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放射性示踪剂解决心血管成像中的未满足临床需求,第 2 部分:炎症、纤维化、血栓形成、钙化和淀粉样变性成像。

Radiotracers to Address Unmet Clinical Needs in Cardiovascular Imaging, Part 2: Inflammation, Fibrosis, Thrombosis, Calcification, and Amyloidosis Imaging.

机构信息

Section of Cardiovascular Medicine, Yale University School of Medicine, New Haven, Connecticut.

Department of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, Connecticut; and.

出版信息

J Nucl Med. 2022 Jul;63(7):986-994. doi: 10.2967/jnumed.121.263507.

Abstract

Cardiovascular imaging is evolving in response to systemwide trends toward molecular characterization and personalized therapies. The development of new radiotracers for PET and SPECT imaging is central to addressing the numerous unmet diagnostic needs that relate to these changes. In this 2-part review, we discuss select radiotracers that may help address key unmet clinical diagnostic needs in cardiovascular medicine. Part 1 examined key technical considerations pertaining to cardiovascular radiotracer development and reviewed emerging radiotracers for perfusion and neuronal imaging. Part 2 covers radiotracers for imaging cardiovascular inflammation, thrombosis, fibrosis, calcification, and amyloidosis. These radiotracers have the potential to address several unmet needs related to the risk stratification of atheroma, detection of thrombi, and the diagnosis, characterization, and risk stratification of cardiomyopathies. In the first section, we discuss radiotracers targeting various aspects of inflammatory responses in pathologies such as myocardial infarction, myocarditis, sarcoidosis, atherosclerosis, and vasculitis. In a subsequent section, we discuss radiotracers for the detection of systemic and device-related thrombi, such as those targeting fibrin (e.g., Cu-labeled fibrin-binding probe 8). We also cover emerging radiotracers for the imaging of cardiovascular fibrosis, such as those targeting fibroblast activation protein (e.g., Ga-fibroblast activation protein inhibitor). Lastly, we briefly review radiotracers for imaging of cardiovascular calcification (F-NaF) and amyloidosis (e.g., Tc-pyrophosphate and F-florbetapir).

摘要

心血管成像正在发展,以响应向分子特征和个体化治疗的全系统趋势。用于正电子发射断层扫描(PET)和单光子发射计算机断层扫描(SPECT)成像的新型放射性示踪剂的开发是解决与这些变化相关的许多未满足的诊断需求的核心。在这两部分综述中,我们讨论了一些可能有助于解决心血管医学中关键未满足的临床诊断需求的放射性示踪剂。第 1 部分检查了与心血管放射性示踪剂开发相关的关键技术考虑因素,并审查了用于灌注和神经元成像的新兴放射性示踪剂。第 2 部分涵盖了用于成像心血管炎症、血栓形成、纤维化、钙化和淀粉样变性的放射性示踪剂。这些放射性示踪剂有可能解决与动脉粥样硬化风险分层、血栓检测以及心肌病的诊断、特征和风险分层相关的几个未满足的需求。在第 1 节中,我们讨论了针对心肌梗死、心肌炎、结节病、动脉粥样硬化和血管炎等疾病中炎症反应各个方面的放射性示踪剂。在接下来的一节中,我们讨论了用于检测系统性和器械相关血栓的放射性示踪剂,例如针对纤维蛋白的放射性示踪剂(例如,Cu 标记的纤维蛋白结合探针 8)。我们还介绍了用于成像心血管纤维化的新兴放射性示踪剂,例如针对成纤维细胞激活蛋白的放射性示踪剂(例如,Ga-成纤维细胞激活蛋白抑制剂)。最后,我们简要回顾了用于成像心血管钙化(F-NaF)和淀粉样变性(例如,Tc-焦磷酸盐和 F-氟脱氧葡萄糖)的放射性示踪剂。

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