Non-uniform shrinkage for obtaining computational start shape for in-vivo MRI-based plaque vulnerability assessment

2011 ◽  
Vol 44 (12) ◽  
pp. 2316-2319 ◽  
Author(s):  
Yuan Huang ◽  
Zhongzhao Teng ◽  
Umar Sadat ◽  
Sarah Hilborne ◽  
Victoria E. Young ◽  
...  
2018 ◽  
Vol 39 (suppl_1) ◽  
Author(s):  
S Fiorelli ◽  
S Eligini ◽  
N Cosentino ◽  
F Fabbiocchi ◽  
G Niccoli ◽  
...  

2017 ◽  
Vol 209 (1) ◽  
pp. 142-151 ◽  
Author(s):  
Marie-Hélène Roy Cardinal ◽  
Maarten H. G. Heusinkveld ◽  
Zhao Qin ◽  
Richard G. P. Lopata ◽  
Cyrille Naim ◽  
...  

Author(s):  
Zhongzhao Teng ◽  
Xueying Huang ◽  
Chun Yuan ◽  
Gador Canton ◽  
Fei Liu ◽  
...  

Carotid atherosclerotic plaque (CAP) may rupture without warning and cause acute cardiovascular syndromes such as stroke, which is the No.3 killer in USA and a leading cause of serious disabilities. Available screening and diagnosis techniques are insufficient to identify those victims before the event occurs. Noninvasive methods to identify new and emerging biomarkers to assess plaque vulnerability and predict possible rupture before the fatal event are urgently called for.


Author(s):  
Brigit den Adel ◽  
Mat J. Daemen ◽  
Robert E. Poelmann ◽  
Louise van der Weerd

Recent advances in molecular resonance imaging of atherosclerosis enable to visualize atherosclerotic plaques in vivo using molecular targeted contrast agents. This offers opportunities to study atherosclerosis development and plaque vulnerability noninvasively. In this review, we discuss MRI contrast agents targeted toward atherosclerotic plaques and illustrate how these new imaging platforms could assist in our understanding of atherogenesis and atheroprogression. In particular, we highlight the challenges and limitations of the different contrast agents and hurdles for clinical application. We describe the most promising existing compounds to detect atherosclerosis and plaque vulnerability. Of particular interest are the fibrin-targeted compounds that detect thrombi and, furthermore, the contrast agents targeted to integrins that allow to visualize plaque neovascularization. Moreover, vascular cell adhesion molecule 1–targeted iron oxides seem promising for early detection of atherosclerosis. These targeted MRI contrast agents, however promising and well characterized in (pre)clinical models, lack specificity for plaque vulnerability.


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