Massachusetts General Hospital, Cardiovascular Research Center and Cardiology Division, Boston, Massachusetts 02114, USA.
J Biomed Opt. 2010 Jan-Feb;15(1):011107. doi: 10.1117/1.3280282.
New imaging methods are urgently needed to identify high-risk atherosclerotic lesions prior to the onset of myocardial infarction, stroke, and ischemic limbs. Molecular imaging offers a new approach to visualize key biological features that characterize high-risk plaques associated with cardiovascular events. While substantial progress has been realized in clinical molecular imaging of plaques in larger arterial vessels (carotid, aorta, iliac), there remains a compelling, unmet need to develop molecular imaging strategies targeted to high-risk plaques in human coronary arteries. We present recent developments in intravascular near-IR fluorescence catheter-based strategies for in vivo detection of plaque inflammation in coronary-sized arteries. In particular, the biological, light transmission, imaging agent, and engineering principles that underlie a new intravascular near-IR fluorescence sensing method are discussed. Intravascular near-IR fluorescence catheters appear highly translatable to the cardiac catheterization laboratory, and thus may offer a new in vivo method to detect high-risk coronary plaques and to assess novel atherosclerosis biologics.
新的成像方法迫切需要在心肌梗死、中风和缺血性肢体发生之前识别出高风险的动脉粥样硬化病变。分子成像为可视化与心血管事件相关的高风险斑块的关键生物学特征提供了一种新方法。虽然在较大动脉血管(颈动脉、主动脉、髂动脉)的斑块临床分子成像方面已经取得了实质性进展,但仍然迫切需要开发针对人类冠状动脉高风险斑块的分子成像策略。我们介绍了用于活体检测冠状动脉大小的动脉中斑块炎症的基于近红外荧光导管的血管内策略的最新进展。特别是,讨论了新的血管内近红外荧光传感方法所依据的生物学、光传输、成像剂和工程原理。血管内近红外荧光导管似乎非常适合转化到心脏导管实验室,因此可能提供一种新的体内方法来检测高风险的冠状动脉斑块,并评估新的动脉粥样硬化生物标志物。