Department of Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.
Int J Cardiovasc Imaging. 2010 Apr;26(4):433-45. doi: 10.1007/s10554-009-9565-8. Epub 2010 Jan 29.
Atherosclerotic plaque disruption accounts for the major part of cardiovascular mortality and the risk of disruption appears to depend on plaque composition. Carotid plaques in patients, scheduled for endarterectomy, have been successfully characterised with MRI. MRI has the advantage of combining information about morphology and function. Unfortunately, the tortuosity and size of the coronary arteries, and the respiratory and cardiac motion hinder the in vivo characterisation of human coronary plaque. In addition to plaque composition several molecular markers of the different processes involved in atherosclerosis, such as integrins, matrix metalloproteinases and fibrin seem to correlate with risk of plaque rupture and clinical outcome. These molecular markers can be targeted with antibodies coupled to carriers, which are loaded with gadolinium for detection (molecular MRI). Several cellular/molecular MRI studies in animal models and some in human patients have been conducted with varying levels of success. The advent of clinical high field magnets, the development of contrast agent carriers with high relaxivity and the development of relatively new MR contrast techniques are promising in the field of plaque imaging. Future MRI studies will have to focus on the molecular target of the atherosclerotic process, which has the highest prognostic value with regard to acute coronary syndromes and on the most suitable contrast agent to visualize that target.
动脉粥样硬化斑块破裂是心血管死亡率的主要原因,而破裂的风险似乎取决于斑块的组成。计划进行内膜切除术的患者颈动脉斑块已经可以通过 MRI 成功地进行特征描述。MRI 具有结合形态和功能信息的优势。不幸的是,冠状动脉的迂曲和大小,以及呼吸和心脏运动,阻碍了人体冠状动脉斑块的体内特征描述。除了斑块组成外,几种与动脉粥样硬化不同过程相关的分子标志物,如整合素、基质金属蛋白酶和纤维蛋白,似乎与斑块破裂风险和临床结果相关。这些分子标志物可以用与载体偶联的抗体作为靶点,载体上装载有钆以进行检测(分子 MRI)。已经在动物模型和一些人类患者中进行了几种细胞/分子 MRI 研究,取得了不同程度的成功。临床高磁场的出现、高弛豫率的对比剂载体的开发以及相对较新的磁共振对比技术的发展,为斑块成像领域带来了希望。未来的 MRI 研究将不得不集中在与急性冠状动脉综合征最相关的动脉粥样硬化过程的分子靶点上,以及最适合可视化该靶点的对比剂上。