Characterization of coronary atherosclerotic plaque using multicontrast MRI acquired under simulated in vivo conditions.
Characterization of coronary atherosclerotic plaque using multicontrast MRI acquired under simulated in vivo conditions.
复制标题
使用在模拟体内条件下获得的多重对比 MRI 表征冠状动脉粥样硬化斑块。
DOI:
10.1002/jmri.20687
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发表时间:
2006
期刊:
影响因子:
--
通讯作者:
Oshinski,JohnN
中科院分区:
文献类型:
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作者:
Sun,Binjian;Giddens,DonP;LongJr,Robert;Taylor,WRobert;Weiss,Diana;Joseph,Giji;Vega,David;Oshinski,JohnN
PurposeTo compare coronary atherosclerotic plaque characterization using multicontrast MRI on: 1) freshly excised vessels under simulated in vivo conditions, and 2) preserved vessels.Materials and MethodsT1‐weighted (T1W), T2‐weighted (T2W), proton density‐weighted (PDW), and diffusion‐weighted (DW) MR images were acquired on 13 freshly excised human coronary arteries from explanted hearts. Vessels were imaged in an MR‐compatible tissue culture chamber using a 4.7 Tesla small‐bore MR scanner. Eight vessels were then preserved in buffered formalin and rescanned following the same imaging protocol. A three‐dimensional spatially penalized fuzzy C‐means (3D‐SPFCM) technique was applied to classify different plaque constituents. The classification results from vessels under “fresh” and “preserved” conditions were compared with corresponding histological sections.ResultsFor most plaque constituents, the plaque characterization results show no significant difference between fresh and preserved scans, and little difference between scans and the histological reference standard. In the case of thrombus, apparent signal changes between fresh and preserved images were identified. Overall, MR scans conducted under preserved conditions provided a 1.8% to 17.5% greater signal‐to‐noise ratio (SNR) than those conducted in the fresh stage.ConclusionPreservation of coronary vessels did not alter the contrast between plaque tissues on multicontrast MRI, and did not significantly change the results of plaque constituent characterization. J. Magn. Reson. Imaging 2006. © 2006 Wiley‐Liss, Inc.