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基质金属蛋白酶作为动脉粥样硬化斑块炎症活动的成像靶点。

Matrix-metalloproteinases as imaging targets for inflammatory activity in atherosclerotic plaques.

机构信息

European Institute for Molecular Imaging-EIMI, Münster, Germany.

出版信息

J Nucl Med. 2010 May;51(5):663-6. doi: 10.2967/jnumed.109.065698.

Abstract

Cardiovascular events such as myocardial infarction or stroke resulting from atherosclerosis still account for the majority of deaths worldwide. New imaging approaches focusing on the visualization of inflammation in the vessel wall may emerge as tools for individualized risk assessment and prevention of events. Enzymes such as matrix-metalloproteinases (MMPs) are involved in several steps in plaque progression driving plaques into vulnerable, rupture-prone states. Targeting of MMPs for imaging is therefore a promising strategy. The rationale, potential, and current status of imaging MMPs in the clinical context of stroke and myocardial infarction are reviewed here from a clinical viewpoint.

摘要

心血管事件,如动脉粥样硬化导致的心肌梗死或中风,仍然是全球范围内大多数死亡的原因。新的成像方法侧重于血管壁炎症的可视化,可能成为个体风险评估和预防事件的工具。酶如基质金属蛋白酶 (MMPs) 参与斑块进展的多个步骤,使斑块变得脆弱易破裂。因此,针对 MMPs 进行成像的靶向治疗是一种很有前途的策略。从临床角度来看,本文综述了 MMPs 在中风和心肌梗死临床背景下的成像的原理、潜力和现状。

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