Botnar R M, Ebersberger H, Noerenberg D, Jansen C H P, Wiethoff A J, Schuster A, Kasner M, Walter T C, Knobloch G, Hoppe P, Diederichs G, Hamm B, Makowski M R
Imaging Sciences, King's College London BHF Centre, Division of Imaging Science, Biomedical Research Centre of Guy's and St. Thomas' NHS Foundation Trust, London, UK, London.
Heart Center Munich-Bogenhausen, Munich, Germany, Department of Cardiology and Intensive Care Medicine, Munich.
Rofo. 2015 May;36(2):92-101. doi: 10.1055/s-0034-1385451. Epub 2015 Jan 13.
Cardiovascular diseases remain the leading cause of morbidity and mortality in industrialized and developing countries. In clinical practice, the in-vivo identification of atherosclerotic lesions, which can lead to complications such as heart attack or stroke, remains difficult. Imaging techniques provide the reference standard for the detection of clinically significant atherosclerotic changes in the coronary and carotid arteries. The assessment of the luminal narrowing is feasible, while the differentiation of stable and potentially unstable or vulnerable atherosclerotic plaques is currently not possible using non-invasive imaging. With high spatial resolution and high soft tissue contrast, magnetic resonance imaging (MRI) is a suitable method for the evaluation of the thin arterial wall. In clinical practice, native MRI of the vessel wall already allows the differentiation and characterization of components of atherosclerotic plaques in the carotid arteries and the aorta. Additional diagnostic information can be gained by the use of non-specific MRI contrast agents. With the development of targeted molecular probes, that highlight specific molecules or cells, pathological processes can be visualized at a molecular level with high spatial resolution. In this review article, the development of pathophysiological changes leading to the development of the arterial wall are introduced and discussed. Additionally, principles of contrast enhanced imaging with non-specific contrast agents and molecular probes will be discussed and latest developments in the field of molecular imaging of the vascular wall will be introduced.
Molecular magnetic resonance imaging has great potential to improve the in vivo characterization of atherosclerotic plaques. Based on the molecular information is feasible to enable a better differentiation of stable and unstable (vulnerable) atherosclerotic plaques.
在工业化国家和发展中国家,心血管疾病仍然是发病和死亡的主要原因。在临床实践中,体内识别可能导致心脏病发作或中风等并发症的动脉粥样硬化病变仍然很困难。成像技术为检测冠状动脉和颈动脉临床上显著的动脉粥样硬化变化提供了参考标准。评估管腔狭窄是可行的,而目前使用非侵入性成像无法区分稳定的和潜在不稳定或易损的动脉粥样硬化斑块。磁共振成像(MRI)具有高空间分辨率和高软组织对比度,是评估薄动脉壁的合适方法。在临床实践中,血管壁的原生MRI已经能够区分和表征颈动脉和主动脉中动脉粥样硬化斑块的成分。使用非特异性MRI造影剂可以获得额外的诊断信息。随着靶向分子探针的发展,这些探针可以突出特定分子或细胞,病理过程可以在分子水平上以高空间分辨率可视化。在这篇综述文章中,介绍并讨论了导致动脉壁病变发展的病理生理变化。此外,还将讨论使用非特异性造影剂和分子探针进行对比增强成像的原理,并介绍血管壁分子成像领域的最新进展。
分子磁共振成像在改善动脉粥样硬化斑块的体内表征方面具有巨大潜力。基于分子信息,能够更好地区分稳定和不稳定(易损)的动脉粥样硬化斑块。