Shim Chi Young, Lindner Jonathan R
Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR, USA.
Korean Circ J. 2014 Jan;44(1):1-9. doi: 10.4070/kcj.2014.44.1.1.
Methods for imaging the molecular or cellular profile of tissue are being developed for all forms of non-invasive cardiovascular imaging. It is thought that these technologies will potentially improve patient outcomes by allowing diagnosis of disease at an early-stage, monitoring disease progression, providing important information on patient risk, and for tailoring therapy to the molecular basis of disease. Molecular imaging is also already assuming an important role in science by providing a better understanding of the molecular basis of cardiovascular pathology, for assessing response to new therapies, and for rapidly optimizing new or established therapies. Ultrasound-based molecular imaging is one of these new approaches. Contrast-enhanced ultrasound molecular imaging relies on the detection of novel site-targeted microbubbles (MB) or other acoustically active particles which are administered by intravenous injection, circulate throughout the vascular compartment, and are then retained and imaged within regions of disease by ligand-directed binding. The technique is thought to be advantageous in practical terms of cost, time, and ease of use. The aim of this review is to discuss the molecular participants of cardiovascular disease that have been targeted for ultrasound imaging, general features of site-targeted MB, imaging protocols, and potential roles of ultrasound molecular imaging in cardiovascular research and clinical medicine.
针对所有形式的非侵入性心血管成像,正在开发用于对组织的分子或细胞特征进行成像的方法。人们认为,这些技术有可能通过在疾病早期进行诊断、监测疾病进展、提供有关患者风险的重要信息以及根据疾病的分子基础定制治疗方案来改善患者的治疗效果。分子成像通过更好地理解心血管病理学的分子基础、评估对新疗法的反应以及快速优化新的或已有的疗法,在科学领域也已经发挥着重要作用。基于超声的分子成像是这些新方法之一。对比增强超声分子成像依赖于检测新型的位点靶向微泡(MB)或其他声学活性颗粒,这些颗粒通过静脉注射给药,在血管腔内循环,然后通过配体导向结合在疾病区域内滞留并成像。从成本、时间和易用性等实际方面来看,该技术被认为具有优势。本综述的目的是讨论已被用于超声成像的心血管疾病的分子靶点、位点靶向微泡的一般特征、成像方案以及超声分子成像在心血管研究和临床医学中的潜在作用。