strategy to characterize the plaques vulnerable features on rabbits. BACKGROUNDLacking of sensitive and specific image-marker of HR-VWI leads this technique depending upon the plaque morphological characteristics. Nanoparticle-based contrast agents modified with targeting ligands allow amplifying MR signals of the interested components. The key to successful translation is the requirement that conducting studies in larger animals to provide reasonable diagnostic readouts. METHODSThe HR-VWI enhanced with macrophage-targeted PP1-Au@GSH@Gd (GdMG) nanoclusters (NCs) and the conventional Gadovist were utilized for the plaque vulnerability evaluation by a systematic histogram analysis in atherosclerosis (AS) rabbit model. RESULTSDue to the compelling targeting capacity of GdMG NCs to foamy macrophages, the contrast-to-noise ratio (CNR) from pre-injection baseline dramatically raised from 6.50 to 36.91 (p < 0.001), with an increment of 1.39-fold higher than that of the Gadovist approach. Spearman s correlation test confirmed that the coefficient of variation (CV) derived from the histogram analysis based on GdMG NCs HR-VWI was indeed positively linearly correlated with pathology vulnerability index (VIP) significantly (p < 0.05) with adjusted R2 = 0.775. Finally, mathematic formulas with histogram-derived parameters as variables were fitted to quantitatively calculate the histogram vulnerability index (VIH) with the strength of the adjusted R2 = 0.952 (p < 0.001), and Area under the curve (AUC) of 0.875 (p < 0.001) to realize the in vivo and quantitative calculation of the plaque vulnerability. CONCLUSIONProfiting from the splendid inflammation targeted capacity and excellent MRI performance of GdMG NCs, as well as the highly quantitative characteristics of histogram analysis, we disclosed that our established imaging protocol was able to identify the plaques vulnerability index that were comparable to pathological examinations in both retrospective and prospective experiments.